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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 864. Отображено 197.
01-01-1942 дата публикации

Способ получения метиленового голубого

Номер: SU61635A1
Принадлежит:

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27-11-1985 дата публикации

ORGANIC COMPOUNDS

Номер: GB0008525948D0
Автор:
Принадлежит:

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15-04-1981 дата публикации

VERFAHREN ZUR AUFTRENNUNG VON NUKLEINSAEUREN

Номер: ATA146078A
Автор:
Принадлежит:

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15-01-2009 дата публикации

WITH LIGHT (IN VIVO) COLORING COMPOSITION AND MANUFACTURING PROCESS STABILIZED

Номер: AT0000419016T
Принадлежит:

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13-03-1986 дата публикации

THERMAL IMAGING

Номер: AU0004651485A
Принадлежит:

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03-02-1976 дата публикации

CYANOVINYLENE-SUBSTITUTED TRIARYLAMINE, PHENOXAZINE AND PHENOTHIAZINE COMPOUNDS

Номер: CA0000983029A1
Принадлежит:

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12-04-1988 дата публикации

PHENOTHIAZINE AND PHENOXAZINE DERIVATIVES, PROCESS AND MARKING SYSTEMS

Номер: CA0001235124A1
Принадлежит:

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18-09-1973 дата публикации

RECORD MATERIAL AND MARKING LIQUID

Номер: CA933705A
Автор:
Принадлежит:

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12-04-1988 дата публикации

PHENOTHIAZINE AND PHENOXAZINE DERIVATIVES, PROCESS AND MARKING SYSTEMS

Номер: CA1235124A

PHENOTHIAZINE AND PHENOXAZINE DERIVATIVES PROCESSES AND MARKING SYSTEMS 3-(N-R2-N-Acylamino)-7-(N-R3-N-R4-amino)-10-acyl-phenothiazines and phenoxazines useful as color formers, particularly in electrochromic recording systems, are prepared by the interaction of the corresponding 3-(N-R2-amino)-7-(N-R3- N-R4-amino) phenothiazinium or phenoxazinium halide with a reducing agent to obtain the corresponding leuco compound and subsequently interacting the leuco compound with at least two molecular proportions of an acylating agent.

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18-09-1973 дата публикации

RECORD MATERIAL AND MARKING LIQUID

Номер: CA0000933705A1
Принадлежит:

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19-03-1985 дата публикации

PHENOTHIAZINE LEUCODYES FOR ELECTROCHROMIC RECORDING

Номер: CA0001184030A1
Принадлежит: NA

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06-02-2007 дата публикации

ACID-LABILE AND ENZYMATICALLY DIVISIBLE DYE COMPOUNDS FOR DIAGNOSIS WITH NEAR INFRARED LIGHT AND FOR THERAPY

Номер: CA0002287262C

The invention relates to acid-labile and enzymatically divisible compounds for in-vivo and in-vitro diagnosis by means of near infrared radiation (NIR-radiation), the use of said compounds as optic diagnostic and therapeutic agents, and the diagnostic agents containing said compounds.

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15-09-1976 дата публикации

Номер: CH0000579463A5
Автор:
Принадлежит: NCR CO, NCR CORP.

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14-11-1975 дата публикации

Номер: CH0000569050A5
Автор:
Принадлежит: CALBIOCHEM, CALBIOCHEM AG

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15-03-1977 дата публикации

Номер: CH0000585781A5
Автор:

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13-10-1978 дата публикации

Номер: CH0000605868A5

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15-04-1983 дата публикации

SULFONSAEUREGRUPPENFREIE BASIC COLORING MATERIALS, THEIR PRODUCTION AND USE.

Номер: CH0000635605A5
Принадлежит: SANDOZ AG

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29-04-1988 дата публикации

OXAZINVERBINDUNGEN, THEIR PRODUCTION AND USE.

Номер: CH0000665214A5
Автор: PEDRAZZI, REINHARD
Принадлежит: SANDOZ AG

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30-11-2013 дата публикации

Метод количественного определения гуминовых веществ в природных водах

Номер: MD0000004221C1

Изобретение относится к аналитической химии, а именно к фотоколориметрическому методу количественного определения гуминовых веществ в природных водах. Метод, согласно изобретению, состоит в том что добавляют водный раствор метиленового голубого к анализируемой пробе и измеряют разность поглощения света между исходным раствором метиленового голубого и полученной смесью при максимуме поглощения 609 нм. Концентрацию гуминовых веществ определяют используя калибровочную кривую. П. формулы: 1 ...

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30-09-2014 дата публикации

Способ определения водорастворимых гуминовых веществ в природных водах и твердых породах

Номер: MD0000004305B1

Изобретение относится к аналитической химии, а именно к способу определения водорастворимых гуминовых веществ в природных водах и твердых породах. Способ, согласно изобретению, включает экстракцию метанолом гуминовых веществ из сухого остатка воды или твердой породы, отделение охлажденного метанольного экстракта от твердой фазы декантацией, промывку твердой фазы метанолом, смешивание жидкой фазы полученной вследствие промывки с первичным метанольным экстрактом, упаривание полученной смеси до сухого вещества, приливание к сухому веществу точного объема водного раствора метиленового голубого. Концентрацию гуминовых веществ определяют по разности поглощения света между растворами метиленового голубого и ассоциата метиленового голубого с гуминовыми веществами при длине волны 609…611 нм. П. формулы: 1 Фиг.: 9 ...

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29-02-2012 дата публикации

Способ полной деструкции Метиленового синего в сточных водах с его повышенным содержанием

Номер: MD0000000484Y

Изобретение относится к способам удаления красителей из сточных вод, а именно к способу полной деструкции Метиленового синего в сточных водах с его повышенным содержанием. Способ, согласно изобретению, включает каталитическое окисление Метиленового синего при его концентрации не менее 120 мг/л путем барботирования кислорода при температуре 50…70°С и давлении газа 2 атм, в течение 2…3 часов, причем в качестве катализатора используется активированный уголь, полученный из скорлупы грецкого ореха с содержанием щелочных функциональных групп 0,555 мг-эквив./г и площадью мезопор 410 м2/г, при соотношении между катализатором и Метиленовым синим 50:3. Результат состоит в полной деструкции красителя с образованием простых компонентов - сульфатов, свободного азота, углекислого газа и воды, которые не токсичны. П. формулы: 1 Фиг.: 4 ...

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30-04-2015 дата публикации

Способ определения водорастворимых гуминовых веществ в природных водах и твердых породах

Номер: MD0000004305C1

Изобретение относится к аналитической химии, а именно к способу определения водорастворимых гуминовых веществ в природных водах и твердых породах. Способ, согласно изобретению, включает экстракцию метанолом гуминовых веществ из сухого остатка воды или твердой породы, отделение охлажденного метанольного экстракта от твердой фазы декантацией, промывку твердой фазы метанолом, смешивание жидкой фазы полученной вследствие промывки с первичным метанольным экстрактом, упаривание полученной смеси до сухого вещества, приливание к сухому веществу точного объема водного раствора метиленового голубого. Концентрацию гуминовых веществ определяют по разности поглощения света между растворами метиленового голубого и ассоциата метиленового голубого с гуминовыми веществами при длине волны 609…611 нм. П. формулы: 1 Фиг.: 9 ...

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30-09-2006 дата публикации

Дезинфицирующее средство

Номер: MD0000003145F1

Изобретение относится к медицине и фармацевтике и может быть использовано для дезинфекции медицинского оборудования и тканей. Сущность изобретения заключается в том что, заявленное дезинфицирующее средство содержит клатрат дидецилметиламонийбромид мочевина, 96°-й этиловый или изопропиловый спирт, метиленовую синь, эвкалиптовое масло, дистиллированную воду в следующем компонентном соотношении в масс. %: клатрат дидецилметиламонийбромид-мочевина 10,00…20,00 изопропиловый или 96°-йэтиловый спирт 9,50…10,50 метиленовая синь 0,0005…0,0020 эвкалиптовое масло 2,50…4,00 дистиллированную воду остальное П. формулы: 1 ...

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21-01-1983 дата публикации

ADSORBENT FOR SEPARATING SPECIFIC AFFINITY MACROMOLECULAR BODY, METHOD FOR ITS MANUFACTURE AND ITS APPLICATION

Номер: FR0002416721B1
Автор:
Принадлежит:

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02-10-1970 дата публикации

Cytologic dye for staining microscope sam- - ples

Номер: FR0002027498A5
Автор:
Принадлежит:

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07-09-1979 дата публикации

ADSORBENT FOR SEPARATING SPECIFIC AFFINITY MACROMOLECULAR BODY, METHOD FOR ITS MANUFACTURE AND ITS APPLICATION

Номер: FR0002416721A1
Автор:
Принадлежит:

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15-03-1984 дата публикации

MEANS FOR SOWING SEED DESINFECTION

Номер: BG0000035196A1
Принадлежит:

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10-10-1989 дата публикации

Oxazine-ureas and thiazine urea chromophors

Номер: US0004873318A1
Автор: Theodoropulos; Spyros
Принадлежит:

Novel adducts of oxazine urea chromophors or thiazine urea chromophors with organic substrates are provided which are useful in analytical techniques for the detection and measurement of biological and clinical compounds of interest.

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12-09-1989 дата публикации

Photohardenable compositions containing a dye-borate complex and photosensitive materials employing the same

Номер: US0004865942A1
Принадлежит: The Mead Corporation

A photohardenable composition comprising a free radical addition polymerizable or crosslinkable compound and a cationic dye-borate anion complex, said complex being capable of absorbing actinic radiation and producing free radicals which initiate free radical polymerization or crosslinking of said compound; and photosensitive materials employing the composition where in one embodiment the composition is microencapsulated.

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23-03-2021 дата публикации

Methods, systems, and apparatus for the monitoring, controlling, and communicating of electronic devices

Номер: US0010958308B2

Methods, systems, and apparatus for monitoring and controlling electronic devices using wired and wireless protocols are disclosed. The systems and apparatus may monitor their environment for signals from electronic devices. The systems and apparatus may take and disambiguate the signals that are received from the devices in their environment to identify the devices and associate control signals with the devices. The systems and apparatus may use communication means to send control signals to the identified electronic devices. Multiple apparatuses or systems may be connected together into networks, including mesh networks, to make for a more robust architecture.

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13-08-1987 дата публикации

BENZTHIAZINOPHENOXAZINE DYESTUFFS

Номер: DE0003464622D1
Принадлежит: BAYER AG

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16-07-1975 дата публикации

METHOD FOR THE PRODUCTION OF POLYCHROMATICALLY ACTIVE THIAZINE- COSINATES

Номер: GB0001400897A
Автор:
Принадлежит: Calbiochem Corp

1400897 Eosinate stain CALBIOCHEM AG 12 July 1973 [12 July 1972] 33387/73 Heading G1B [Also in Divisions C4 and G2] Eosinates of monomethylthionine dimethylthionine or a mixture may be used to stain haematological and bacteriological smears in a very short time (e.g. 30 seconds). Conventional additives may be used to enhance the coloration of the smears. Even coloration may be achieved by contacting a dry impregnated strip containing absorbed eosinate with an air-dried smear; filter paper is the preferred absorptive material.

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18-06-1980 дата публикации

Azo compounds

Номер: GB0002035352A
Автор: Long, William Edward
Принадлежит:

Novel azo compounds of the general formula:- (E)n@(A)n@ - (R1)n@ - N = N - BAL where A is a charged group which may be positively or negatively charged, E is a counter ion which carries a charge of opposite sign to that carried by A, BAL represents a ballasting group attached to the azo group via an aromatic or heterocyclic ring which may be further substituted, and R1 is an optionally substituted aromatic or heterocyclic group, and n1 is 1 or 2, n2 is 1 or 2 and n3 is 0 or 1 are used in diffusion transfer colour photographic materials. Example: A dyestuff of the formula:- ...

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16-09-1981 дата публикации

ADSORBENT FOR THE AFFINITY-SPECIFIC SEPARATION OF MACROMOLECULAR MATERIALS

Номер: GB0001597891A
Автор:
Принадлежит:

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15-10-1996 дата публикации

ANTIVIRAL THERAPY USING THIAZIN AND XANTHENFARBSTOFFEN

Номер: AT0000143596T
Принадлежит:

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06-12-1994 дата публикации

HEAT SENSITIVE RECORDING ELEMENT AND A THERMOGRAPHIC METHOD

Номер: CA0001333398C
Принадлежит: POLAROID CORP, POLAROID CORPORATION

A thermal imaging method for forming color images is provided which employs as the color imageforming material, a colorless precursor of a preformed image dye possessing at least one thermal protecting group that undergoes fragmentation upon heating and at least one leaving group that undergoes irreversible elimination upon heating, said protecting and leaving groups maintaining the precursor in its colorless form until heat is applied to effect removal of these groups whereby the precursor is converted to an image dye.

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24-08-2017 дата публикации

ANTINUCLEATING AGENTS FOR LASER SINTER POWDERS

Номер: CA0003012952A1
Принадлежит:

The present invention relates to a method for producing molded bodies by the selective laser sintering of a sintering powder (SP) which contains a polyamide (P) and 0.1 to 5 wt% of at least one additive (A). Moreover, the present invention relates to molded bodies which contain polyamide (P) and 0.1 to 5 wt% of at least one additive (A). Furthermore, the present invention relates to the production of sintering powders (SP) containing polyamide (P) and 0.1 to 5 wt% of at least one additive (A).

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17-07-1990 дата публикации

LIGHT-SENSITIVE COMPOSITION

Номер: CA0002007996A1
Принадлежит:

A light-sensitive composition is provided comprising (a) an aromatic diazo compound and (b) a cationic dye/borate anion complex. In a preferred embodiment, the cationic dye/anionic borate dye complex is represented by the general formula (I): ( I) wherein D+ represents a cationic dye; and R1, R2, R3 and R4, which may be the same or different, each represents an unsubstituted or substituted alkyl group, an unsubstituted or substituted aryl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkenyl group, an unsubstituted or substituted alkynyl group, an unsubstituted or substituted alicyclic group, or an unsubstituted or substituted heterocyclic group. The aromatic diazo compound can be a nonionic diazo compound. The light-sensitive compound can further comprise a radical-polymerizable unsaturated compound.

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13-05-1999 дата публикации

IN VIVO STAIN COMPOSITION, PROCESS OF MANUFACTURE, AND METHODS OF USE TO IDENTIFY DYSPLASTIC TISSUE

Номер: CA0002250731A1
Принадлежит:

The N-demethylation and N,N-demethylation derivatives of the two conformational isomers toluidine blue O ("TBO") have been synthesized, isolated and identified. An in vivo biological stain composition includes the conformational isomers of TBO and these N- and N,N-demethylation derivatives. The ratio of these isomers to these demethylation derivatives is at least 6:1. An improved method for detecting dysplastic oral tissue includes application of such TBO products, in a liquid carrier, to oral tissue. A process for preparing TBO products includes (1) oxidizing N,N-dimethyl-p-phenylenediamine to form an intermediate 2-amino-5-dimethylaminophenyl thiosulfonic acid, (2) oxidizing this intermediate and condensing the oxidizate with o-toluidine, forming indamine thiosulfonic acid and (3) further oxidizing the indamine intermediate to form a TBO-containing reaction product, which is precipitated from the reaction mixture as a complex, from which the final TBO product is separated. The complexing ...

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31-01-2010 дата публикации

Способ очистки сточных вод от метиленовой сини

Номер: MD0000004008B1

Изобретение относится к способам удаления органических красителей из сточных вод, в частности к способу очистки сточных вод от метиленовой сини. Способ включает каталитическое окисление путем барботирования кислорода в воде при температуре 30…50°С и давлении газа 2 атм в течение 2 часов, где в качестве катализатора используют активированный уголь, полученный из скорлупы грецкого ореха, с содержанием основных функциональных групп 0,555 мг экв/г и поверхностью переходных пор 410 м2/г. П. формулы: 1 ...

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30-04-2013 дата публикации

Метод количественного определения гуминовых веществ в природных водах

Номер: MD0000004221B1

Изобретение относится к аналитической химии, а именно к фотоколориметрическому методу количественного определения гуминовых веществ в природных водах. Метод, согласно изобретению, состоит в том что добавляют водный раствор метиленового голубого к анализируемой пробе и измеряют разность поглощения света между исходным раствором метиленового голубого и полученной смесью при максимуме поглощения 609 нм. Концентрацию гуминовых веществ определяют используя калибровочную кривую. П. формулы: 1 ...

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30-09-2010 дата публикации

Способ очистки сточных вод от метиленовой сини

Номер: MD0000004008C2

Изобретение относится к способам удаления органических красителей из сточных вод, в частности к способу очистки сточных вод от метиленовой сини. Способ включает каталитическое окисление путем барботирования кислорода в воде при температуре 30…50°С и давлении газа 2 атм в течение 2 часов, где в качестве катализатора используют активированный уголь, полученный из скорлупы грецкого ореха, с содержанием основных функциональных групп 0,555 мг экв/г и поверхностью переходных пор 410 м2/г. П. формулы: 1 Фиг.: 1 ...

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30-09-2012 дата публикации

Способ полной деструкции Метиленового синего в сточных водах с его повышенным содержанием

Номер: MD0000000484Z

Изобретение относится к способам удаления красителей из сточных вод, а именно к способу полной деструкции Метиленового синего в сточных водах с его повышенным содержанием. Способ, согласно изобретению, включает каталитическое окисление Метиленового синего при его концентрации не менее 120 мг/л путем барботирования кислорода при температуре 50…70°С и давлении газа 2 атм, в течение 2…3 часов, причем в качестве катализатора используется активированный уголь, полученный из скорлупы грецкого ореха с содержанием щелочных функциональных групп 0,555 мг-эквив./г и площадью мезопор 410 м2/г, при соотношении между катализатором и Метиленовым синим 50:3. Результат состоит в полной деструкции красителя с образованием простых компонентов - сульфатов, свободного азота, углекислого газа и воды, которые не токсичны. П. формулы: 1 Фиг.: 4 ...

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30-04-2007 дата публикации

Дезинфицирующее средство

Номер: MD0000003145G2

Изобретение относится к медицине и фармацевтике и может быть использовано для дезинфекции медицинского оборудования и тканей. Сущность изобретения заключается в том что, заявленное дезинфицирующее средство содержит клатрат дидецилметиламонийбромид мочевина, 96° -й этиловый или изопропиловый спирт, метиленовую синь, эвкалиптовое масло, дистиллированную воду в следующем компонентном соотношении в масс. % клатрат дидецилметиламонийбромид-мочевина 10,00…20,00; изопропиловый или 96° -йэтиловый спирт 9,50…10,50; метиленовая синь 0,0005…0,0020; эвкалиптовое масло 2,50…4,00; дистиллированную воду остальное. П. формулы: 1 ...

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15-09-2002 дата публикации

КОМПОЗИЦІЇ БАРВНИКІВ IN VIVO, СПОСІБ ЇХ ВИРОБНИЦТВА, СПОСОБИ ВИКОРИСТАННЯ ДЛЯ ВИЗНАЧЕННЯ ДИСПЛАСТИЧНОЇ ТКАНИНИ, СПОСІБ АНАЛІЗУ МЕТОДОМ РХВТ

Номер: UA0000048969C2
Принадлежит: Зила, ИНК, US, Зіла, ІHК, US

Вдалося виділити, ідентифікувати та приготувати N-деметильовані та N,N-деметильовані похідні двох конформаційних ізомерів толуїдинового синього О (ТСО). Композиція in vivo біологічного барвника включає конформаційні ізомери ТСО, а також ці N- та N,N-деметильовані похідні. Відношення цих ізомерів до названих деметильованих похідних становить, принаймні, 6 : 1. Вдосконалений метод виявлення диспластичної внутрішньоротової тканини включає нанесення зазначених ТСО продуктів в рідкому носії на внутрішньоротові тканини. Процес приготування ТСО продуктів включає (1) окиснення N,N-диметил- -фенілендіаміну з утворенням проміжного продукту - 2-аміно-5-диметиламінофеніл тіосульфокислоти, (2) окиснення цього проміжного продукту та конденсацію продукту окиснення -толуїдином з утворенням індамін тіосульфокислоти та (3) подальше окиснення індамінового проміжного продукту з утворенням продукту реакції, що містить ТСО, який осаджують з реакційної суміші як комплекс, з котрого виділяють кінцевий ТСО продукт ...

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26-08-1999 дата публикации

IN VIVO STAIN COMPOSITION, PROCESS OF MANUFACTURE, AND METHODS OF USE TO IDENTIFY DISPLASTIC TISSUE

Номер: EA0199800921A2
Автор: BURKETT DOUGLAS D
Принадлежит:

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24-12-2001 дата публикации

КОМПОЗИЦИЯ ДЛЯ ОКРАШИВАНИЯ IN VIVO, СПОСОБ ЕЕ ПОЛУЧЕНИЯ И СПОСОБЫ ЕЕ ПРИМЕНЕНИЯ ДЛЯ ИДЕНТИФИКАЦИИ ДИСПЛАСТИЧЕСКОЙ ТКАНИ

Номер: EA0000002127B1
Принадлежит: ЗИЛА, ИНК.

... 1. Композиция продукта толуидинового синего 0 (ТВО), отличающаяся тем, что соотношение суммарных площадей пиков ВЭЖХ при 254 нм, представляющих конформационные изомеры толуидинового синего 0, и суммарных площадей пиков, представляющих N-деметилированные производные указанных изомеров, составляет, по крайней мере, приблизительно 6:1. 2. Композиция продукта толуидинового синего 0 (ТВО), отличающаяся тем, что соотношение суммарных площадей пиков ВЭЖХ при 254 нм, представляющих первую группу компонентов, включающую конформационный изомер толуидинового синего 0, имеющий кольцевую метильную группу в положении 2, его N-деметилированное производное и его N,N-деметилированное производное, и суммарных площадей пиков ВЭЖХ, представляющих вторую группу компонентов, включающую конформационный изомер толуидинового синего 0, имеющий кольцевую метильную группу в положении 4, его N-деметилированное производное и его N,N-деметилированное производное составляет, по крайней мере, приблизительно 2,5:1. 3. Композиция ...

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28-09-1984 дата публикации

NOVEL DERIVATIVES OF 3:00-INDOLE ARE FREE FROM SULPHO GROUPS, USEFUL AS CATIONIC DYES

Номер: FR0002425465B1
Автор:
Принадлежит:

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02-09-1977 дата публикации

MATERIAL Of RECORDING

Номер: FR0002340210A1
Принадлежит:

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09-05-1980 дата публикации

DYES CONTAINING OF GROUPS AMINO OR IMINO

Номер: FR0002438672A1
Автор:
Принадлежит:

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23-07-2001 дата публикации

NEW HETEROCYCLIC COMPOUND

Номер: KR20010069206A
Принадлежит:

PURPOSE: A heterocyclic compound exhibiting excellent heat stability, light-resistance and high polymer-solubility when used in mass pigmentation of polar polymers such as a polyamide and a polyester and useful for a colorant is provided. CONSTITUTION: The compound is represented by formula(1) (R1 to R8 and R'5 to R'8 are each H, a halogen, hydroxy, NO2, CN, a C1-C12 alkyl, phenyl, naphthyl or the like). The compound represented by formula(1) can be obtained by reacting a compound represented by formula(3) (Hal is a halogen) with a compound represented by formula(4) (Met is Na+, K+ or Zn2+) and a compound represented by formula(5). For example, the violet powdery compound represented by formula(2) which has 383-385 deg.C of melting point is obtained by suspending 2,3-dichloronaphthoquinone in N,N-dimethylformamide and then adding and reacting 2-amino-5-chlorothiophenol therewith. Besides, the above polymer can be colored by adding and mixing an active amount of the colorant represented ...

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01-12-2005 дата публикации

FLUORESCENT METHOD AND COMPOUNDS TO MONITOR PROTEIN-LIPID BINDING

Номер: WO2005113524A1
Принадлежит:

The invention refers to compounds according to formula (I), wherein Rl is independently in position 2', 3', or in both positions of the A ring and is hydroxyl, linear or branched -0-alkyl, wherein the alkyl group has 1-12 carbon atoms, preferably 3-8, more preferably 4 carbon atoms, -O-(alkyl)COOH wherein the alkyl group has 1-12 carbon atoms, preferably 3-8, more preferably 4 carbon atoms, -O-(aryl)COOH, -0-aryl, linear or branched -O-(CH2)m-CH(NH2)-COOH with m = 1-6, preferably m= 2-4, or any combination thereof; R4 is in position 8', 10', or 1 l' of the D ring of the compound and is H or (CH2)n -CH3 with n = 0-6, COOH, CN, or halogen, R5 and R6 independently are ethyl-, methyl-, H, or -(CH2)3 connected to position 8 or 10 of the D ring, and wherein provided that X is O, R2 is F, Cl, Br, I, H, CN, -CH=CH-alkyl, -C =- C-alkyl, aryl and R3 is F, Cl, Br, I, CN, -CH=CH-alkyl, -C = C-alkyl, aryl and provided that X is S, R2 and R3 independently are F, Cl, Br, I, H, CN, -CH=CH-alkyl, - C=C-alkyl ...

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24-09-2009 дата публикации

STABILIZER FOR COLOR DEVELOPER AND USE THEREOF

Номер: WO000002009116575A1
Принадлежит:

Disclosed is a stabilizer which is capable of stabilizing 10-(carboxymethylaminocarbonyl)-3,7-bis(dimethylamino)phenothiazine salt or a derivative thereof even in the presence of moisture or under light irradiation. Specifically, at least one of compounds (1) and (2) described below is used as a stabilizer for 10-(carboxymethylaminocarbonyl)-3,7-bis(dimethylamino)phenothiazine salt or a derivative thereof. (1) a surfactant having an alkyl group with 8-16 carbon atoms (3) at least one dye material selected from the group consisting of compounds represented by formula (I), compounds represented by formula (II) and flavonoid dyes. R1-N=N-R2 (I) ...

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05-02-1991 дата публикации

Triphendioxazine and triphendithiazine direct dyestuffs

Номер: US0004990615A1
Принадлежит: Bayer Aktiengesellschaft

Triphendioxazine and triphendithiazine direct dyestuffs of the formula см. иллюстрацию в PDF-документе in which the substituents have the meanings given in the description produce on natural and synthetic OH-- and NH-- containing materials clear blue dyeings having good light and wet properties.

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28-07-2020 дата публикации

Redundant power line control systems

Номер: US0010727903B2

Methods, systems, and apparatus for monitoring and controlling electronic devices using wired and wireless protocols are disclosed. The systems and apparatus may monitor their environment for signals from electronic devices. The systems and apparatus may take and disambiguate the signals that are received from the devices in their environment to identify the devices and associate control signals with the devices. The systems and apparatus may use communication means to send control signals to the identified electronic devices. Multiple apparatuses or systems may be connected together into networks, including mesh networks, to make for a more robust architecture.

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15-07-1980 дата публикации

Process for preparing methylene blue

Номер: US0004212971A
Автор:
Принадлежит:

Methylene Blue and the zinc chloride double salt thereof are prepared by using manganese dioxide as the oxidizing agent in the substantial absence of toxic dichromates.

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12-07-2001 дата публикации

Process for manufacture of in vivo stain composition

Номер: US2001007904A1
Автор:
Принадлежит:

A process for synthesizing 2-amino-5-dimethlyaminophenyl thiosulfonic acid comprises the step of oxidizing N,N'-dimethyl-rho-phenylene-diamine in the presence of a source of thiosulfate ions, while maintaining the temperature of the reaction mixture not higher than about 10° C. This compound is useful as an intermediate in the synthesis of toluidine blue O. A process for manufacturing toluidine blue O with improved yield, includes the step of preparing the intermediate 2-amino-5-diethylaminopropyl thiosulfonic acid according to the above described procedure.

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05-09-2023 дата публикации

Methods and systems for wireless to power line communications

Номер: US0011751471B2
Автор: Phillip Bogdanovich
Принадлежит: Crius Technology Group, Inc.

Methods, systems, and apparatus for monitoring and controlling electronic devices using wired and wireless protocols are disclosed. The systems and apparatus may monitor their environment for signals from electronic devices. The systems and apparatus may take and disambiguate the signals that are received from the devices in their environment to identify the devices and associate control signals with the devices. The systems and apparatus may use communication means to send control signals to the identified electronic devices. Multiple apparatuses or systems may be connected together into networks, including mesh networks, to make for a more robust architecture.

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03-08-1999 дата публикации

STAINING COMPOSITION IN VIVO FOR CONFIRMING MALFORMED TISSUE, ITS PRODUCTION AND ITS USAGE

Номер: JP0011209357A
Автор: BURKETT DOUGLAS D
Принадлежит:

PROBLEM TO BE SOLVED: To obtain a stable-quality staining composition with high toluidine blue-O proportion, to provide a method for producing the composition, also to provide a method for confirming malformed tissue using the composition, and to provide a method for analyzing the composition. SOLUTION: This method for producing the subject staining composition comprises oxidation of N,N-dimethyl-p-phenylenediamine to form 2-amino-5- dimethylaminophenylthiosulfonic acid followed by its oxidation and then condensation reaction with o-toluidine to form indaminethiosulfonic acid which, in turn, is oxidized to effect cyclization of the indamine ring to produce a reaction product containing toluidine blue-O(TBO); wherein, prior to forming the reaction product, a complexing reagent is introduced into the system. COPYRIGHT: (C)1999,JPO ...

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31-10-1940 дата публикации

СПОСОБ ПОЛУЧЕНИЯ МЕТИЛЕНОВОГО ГОЛУБОГО

Номер: SU58213A1
Принадлежит:

Подробнее
24-08-1972 дата публикации

Номер: DE0002122301A1
Автор:
Принадлежит:

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08-10-2009 дата публикации

Ophthalmologisches Implantat, Mikroskopiesystem und optisches Nachweisverfahren zur Detektion und/oder Identifikation eines ophthalmologischen Implantats

Номер: DE102008017592A1
Принадлежит:

Die Erfindung betrifft ein ophthalmologisches Implantat, insbesondere eine Intraokularlinse, mit mindestens einer Markierung (16) hergestellt mit mindestens einem Farbstoff, wobei der Farbstoff ein fluoreszierender Farbstoff mit einem Emissionsmaximum außerhalb des für den Menschen sichtbaren Lichtspektrums oder ein absorbierender Farbstoff mit einem Absorptionsmaximum außerhalb des für den Menschen sichtbaren Lichtspektrums ist, jeweils ohne die Lichttransmission des ophthalmologischen Implantats (10) im visuellen Spektralbereich wesentlich zu beeinflussen. Die Erfindung betrifft weiterhin ein Mikroskopiesystem und ein optisches Nachweisverfahren zur Detektion und/oder Identifikation des erfindungsgemäßen ophthalmologischen Implantats (10).

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08-11-1961 дата публикации

Silicon-containing thiazine dyestuffs and a process for the preparation thereof

Номер: GB0000882064A
Автор:
Принадлежит:

The invention comprises silicon-containing thiazine dyestuffs of the general formula where Z is either (a) -XN-CaH2a-SiV3, wher X is hydrogen or alkyl or a CaH2a-SiV3 radical, or (b) -X11N-CaH2a-Si V Vb O 3-b/2, where X11 is hydrogen or alkyl or a CaH2a Si VbO 3-b/2 radical, b is 0, 1 or 2, and in both cases a is at least 3 and V is an alkyl group; R is hydrogen, alkyl or alkoxy, R1 is hydrogen, alkyl, alkoxy or sulpho, R11 is hydrogen or alkyl, and An is an anion of a mineral acid. They are prepared by oxidizing a mixture of a p-aminoaniline, an arylaminoalkylsilane and a metal thiosulphate, with a mineral acid solution of an alkali metal dichromate in the presence of zinc chloride. The arylaminoalkylsilane starting materials are disclosed in Specification 882,052. The silane dyestuffs are obtained when the starting silane contains no hydrolysable group. When hydrolysable groups are present, the dyestuffs are siloxanes. Suitable p-aminoanilines are p-phenylenediamine ...

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10-11-1981 дата публикации

PROCEDURE FOR ISOLATING OF NUCLEIC ACIDS

Номер: AT0000364734B
Автор:
Принадлежит:

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15-04-1981 дата публикации

PROCEDURE FOR ISOLATING OF NUCLEIC ACIDS

Номер: AT0000146078A
Автор:
Принадлежит:

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07-06-1999 дата публикации

(in vivo) stain composition, process of manufacture, and methods of use to identify dysplastic tissue

Номер: AU0005357498A
Принадлежит:

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21-06-2012 дата публикации

METHOD FOR PRESERVING AQUEOUS SOLUTION CONTAINING LEUCO CHROMOGEN

Номер: CA0002819045A1
Автор: SOYA, HARUYO, SOYA HARUYO
Принадлежит:

Disclosed are: a method for storing a leuco chromogen-containing aqueous solution, which is characterized by adding a compound that contains at least one substituent selected from the group consisting of a nitroso group and an azo group and has metal ion coordination ability or a salt of the compound to a leuco chromogen-containing aqueous solution; a method for stabilizing a leuco chromogen, which is characterized in that a leuco chromogen is made to coexist in an aqueous solution that contains a compound that contains at least one substituent selected from the group consisting of a nitroso group and an azo group and has metal ion coordination ability or a salt of the compound; and a liquid reagent which contains a leuco chromogen and a compound that contains at least one substituent selected from the group consisting of a nitroso group and an azo group and has metal ion coordination ability or a salt of the compound.

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12-11-1990 дата публикации

ANTIVIRAL THERAPY USING THIAZINE AND XANTHENE DYES

Номер: CA0002055463A1
Принадлежит:

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09-09-1990 дата публикации

PHOTOINITIATOR COMPOSITIONS CONTAINING DISULFIDES AND PHOTOHARDENABLE COMPOSITIONS CONTAINING THE SAME

Номер: CA0002009652A1
Принадлежит:

Photoinitiator compositions comprising a compound which absorbs actinic radiation and directly or indirectly generates free radicals and a disulfide compound are disclosed. The photointiator compositions have reduced sensitivity to oxygen and are preferably used in association with photographic imaging systems containing photosensitive microcapsules. Particularly preferred absorber compounds are ionic dye-counter ion complexes.

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14-03-2006 дата публикации

IN VIVO STAIN COMPOSITION, PROCESS OF MANUFACTURE, AND METHODS OF USE TO IDENTIFY DYSPLASTIC TISSUE

Номер: CA0002250731C

The N-demethylation and N,N-demethylation derivatives of the two conformational isomers toluidine blue O ("TBO") have been synthesized, isolated and identified. An in vivo biological stain composition includes the conformational isomers of TBO and these N- and N,N-demethylation derivatives. The ratio of these isomers to these demethylation derivatives is at least 6:1. An improved method for detecting dysplastic oral tissue includes application of such TBO products, in a liquid carrier, to oral tissue. A process for preparing TBO products includes (1) oxidizing N,N-dimethyl-p-phenylenediamine to form an intermediate 2-amino-5-dimethylaminophenyl thiosulfonic acid, (2) oxidizing this intermediate and condensing the oxidizate with o-toluidine, forming indamine thiosulfonic acid and (3) further oxidizing the indamine intermediate to form a TBO-containing reaction product, which is precipitated from the reaction mixture as a complex, from which the final TBO product is separated. The complexing ...

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13-04-1984 дата публикации

COMPOSITION, DEVICE AND METHOD FOR DETERMINING REDUCING AGENTS

Номер: FR0002400203B1
Автор:
Принадлежит:

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12-12-2018 дата публикации

전자 소자용 화합물

Номер: KR0101928714B1
Принадлежит: 메르크 파텐트 게엠베하

... 본 발명은 하기 화학식 (I) 에 따른 화합물, 유기 전자 소자에서의 이의 용도, 및 바람직하게는 정공 수송 물질 및/또는 특히 추가의 매트릭스 물질과 조합으로 매트릭스 물질로서의 화학식 (I) 에 따른 화합물을 함유하는 유기 전자 소자에 관한 것이다.

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15-08-1978 дата публикации

PROCEDE DE FABRICATION DE L'AZURITE B,COLORANT DE MICROSCOPIE,PAR DEGRADATION OXYDATIVE MENAGEE DU BLEU DE METHYLENE

Номер: RO0000063783A2
Автор:
Принадлежит:

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15-06-1982 дата публикации

Adsorbent for the affinity-specific separation of macromolecular materials

Номер: US0004335226A
Автор:
Принадлежит:

Adsorbents are provided for the affinity-specific separation of macromolecular materials, particularly biopolymers, the adsorbents comprising a polymeric carrier on to which an affine residue for the macromolecular material is covalently bound, either directly or via polymeric spacer. Preferred affine residue is comprised of a specific complex formers which are base-specific and/or structure specific for the macromolecular material. The invention also provides novel complex formers comprising a certain dyestuff residues and processes for their preparation.

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09-01-1991 дата публикации

A HEAT SENSITIVE RECORDING ELEMENT AND A THERMOGRAPHIC METHOD

Номер: EP0000406333A1
Принадлежит:

A thermal imaging method for forming color images is provided which employs as the color image-forming material, a colorless precursor of a preformed image dye possessing at least one thermal protecting group that undergoes fragmentation upon heating and at least one leaving group that undergoes irreversible elimination upon heating, said protecting and leaving groups maintaining the precursor in its colorless form until heat is applied to effect removal of these groups whereby the precursor is converted to an image dye.

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17-05-1991 дата публикации

DYE-BRANCHED ALKYL BORATE PHOTOINITIATOR

Номер: JP0003116043A
Принадлежит:

PURPOSE: To increase the processing rate of a film by using a specified compd. at a photoinitiator. CONSTITUTION: A photosetting compsn. and a photosensitive material containing a cationic dye-borate negative ion complex is used. A photoinitiator expressed by formula I is used. In formula I, D+ is a cationic dye, R1 is a branched alkyl group, R2 to R4 are each selected from the group consisting of alkyl, aryl, alkaryl, allyl, aralkyl, alkenyl, alkynyl, alicyclic and satd. or unsatd. heterocyclic groups. Thereby, a high processing rate of a film can be obtd. COPYRIGHT: (C)1991,JPO ...

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29-03-2007 дата публикации

OXIDATIVE GAS INDICATION MATERIAL AND PACKING VESSEL WITH INDICATION MEANS

Номер: JP2007074971A
Автор: SHIMIZU NOBUTOSHI
Принадлежит:

PROBLEM TO BE SOLVED: To provide an oxidative gas indication material visibly detecting a minute amount of oxidative gases (typically, oxygen, carbon dioxide, sulfur dioxide and the like) invading into a package/a vessel qualitatively and quantitatively with an oxidation reduction pigment converted to a reductant having no trace of reducibility by using fermentation actions of baker's yeast, and a packing vessel with an indication means using the same. SOLUTION: The oxidative gas indication material comprises the oxidation reduction pigment and at least baker's yeast coexisting in a medium. The oxidation reduction pigment is converted to the reductant having no reducibility by the action of the baker's yeast in an anaerobic atmosphere and brought to visible detection of the oxidative gases in a package/vessel. In the packing vessel with the indication means, the oxidative gas indication material is installed at a position where the oxidative gases can invade and inside of the packing/vessel ...

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10-02-2015 дата публикации

ЦИКЛО-БИС[(1Z)-1-ИМИНО-2-МЕТИЛ-1Н-ИНДЕН-3-ИЛ-1,2,4-ТИАДИАЗОЛ-3,5-ДИАМИН], ОБЛАДАЮЩИЙ СВОЙСТВОМ КИСЛОТНОГО КРАСИТЕЛЯ ДЛЯ ШЕЛКА, ШЕРСТИ И КАПРОНА

Номер: RU2540865C1

Изобретение относится к химической промышленности, а именно к новому гетероциклическому соединению, представляющему собой цикло-бис[(1Z)-1-имино-2-метил-1H-инден-3-ил-1,2,4-тиадиазол-3,5-диамин]. Технический результат - соединение в качестве кислотного красителя для шелка, шерсти и капрона. 3 ил., 5 пр.

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17-02-2022 дата публикации

Process for the Purification of Methylene Blue

Номер: US20220049102A1
Принадлежит:

The present application provides method for producing methylene blue that includes the steps of providing a reaction mixture having one or more methylene blue intermediates; precipitating metal from the reaction mixture; and producing therefrom crude methylene blue. The crude may further be purified, resulting in methylene compounds having low impurities, preferably having a purity greater than about 97%, having Azure B impurity no greater than 2.5%, and/or a total metal content no greater than 77 ppm. Formulations containing such compounds are also provided. 1. A compound comprising methylene blue having a purity greater than about 97%.2. The compound of claim 1 , the methylene blue further having Azure B impurity no greater than 2.5%.3. The compound of claim 1 , the methylene blue further having total metal content no greater than 77 ppm.4. A method for producing methylene blue comprising:providing a reaction mixture comprising one or more methylene blue intermediates;precipitating metal from the reaction mixture; andproducing therefrom crude methylene blue.5. The method of claim 3 , comprising extracting a solvent from the reaction mixture claim 3 , wherein the step of precipitating the metal from the reaction mixture is performed during solvent extraction.6. The method of claim 5 , wherein solvent extraction is performed with the reaction mixture having a pH between about pH 9 and about pH 11.7. The method of claim 3 , wherein methylene blue crude is produced in-situ without isolation of any intermediate(s).8. The method of claim 3 , wherein providing the reaction mixture comprises:reacting N,N-dimethylaniline with sodium nitrite in hydrochloric acid to obtain an in-situ nitroso compound;reducing the in-situ nitroso compound in the presence of zinc and hydrochloric acid to get obtain in-situ p-amino dimethyl aniline;reacting the in-situ p-amino dimethyl aniline with sulfuric acid and zinc chloride in a presence of sodium thiosulfate pentahydrate, sodium ...

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01-05-2014 дата публикации

PERMANENT ATTACHMENT OF AGENTS TO SURFACES CONTAINING C-H FUNCTIONALITY

Номер: US20140121333A1
Автор: Locklin Jason J.
Принадлежит:

An embodiment of the present disclosure can include a compound, a structure bonded to the compound, and the like. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a dye or a pigment and the structure can be a fiber, hair, or another structure. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a fluorinated compound and the structure can be a counter top, metal, or the like. 1. A compound comprising:R1-(C═O)—R2-X—W, where R1 and R2 are independently selected from the group consisting of: a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aryl group, and a substituted or unsubstituted heteroaryl group; X is selected from the group consisting of: O, NR3, a substituted or unsubstituted alkyl group, a S group, a substituted or unsubstituted aryl group, and a substituted or unsubstituted heteroaryl group; wherein R3 is selected from the group consisting of: a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aryl group, and a substituted or unsubstituted heteroaryl group; and wherein W is a pigment or a dye.2. The compound of claim 1 , wherein one of R1 and R2 is a substituted or unsubstituted aryl group.3. The compound of claim 1 , wherein both of R1 and R2 is a substituted or unsubstituted aryl group.4. The compound of claim 1 , wherein one of R1 and R2 is a substituted or unsubstituted phenyl group.5. The compound of claim 1 , wherein both of R1 and R2 is a substituted or unsubstituted phenyl group.6. An article comprising:R1-(C(Struc)OH)—R2-X—W, where R1 and R2 are independently selected from the group consisting of: a substituted or unsubstituted aliphatic group, a substituted or unsubstituted aryl group, and a substituted or unsubstituted heteroaryl group; X is selected from the group consisting of: O, NR3, a substituted or unsubstituted alkyl group, a S group, a substituted or unsubstituted aryl group, ...

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18-03-2021 дата публикации

Near-infrared absorbers, near-infrared absorbing/blocking films, photoelectric devices, organic sensors, and electronic devices

Номер: US20210083199A1
Принадлежит: SAMSUNG ELECTRONICS CO LTD

In Chemical Formula 1, X1, X2, Y1, Y2, Ar, Ar1, and Ar2 are the same as defined in the detailed description.

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30-03-2017 дата публикации

Fluorescent Organic Light Emitting Elements Having High Efficiency

Номер: US20170092874A1
Принадлежит:

The present invention relates to organic light emitting elements, comprising thermally activated delayed fluorescence (TADF) emitters and/or hosts of formula 8. A light-emitting layer comprising the compound according to .9. An organic light emitting element claim 1 , comprising the compound of formula (I) according to .10. The organic light-emitting element according to claim 9 , comprising a light-emitting layer claim 9 , wherein the light-emitting layer comprises a host material and a guest material claim 9 , wherein the guest material comprises the compound of formula (I).11. The organic light-emitting element according to claim 9 , comprising a light-emitting layer claim 9 , wherein the light-emitting layer comprises a host material and a guest material claim 9 , wherein the host material comprises the compound of formula (I).12. The organic light-emitting element according to claim 9 , wherein the organic light-emitting element emits delayed fluorescence.13. A device selected from the group consisting of a electrophotographic photoreceptor claim 1 , photoelectric converter claim 1 , sensor claim 1 , dye laser claim 1 , solar cell device and organic light emitting element claim 1 , wherein the device comprises a compound according to .14. Use of the compound according to for generating delayed fluorescence emission. The present invention relates to organic light emitting elements, comprising thermally activated delayed fluorescence (TADF) emitters and/or hosts of formula (I), which have a sufficiently small energy gap between Sand T(ΔE) to enable up-conversion of the triplet exciton from Tto S. The organic light emitting elements show high electroluminescent efficiency.The development of OLED luminescent materials is an important issue and these materials have been classified into two major categories. The first is fluorescent materials, which can harvest only the singlet excitons (25%) that are generated by electrical excitation. The second is phosphorescent ...

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28-03-2019 дата публикации

METHOD FOR THE DETERMINATION OF A CONCENTRATION OF A POLYACRYLIC ACID IN AN AQUEOUS MEDIUM

Номер: US20190094192A1
Принадлежит: BASF SE

The present invention relates to a method for the determination of a concentration (C) of a polyacrylic acid (PAA) in an aqueous medium (AM) wherein the determination is performed photometrically in the presence of a dye (I). The present invention furthermore, relates to a method for the determination of a concentration (C) of a polyacrylic acid (PAA) in an aqueous medium (AM) wherein at least two different transmittance values are measured using at least two different wavelengths and wherein the at least two different transmittance values are analyzed to determine the concentration (C) of the polyacrylic acid (PAA). The present invention also relates to the use of a dye (I) for the determination of the concentration (C) of a polyacrylic acid (PAA). 114-. (canceled)16. The method according to claim 15 , wherein step b) and step c) are carried out simultaneously.17. The method according to claim 15 , wherein in step a3) the conductivity of the aqueous medium (AM) is <1000 μS/cm.18. The method according to claim 15 , wherein the electrolyte-containing aqueous medium (EAM) comprises at least one electrolyte selected from the group consisting of an alkaline metal salt claim 15 , an alkaline earth metal salt and mixtures thereof.19. The method according to claim 15 , wherein the electrolyte-containing aqueous medium (EAM) comprises from 0.001 to 10% by weight of the at least one electrolyte claim 15 , based on the total amount of the electrolyte-containing aqueous medium (EAM).20. The method according to claim 15 , wherein the aqueous medium (AM) comprises a residue of the at least one electrolyte.21. The method according to claim 20 , wherein the aqueous medium (AM) comprises from 0 to 70 ppmw of the at least one electrolyte claim 20 , based on the total weight of the aqueous medium (AM) and wherein the ppmw of the at least one electrolyte comprised in the aqueous medium (AM) are smaller than the % by weight of the at least one electrolyte comprised in the electrolyte- ...

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11-04-2019 дата публикации

ORGANIC ELECTROLUMINESCENT ELEMENT

Номер: US20190109285A1
Принадлежит: IDEMITSU KOSAN CO., LTD.

An organic electroluminescence device includes an anode, a cathode and an emitting layer, in which the emitting layer includes a first compound and a second compound and each of the first compound and the second compound is a compound emitting thermally activated delayed fluorescence. 1an anode;a cathode; andan emitting layer, whereinthe emitting layer comprises a first compound and a second compound, andeach of the first compound and the second compound is a compound emitting thermally activated delayed fluorescence.. An organic electroluminescence device, comprising: The present invention relates to an organic electroluminescence device.When a voltage is applied to an organic electroluminescence device (hereinafter, occasionally referred to as an organic EL device), holes are injected from an anode into an emitting layer and electrons are injected from a cathode into the emitting layer. The injected electrons and holes are recombined in an emitting layer to form excitons. Here, according to the electron spin statistics theory, singlet excitons and triplet excitons are generated at a ratio of 25%:75%. In the classification according to the emission principle, in a fluorescent EL device which uses emission caused by singlet excitons, the limited value of an internal quantum efficiency of the organic EL device is believed to be 25%. On the other hand, in a phosphorescent EL device which uses emission caused by triplet excitons, it has been known that the internal quantum efficiency can be improved up to 100% when intersystem crossing efficiently occurs from the singlet excitons.A technology for extending a lifetime of a fluorescent organic EL device has recently been improved and applied to a full-color display of a mobile phone, TV and the like. However, an efficiency of a fluorescent EL device is required to be improved.Based on such a background, a highly efficient fluorescent organic EL device using delayed fluorescence has been proposed and developed. For ...

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13-06-2019 дата публикации

METHOD FOR PRESERVING LEUCO CHROMOGEN-CONTAINING AQUEOUS SOLUTION

Номер: US20190177548A1
Автор: KATAYAMA Yuki, Soya Haruyo
Принадлежит:

The present invention provides a method for preserving a leuco chromogen-containing aqueous solution comprising: adding at least one acid compound selected from the group consisting of a phosphoric acid compound, a carboxylic acid compound, a sulfonic acid compound, and a sulfuric acid compound to a leuco chromogen-containing aqueous solution; a method for stabilizing a leuco chromogen in an aqueous solution comprising: adding at least one acid compound selected from the group consisting of a phosphoric acid compound, a carboxylic acid compound, a sulfonic acid compound, and a sulfuric acid compound to a leuco chromogen-containing aqueous solution; and a liquid reagent comprising a leuco chromogen and at least one acid compound selected from the group consisting of a phosphoric acid compound, a carboxylic acid compound, a sulfonic acid compound, and a sulfuric acid compound. 1. A method for preserving a leuco chromogen-containing aqueous solution comprising:adding at least one acid compound selected from the group consisting of a phosphoric acid compound, a carboxylic acid compound, a sulfonic acid compound, and a sulfuric acid compound to the leuco chromogen-containing aqueous solution.2. The method according to claim 1 , wherein the phosphoric acid compound is a compound selected from the group consisting of phosphoric acid claim 1 , alkyl phosphoric acid claim 1 , polyoxyethylene alkyl ether phosphoric acid claim 1 , polyoxyethylene polycyclic phenyl ether phosphoric acid claim 1 , and salts thereof3. The method according to claim 1 , wherein the carboxylic acid compound is a compound selected from the group consisting of polyoxyethylene alkyl ether fatty acid claim 1 , N-acylamino acid in which a hydrogen atom of the amino group may be substituted with a substituent claim 1 , and salts thereof.4. The method according to claim 1 , wherein the sulfonic acid compound is a compound selected from the group consisting of N-acyl taurine in which a hydrogen atom of the ...

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09-07-2015 дата публикации

Camouflage Pattern With Extended Infrared Reflectance Separation

Номер: US20150192392A1
Автор: Dale R. Wendel
Принадлежит: International Textile Group Inc

Fabrics containing camouflage patterns are produced from dyes wherein at least certain of the colors contained in the pattern contain a low reflectance dye. The low reflectance dye is added to one or more colors in the pattern in order to preserve the camouflage pattern when viewed through night vision goggles as relatively long wavelengths, such at wavelengths greater than 900 nm. In one embodiment, the low reflectance dye comprises a thiazine. The low reflectance dye is blended with other dyes to produce colors in the pattern. By altering the concentration of the low reflectance dye in each of the colors, the colors contained in the camouflage pattern remain separate and distinct even at relatively long wavelengths.

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20-06-2019 дата публикации

PROCESS FOR THE PREPARATION OF DIAMINOPHENOTHIAZINIUM COMPOUNDS HAVING A HIGH DEGREE OF PURITY

Номер: US20190185440A1
Принадлежит:

A process for the preparation of diaminophenothiazinium compounds is described, which allows achieving quickly and effectively a high degree of purity of the same. 2. The process of claim 1 , wherein said crude diaminophenothiazinium compound of formula A is crude Methylene blue claim 1 , Methylene Blue zinc double salt or a mixture thereof.3. The process of claim 1 , wherein step 3) is a one-pot synthesis step.4. The process of claim 1 , wherein said stable free radical agent is TEMPO claim 1 , NHAc-TEMPO claim 1 , 4-C1-6-alkyloxy-TEMPO claim 1 , 4-benzoxyloxy-TEMPO claim 1 , 4-methoxy-TEMPO claim 1 , 4-carboxylic-4-amino-TEMPO claim 1 , 4-chloro-TEMPO claim 1 , 4 hydroxylimine-TEMPO claim 1 , 4-hydroxy-TEMPO claim 1 , 4-oxo-TEMPO claim 1 , 4-oxo-TEMPO-ethylene ketal claim 1 , 4-amino-TEMPO claim 1 , 2 claim 1 ,2 claim 1 ,6 claim 1 ,6-tetraethyl-1-piperidinyloxy claim 1 , 2 claim 1 ,2 claim 1 ,6-trimethyl-6-ethyl 1-piperidinyloxy claim 1 , 1 claim 1 ,3 claim 1 ,3-trimethyl-2-azabicyclo[2 claim 1 ,2 claim 1 ,2]octane-5-one-2-oxide claim 1 , 1-azabicyclo[3 claim 1 ,3 claim 1 ,1]nonane-2-oxide claim 1 , 2-Azaadamantane N-Oxyl (AZADO) claim 1 , 9-Azabicyclo[3.3.1]nonane N-oxyl (ABNO) claim 1 , 9-Azanoradamantane N-oxyl (Nor-AZADO) claim 1 , or a mixture thereof.5. The process of claim 4 , wherein said stable free radical agent is TEMPO claim 4 , NHAc-TEMPO claim 4 , 4-methoxy-TEMPO claim 4 , 4-carboxylic-4-amino-TEMPO claim 4 , 4-chloro-TEMPO claim 4 , 4 hydroxylimine-TEMPO claim 4 , 4-hydroxy-TEMPO claim 4 , 4-oxo-TEMPO claim 4 , 4-amino-TEMPO claim 4 , 2-Azaadamantane N-Oxyl (AZADO) claim 4 , 9-Azabicyclo[3.3.1]nonane N-oxyl (ABNO) claim 4 , 9-Azanoradamantane N-oxyl (Nor-AZADO) claim 4 , or a mixture thereof.6. The process of claim 5 , wherein said stable free radical agent is TEMPO claim 5 , 4-hydroxy-TEMPO claim 5 , 2-Azaadamantane N-Oxyl (AZADO) claim 5 , or a mixture thereof.7. The process of claim 6 , wherein said stable free radical agent is 4-hydroxy-TEMPO.8. ...

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17-08-2017 дата публикации

Oral Sampling Swab And Uses Thereof

Номер: US20170231603A1
Принадлежит:

Oral sampling swab for visually assessing treatment effectiveness of an oral care product in decreasing the amount of bacteria in an oral cavity and method of use thereof. 1. An oral sampling swab for assessing treatment effectiveness of an oral care product in decreasing the amount of bacteria in an oral cavity , the oral sampling swab comprising:(a) a swab comprising a handle at one end for handling the swab, a swab head, and a hollow swab stem connecting the handle to the swab head to provide fluid passage of a dye stored in a receptacle inside the handle to the swab head, wherein the swab head is configured for obtaining a biological sample from an oral cavity, wherein the dye is configured to exhibit a visible color change upon reacting with bacteria contained in the obtained biological sample; and(b) a reaction tube comprising an upper open end and an opposing lower closed end, wherein the swab is removably inserted in the reaction tube such that at least the handle of the swab protrudes from the upper open end when the swab head abuts the lower closed end of the reaction tube.2. The oral sampling swab of wherein the receptacle further comprises a fragible spacer configured to contain the dye in the receptacle and release the dye from storage upon sufficient pressure applied to break the fragible spacer claim 1 , such that the dye passes from the receptacle through the hollow swab stem into the reaction tube.3. The oral sampling swab of wherein the dye is selected from the group consisting of 7-Hydroxy-3H-phenoxazin-3-one 10-oxide claim 1 , (3-(4 claim 1 ,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) claim 1 , (2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-(2 claim 1 ,4-disulfophenyl)-2H-tetrazolium) claim 1 , (2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2 claim 1 ,4-disulfophenyl)-2H-tetrazolium) claim 1 , 3-[4 claim 1 ,5-dimethylthiazol-2-yl]-2 claim 1 ,5-diphenyltetrazolium bromide claim 1 , 2 claim 1 ,3 claim 1 ,5- ...

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21-09-2017 дата публикации

PROCESS FOR THE PURIFICATION OF DIAMINOPHENOTHIAZINIUM COMPOUNDS

Номер: US20170267652A1
Автор: Eutick Malvin
Принадлежит:

A process for the purification of diaminophenothiazinium compounds, and particularly of methylene blue, is described. The process provides for simple and effective purification by reduction of the post-synthesis or commercially available diaminophenothiazinium compound to form a reduced complex thereof. This can then be purified in a more straightforward manner than the original compound by, for example, recrystallization before being allowed to oxidise back to the diaminophenothiazinium compound.

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05-09-2019 дата публикации

NOVEL OXIDATION COLOR DEVELOPABLE COMPOUND AND OXIDATION COLOR DEVELOPMENT REAGENT

Номер: US20190270888A1
Принадлежит: DOJINDO LABORATORIES

The present invention pertains to: an oxidation color developable compound that is represented by general formula (1), that has excellent solubility in water, and that is less affected by a substance coexisting in a sample; and an oxidation color development reagent using the oxidation color developable compound. In general formula (I), R, R, R, and Reach represent a straight-chain or branched alkyl group having 1-6 carbon atoms, X represents a hydrophilic functional group, and L represents —(CH)— (j represents an integer of 2-10), —(CHCHO)— (k represents an integer of 1-10), or —(CH)—Z—(CH)— (m and n each independently represent an integer of 1-10, and Z represents —N(CH)—, —CONH—, —NHCO—, —COO—, —OCO—, —NHCOO—, —OCONH—, —NHCONH—, and —(CHNHCO)—). 2: The oxidative chromogenic compound according to claim 1 , wherein the hydrophilic functional groups X represents —COO claim 1 , —SO claim 1 , β-cyclodextrin or γ-cyclodextrin.4: An oxidative chromogenic reagent comprising the oxidative chromogenic compound according to .5: The oxidative chromogenic reagent according to claim 4 , wherein the oxidative chromogenic reagent is to be used for measuring an oxidation reaction to which a peroxidase involves. The invention relates to improvement of oxidative chromogenic compounds and oxidative chromogenic reagents.In the field of clinical test, quantification of hydrogen peroxide has been carried out by using a reagent consisting of an oxidative chromogenic compound. For example, the oxidative chromogenic compound having phenothiazine structure as described in Patent Literature 1 (DA-67, FUJIFILM Wako Pure Chemicals corporation. see structural formula shown below) enables high sensitivity measurement because of its high molecular extinction coefficient.However, DA-67 has a drawback of low optical stability. In view of such problem, for example, a compound having adamantane skeleton of which structural formula is shown below has been proposed as an oxidative chromogenic compound ...

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27-08-2020 дата публикации

Passive Component for Detecting an Electrical Overload in Electrically Rotating Machines

Номер: US20200274428A1
Принадлежит: SIEMENS AKTIENGESELLSCHAFT

Various embodiments include a passive component comprising: a substrate; and two conductor tracks disposed on the substrate. The substrate forms an electrically insulating bridge between at least two phases of an electrically rotating machine. Each of the two conductor tracks is coupled to a separate phase of the at least two phases so an electrical potential across the electrically insulating bridge is the same as in the insulation system of the machine and the potential load on the passive component corresponds to the potential load on the insulation system. 1. A passive component comprising a substrate and at least two conductor tracks thereon in such a way that the substrate forms an electrically insulating bridge between at least two phases of an electrically rotating machine and the conductor tracks are each coupled to one phase in order that the electrical potential across the electrically insulating bridge is the same as in the insulation system of the machine , such that the potential load on the passive component corresponds to the potential load on the insulation system.2. The passive component as claimed in claim 1 , in the form of a test strip.3. The passive component as claimed in or claim 1 , provided in the terminal box of a motor.4. The passive component as claimed in any of the preceding claims claim 1 , wherein the conductor tracks are made of a composite material.5. The passive component as claimed in any of the preceding claims claim 1 , wherein the shape and position of the conductor tracks on the substrate is chosen such that no partial discharge via the conductor tracks of the passive component takes place at the operating voltage of the electrically rotating machine.6. The passive component as claimed in any of the preceding claims claim 1 , wherein the composite material comprises an epoxy resin filled at least up to the percolation threshold with electrically conductive filler.7. The passive component as claimed in claim 6 , wherein the ...

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24-10-2019 дата публикации

DYED LEATHER-LIKE SHEET AND FIBER STRUCTURE

Номер: US20190323173A1
Принадлежит: KURARAY CO., LTD.

Disclosed is a leather-like sheet having a lightness L* of 35 or less, and including a fiber structure including fiber dyed with a dye composition including C.I. Basic Blue 3 and at least one blue cationic dye other than C.I. Basic Blue 3, and an elastic polymer contained in internal voids of the fiber structure, or the fiber structure. Also disclosed is a leather-like sheet having a lightness L* of 35 or less, and including a fiber structure including fiber dyed with an azo-based blue cationic dye, and an elastic polymer contained in internal voids of the fiber structure, wherein the leather-like sheet or the fiber structure has a color difference (ΔE), determined when treated for 48 hours under moist and hot conditions of 80° C. and a moisture of 90%, of ΔE≤2. or the fiber structure 1: A leather-like sheet , comprising:a fiber structure dyed with a dye composition including C.I. Basic Blue 3, which is an oxazine-based blue cationic dye, and at least one blue cationic dye other than C.I. Basic Blue 3; andan elastic polymer contained in internal voids of the fiber structure,wherein the leather-like sheet has a lightness L* of 35 or less in a color coordinate space (L*a*b* color space).2: The leather-like sheet according to claim 1 , wherein the C.I. Basic Blue 3 is contained in an amount of 30 to 70 mass % relative to a total amount of C.I. Basic Blue and the at least one blue cationic dye other than C.I. Basic Blue 3.3: The leather-like sheet according to claim 1 , wherein the at least one blue cationic dye other than C.I. Basic Blue 3 includes an azo-based blue cationic dye.4: The leather-like sheet according to claim 3 , wherein the azo-based blue cationic dye includes at least one selected from the group consisting of C.I. Basic Blue 159 and C.I. Basic Blue 54.5: The leather-like sheet according to claim 3 , further comprising:an anionic polyhydric phenol derivative.6: The leather-like sheet according to claim 3 , wherein the at least one blue cationic dye other ...

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29-10-2020 дата публикации

CERIUM (III) CARBONATE FORMULATIONS

Номер: US20200339435A1
Принадлежит:

The disclosure provides, inter alia, formulations comprising cerium (III) carbonate, and processes for producing cerium (III) carbonate. In embodiments, the disclosure provides methods for passivating photodegradation of organic compounds using cerium (III) carbonate. 1. A composition comprising cerium (III) carbonate and a pigment or a dye or a combination thereof.2. The composition of claim 1 , which comprises a pigment selected from the group consisting of: titanium dioxide claim 1 , zinc oxide claim 1 , cerium oxide claim 1 , zirconium oxide claim 1 , tungsten oxide claim 1 , vanadium oxide claim 1 , tin oxide claim 1 , nickel oxide claim 1 , copper oxide claim 1 , molybdenum oxide claim 1 , tungsten sulfide claim 1 , cadmium sulfide claim 1 , cadmium selenide claim 1 , zinc sulfide claim 1 , calcium carbonate claim 1 , mica claim 1 , silicas claim 1 , talcs claim 1 , graphite claim 1 , white lead claim 1 , barium sulfate claim 1 , calcium carbonate claim 1 , lithopone claim 1 , silica claim 1 , talc claim 1 , mica claim 1 , clays claim 1 , calcined clays claim 1 , lead silico-chromate claim 1 , zinc chromate claim 1 , calcium zinc molybdate claim 1 , barium metaborate claim 1 , zinc oxide claim 1 , zinc sulfide claim 1 , or a combination thereof.3. The composition of claim 1 , wherein the composition comprises a pigment which is titanium dioxide.4. The composition of claim 1 , which comprises a dye selected from the group consisting of: iron oxide claim 1 , carbon black claim 1 , cadmium sulfide claim 1 , toluidene red claim 1 , chrome orange claim 1 , chrome yellow claim 1 , chrome green claim 1 , polyazaindacenes claim 1 , coumarins claim 1 , lanthanide complexes claim 1 , hydrocarbon and substituted hydrocarbon dyes claim 1 , polycyclic aromatic hydrocarbons claim 1 , scintillation dyes claim 1 , aryl- and heteroaryl-substituted polyolefins claim 1 , carbocyanine dyes claim 1 , phthalocyanine dyes and pigments claim 1 , oxazine dyes claim 1 , carbostyryl ...

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28-12-2017 дата публикации

METHOD FOR PREVENTION OF PREMATURE POLYMERIZATION

Номер: US20170369458A1
Принадлежит: NITTO EUROPE N.V.

The present invention relates to a method for prevention of premature polymerization during the preparation, purification, transportation and storage of a polymerizable compound with at least one conjugated unsaturated group in the presence of an azine dye-based compound as inhibitor. Further the present invention relates to methods of preparing such inhibitors as well as to the inhibitors itself, as well as to methods of improving solubility and stability of dissolved inhibitors. 2. The azine dye-based compound according to claim 1 , wherein n is an integer of from 7 to 20.3. The azine dye-based compound according to claim 2 , wherein X is selected from any of CH(CH)SO claim 2 , CH(CH)SO claim 2 , or CH(CH)SO.4. The azine dye-based compound according to claim 1 , wherein the organic sulfonate comprising an hydroxyl substituted aromatic moiety is 3-(2 claim 1 ,5-di-tert-butyl-4-hydroxy-phenoxy)-propane-1-sulfonate.5. A composition comprising a polymerizable compound with at least one conjugated unsaturated group and an azine dye-based compound according to .6. The composition according to claim 5 , wherein the azine dye-based compound is present in a concentration of 10 to 1000 ppm.7. The composition according to claims 5 , wherein the polymerizable compound with at least one conjugated unsaturated group is selected from acrylic acid claims 5 , methacrylic acid and esters thereof. The present application is a divisional patent application of U.S. patent application Ser. No.: 15/079,967, filed Mar. 24, 2016, which claims priority from European Patent Application No. 15000894.4, filed Mar. 26, 2015, the contents of all of which are herein incorporated by reference in their entirety.The present invention relates to a method for prevention of premature polymerization during the preparation, purification, transportation and storage of a polymerizable compound with at least one conjugated unsaturated group in the presence of an azine dye-based compound as inhibitor. ...

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05-12-2019 дата публикации

Electrolytic Solution, Electrolytic Aqueous Solution, and Power Generating Device

Номер: US20190372145A1
Принадлежит:

The present invention provides a method for suppressing generation of hydrogen gas at the time when an ion concentration gradient is generated by a temperature responsive electrolyte. An electrolytic solution contains a temperature responsive electrolyte and an oxidation-reduction active species. The temperature responsive electrolyte is an electrolyte whose pKa varies according to the temperature. A power generating device performs power generation by using the electrolytic solution. The power generating device includes a positive electrode, a negative electrode, a heating mechanism, and a cooling mechanism. The positive electrode and the negative electrode are immersed in the electrolytic solution. The heating mechanism heats the electrolytic solution that is present in the vicinity of one of the positive electrode and the negative electrode. The cooling mechanism cools the electrolytic solution that is present in the vicinity of the other one of the positive electrode and the negative electrode. 2. An electrolytic solution comprising:a temperature responsive electrolyte that is an electrolyte whose pKa varies according to temperature; andan oxidation-reduction active species selected from among N,N,N′,N′-tetramethyl-p-phenylenediamine or a derivative thereof, nicotinamide or a derivative thereof, a proflavine hemisulfate hydrate or a derivative thereof, riboflavin or a derivative thereof, sulfated anthraquinone or a derivative thereof, naphthoquinone or a derivative thereof, or methylene blue or a derivative thereof.38-. (canceled)9. The electrolytic solution according to claim 1 ,wherein the temperature responsive electrolyte is a molecule that has a polar group, a hydrophobic group, and an ionizable functional group.10. A power generating device that performs power generation by using the electrolytic solution according to claim 1 , the power generating device comprising:a positive electrode;a negative electrode;a heating mechanism; and wherein the positive ...

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22-12-1987 дата публикации

Novel oxazine-ureas and thiazine urea chromophors as fluorescent labels

Номер: US4714763A
Автор: Spyros Theodoropulos
Принадлежит: Viomedics Inc

Novel urea derivatives of oxazine and thiazine chromophors have the structural formula I or II. ##STR1## wherein M is oxygen or sulfur, R 1 and R 2 are aliphatic alkyl groups or hydrogen; R 3 is hydrogen or alkyl group; R 4 is hydrogen, alkyl or amine group; R 5 is hydrogen, amine or alkyl group; X.sup.⊖ is an anion consisting of an organic (e.g. CH 3 COO.sup.⊖, CH 3 CH 2 COO.sup.⊖ and the like) or inorganic specie (e.g. Cl.sup.⊖, Br.sup.⊖, I.sup.⊖, ClO 4 .sup.⊖, SO 4 ", and the like); n is 0 to 20; Z is N═C═O, N═C═S, carboxylic, primary or secondary amine, and when n=0, Z may be ##STR2## wherein Q is hydroxyl, amino, carboxylic, sulfydryl, isocyanato, or isothiocyanato. The functional oxazine-urea and thiazine-urea derivatives react with compounds of interest to form adducts resulting in the fluorescent labeling of the compound.

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09-07-1999 дата публикации

有機電界発光素子

Номер: JPH11185966A
Принадлежит: Mitsui Chemicals Inc

(57)【要約】 【解決手段】 一対の電極間に、一般式(1)で表され る化合物を少なくとも1種含有する層を少なくとも一層 挟持してなる有機電界発光素子。 (式中、Ar 1 〜Ar 7 は置換または未置換のアリール 基を表し、さらに、Ar 1 とAr 2 、Ar 3 とAr 4 お よびAr 5 とAr 6 は結合している窒素原子と共に含窒 素複素環を形成していてもよいを表し、R 1 およびR 2 は水素原子、直鎖、分岐または環状のアルキル基、置換 または未置換のアリール基、あるいはアラルキル基を表 し、Z 1 およびZ 2 は水素原子、ハロゲン原子、直鎖、 分岐または環状のアルキル基、アルコキシ基、あるいは 置換または未置換のアリール基を表す) 【効果】 発光寿命が長く、耐久性に優れた有機電界発 光素子を提供する。

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10-06-1975 дата публикации

Patent CS161675B2

Номер: CS161675B2
Автор: [UNK]
Принадлежит: [UNK]

Подробнее
06-12-2007 дата публикации

New materials for organic electroluminescent devices

Номер: DE102006025777A1
Принадлежит: Merck Patent GmBH

Die vorliegende Erfindung betrifft Verbindungen gemäß Formel (1) und deren Verwendung in organischen Elektrolumineszenzvorrichtungen, insbesondere als Matrixmaterial in phosphoreszierenden Vorrichtungen.

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19-09-2013 дата публикации

Electronic devices

Номер: WO2013135352A1
Принадлежит: Merck Patent GmBH

The application relates to an electronic device containing an anode, a cathode, at least one emitting layer between the anode and the cathode, at least one p-doped layer A which contains mono-triarylamine as host material, and at least one layer B containing mono-triarylamine. The invention further relates to a p-doped mixture containing mono-triarylamine of the formula (II), (III) or (IV) as host material and an electron acceptor compound as dopant and to the use of the mixture in an electronic device.

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05-06-2014 дата публикации

Electronic device

Номер: WO2014082705A1
Принадлежит: Merck Patent GmBH

The invention relates to an electronic device containing a heteroaromatic compound of formula (I) as a functional material, in particular as an electron transport material and as a matrix material for emitter compounds.

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08-12-2015 дата публикации

Materials for organic electroluminescent devices

Номер: US9206351B2
Принадлежит: Merck Patent GmBH

The present invention relates to compounds according to formula (1) and/or according to formulae (4) to (10) and their use in organic electroluminescent devices, in particular as a matrix material in phosphorescent devices.

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27-03-2019 дата публикации

Electronic devices

Номер: EP3460864A1
Принадлежит: Merck Patent GmBH

Die Anmeldung betrifft eine elektronische Vorrichtung enthaltend Anode, Kathode, mindestens eine emittierende Schicht zwischen Anode und Kathode, mindestens eine p-dotierte Schicht A, welche ein Mono-Triarylamin als Host enthält, sowie mindestens eine Schicht B enthaltend ein Mono-Triarylamin. Weiterhin betrifft die Erfindung eine p-dotierte Mischung enthaltend ein Mono-Triarylamin der Formel (II), (III) oder (IV) als Host und eine Elektronenakzeptorverbindung als Dotanden und die Verwendung der Mischung in einer elektronischen Vorrichtung. The application relates to an electronic device comprising anode, cathode, at least one emitting layer between the anode and cathode, at least one p-doped layer A, which contains a mono-triarylamine as a host, and at least one layer B containing a mono-triarylamine. Furthermore, the invention relates to a p-doped mixture containing a mono-triarylamine of the formula (II), (III) or (IV) as a host and an electron acceptor compound as dopants and the use of the mixture in an electronic device.

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01-06-2016 дата публикации

Measure the assay method of object component

Номер: CN103261434B
Автор: 村上智美
Принадлежит: Kyowa Medex Co Ltd

一种样品中的测定对象成分的测定方法,其特征在于,将样品中的测定对象成分转换成过氧化氢,在α-酮酸存在下,使用氧化发色型色原体测定所生成的过氧化氢。一种抑制过氧化物的影响的方法,其特征在于,在将样品中的测定对象成分转换成过氧化氢、使用氧化发色型色原体测定所生成的过氧化氢的测定方法中,使用α-酮酸。通过本发明的使用α-酮酸的测定方法以及抑制方法,过氧化物的影响得到抑制,能够进行正确的样品中的测定对象成分的测定。

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28-01-2015 дата публикации

Compound For Organic Optoelectronic Device, Organic Light Emitting Diode Including The Same and Display Including The Organic Light Emitting Diode

Номер: KR101486562B1
Принадлежит: 제일모직 주식회사

유기광전자소자용 화합물, 이를 포함하는 유기발광자소자 및 상기 유기발광소자를 포함하는 표시장치에 관한 것으로, 하기 화학식 1로 표시되는 유기광전자소자용 화합물을 제공하여, 우수한 전기화학적 및 열적 안정성으로 수명 특성이 우수하고, 낮은 구동전압에서도 높은 발광효율을 가지는 유기광전자소자를 제조할 수 있다. [화학식 1] 상기 화학식 1의 정의는 본 명세서에 기재된 바와 같다. The present invention relates to a compound for an organic optoelectronic device, an organic light emitting device including the same, and a display device including the organic light emitting device. An organic optoelectronic device having excellent characteristics and high luminous efficiency even at a low driving voltage can be manufactured. [Chemical Formula 1] The definition of the above formula (1) is as described herein.

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10-11-2010 дата публикации

Compounds for organic electronic devices

Номер: EP2248869A2
Принадлежит: Merck Patent GmBH

Heterocyclic compounds (A), are new. Heterocyclic compounds (A) of formula (I) or (II), are new. X : N, P, As, Sb, P=O, As=O or Sb=O; Y 1>O, S, C(R 1>) 2, C=O, C=S, C=NR 1>, C=C(R 1>) 2, Si(R 1>) 2, BR 1>, NR 1>, PR 1>, AsR 1>, SbR 1>, BiR 1>, P(=O)R 1>, As(=O)R 1>, Sb(=O)R 1>, Bi(=O)R 1>, SO, SeO, TeO, SO 2, SeO 2, TeO 2 or a chemical bond; R 1>N, OH, F, Cl, Br, I, CN, NO 2, N(Ar) 2, Si(R 2>) 3, B(OR 2>) 2, 1-40C (preferably 3-40C) alkyl-, alkoxy- or thioalkoxy group (substituted with one or more R 2> residue), where: one or more non-adjacent CH 2 group is substituted by -R 2>C=CR 2>-, -C=C-, Si(R 2>) 2, Ge(R 2>) 2, Sn(R 2>) 2, C=O, C=S, C=Se, C=NR 2>, P(=O)R 2>, S=O, SO 2, NR 2>, -O-, -S- or -CONR 2>, one or more H atoms is substituted by F, Cl, Br, I, CN or NO 2, an aromatic or heteroaromatic ring with 5-40 aromatic ring atoms and an aryloxy- or heteroaryloxy group with 5-24 aromatic ring atoms are substituted by one or more R 2> groups or 2-5 of its combinations, and two or more substituents of R 1> both at the same ring and at different rings together forms a mono- or polycyclic, aliphatic, aromatic or heteroaromatic ring; R : R 1> (where H is unequal to R); R 2>H or aliphatic, aromatic or heteroaromatic 1-20C hydrocarbon, where two or more residues together forms a ring system; Ar : an aromatic or heteroaromatic ring with 5-30 aromatic ring atom (substituted by one or more non-aromatic residues of R 1>); L : chemical bond, 1-40C (preferably 3-40C) alkyl-, alkoxy- or thioalkoxy group (substituted with one or more R 2> residue), P(R 1>) 3 - p, P(=O)(R 1>) 3 - p, Si(R 1>) 4 - p and/or N(Ar) 3 - p, where: one or more adjacent CH 2 group is not substituted by -R 2>C=CR 2>-, -C?=C-, Si(R 2>) 2, Ge(R 2>) 2, Sn(R 2>) 2, C=O, C=S, C=Se, C=NR 2>, P(=O)R 2>, S=O, SO 2, -O-, -S- or -CONR 2>, one or more H atoms is substituted by F, Cl, Br, ...

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22-03-2007 дата публикации

Compounds for organic electronic devices

Номер: WO2007031165A2
Принадлежит: Merck Patent GmBH

The invention relates to the improvement of organic electroluminescent devices, in particular, devices emitting blue light, wherein compounds of formula (1) or formula (2) are used as doping agents in the emitting layer or as hole transport material in a hole transport layer.

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18-05-2007 дата публикации

Compounds for organic electronic devices

Номер: WO2007031165A3

Die vorliegende Erfindung betrifft die Verbesserung organischer Elektrolumineszenzvorrichtungen, insbesondere blau emittierender Vorrichtungen, indem Verbindungen gemäß Formel (1 ) bzw. Formel (2) als Dotanden in der emittierenden Schicht oder als Lochtransportmaterial in einer Lochtransportschicht verwendet werden.

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15-12-2010 дата публикации

Compounds for organic electronic devices

Номер: EP2248869A3
Принадлежит: Merck Patent GmBH

Die vorliegende Erfindung betrifft Verbindungen gemäß Formel (1), welche als funktionelle Materialien in elektronischen Vorrichtungen verwendet werden können. The present invention relates to compounds according to formula (1) which can be used as functional materials in electronic devices.

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22-06-2005 дата публикации

Pyridophenoxazine metal chelate compound

Номер: JP3663528B2
Принадлежит: Ricoh Co Ltd

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30-04-2014 дата публикации

Organic compounds and organic electro luminescence device using the same

Номер: KR101390587B1
Принадлежит: 주식회사 두산

본 발명은 하기 화학식 1로 표시되는 화합물 및 이를 포함하는 유기 전계 발광 소자에 관한 것으로서, 하기 화학식 1로 표시되는 화합물을 하나 이상의 유기층, 바람직하게는 발광층에 포함함으로써, 소자의 발광효율, 구동 전압, 수명 등이 향상될 수 있다: [화학식 1] (상기 화학식 1에서, R 1 ~ R 8 은 각각 상세한 설명에서 정의된 바와 같음). The present invention relates to a compound represented by the following general formula (1) and an organic electroluminescent device comprising the same, wherein the compound represented by the following general formula (1) is contained in at least one organic layer, preferably a light emitting layer, Life and the like can be improved: [Chemical Formula 1] (Wherein R 1 to R 8 are each as defined in the detailed description).

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28-10-2015 дата публикации

Method for detection of a target compound based on a redox-reaction of a phenothiazine dye

Номер: EP2108952B1
Принадлежит: Arkray Inc

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23-06-2021 дата публикации

Electronic devices

Номер: KR102268695B1
Принадлежит: 메르크 파텐트 게엠베하

본 출원은 애노드, 캐소드, 애노드와 캐소드 사이의 하나 이상의 발광층, 호스트로서 모노트리아릴아민을 포함하는 하나 이상의 p-도핑된 층 A, 및 모노트리아릴아민을 포함하는 하나 이상의 층 B 를 포함하는 전자 소자에 관한 것이다. 본 발명은 또한 호스트로서 화학식 (II), (III) 또는 (IV) 의 모노트리아릴아민 및 도펀트로서 전자-받게 화합물을 포함하는 p-도핑된 혼합물 및 전자 소자에서의 상기 혼합물의 용도에 관한 것이다. The present application relates to an electron comprising an anode, a cathode, at least one light emitting layer between the anode and the cathode, at least one p-doped layer A comprising monotriarylamine as host, and at least one layer B comprising monotriarylamine It's about the little ones. The present invention also relates to p-doped mixtures comprising a monotriarylamine of formula (II), (III) or (IV) as host and an electron-accepting compound as dopant and to the use of said mixtures in electronic devices. .

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28-11-2012 дата публикации

Novel Organic Dye And Preparation Method Thereof

Номер: CN102803394A
Автор: 安贤哲, 李钟灿, 裵镐基
Принадлежит: Dongjin Semichem Co Ltd

本发明涉及一种新型染料增感光电转换元件用有机染料及其制造方法,根据本发明的有机染料在染料敏化太阳能电池(dye-sensitized solar cell,DSSC)中作为染料增感光电转换元件而使用,显示比以往的染料更高的摩尔吸光系数、Jsc(短路光电流密度)和光电转换效率,从而可以大大提高太阳能电池的效率。

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01-06-2006 дата публикации

Phenothiazines, -s-oxides, and s,s-dioxides as well as phenoxazines as emitters for oleds

Номер: WO2006056465A1
Принадлежит: BASF AKTIENGESELLSCHAFT

Disclosed is the use of phenoxazine derivatives, phenothiazine derivatives, phenothiazine-S oxide or phenothiazine-S,S dioxide derivatives as emitter substances or hole and exciton blockers in organic light-emitting diodes. The invention further relates to an organic light-emitting diode comprising a light-emitting layer that contains at least one phenoxazine derivative, phenothiazine derivative, phenothiazine-S oxide or phenothiazine-S,S dioxide derivative as an emitter substance, as well as a light-emitting layer which contains or is composed of said phenoxazine derivative, phenothiazine derivative, phenothiazine-S oxide or phenothiazine-S,S dioxide derivative as an emitter substance, a hole and exciton blocking layer that contains or is composed of said phenoxazine derivative, phenothiazine derivative, phenothiazine-S oxide or phenothiazine-S,S dioxide derivative, as well as a device comprising an inventive organic light-emitting diode. The invention finally relates to special phenothiazine-S,S dioxide derivatives, phenothiazine-S oxide derivatives, and phenothiazine derivatives, a method for the production thereof, and the use thereof in organic light-emitting diodes.

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04-10-2011 дата публикации

Phenothiazines, S-oxides, and S,S-dioxides as well as phenoxazines as emitters for OLEDs

Номер: US8029919B2
Принадлежит: BASF SE

The use of phenoxazine, phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivatives as emitter substances in organic light-emitting diodes, an organic light-emitting diode comprising a light-emitting layer, the light-emitting layer comprising at least one phenoxazine, phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivative as an emitter substance, and a light-emitting layer comprising or consisting of the aforementioned phenoxazine, phenothiazine-phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivative as an emitter substance, a hole- and exciton-blocking layer comprising or consisting of the aforementioned phenoxazine derivative, phenothiazine derivative, phenothiazine S-oxide derivative or phenothiazine S,S-dioxide derivative, and a device which comprises an inventive organic light-emitting diode. The present invention further relates to specific phenothiazine S,S-dioxide derivatives, phenothiazine S-oxide derivatives and phenothiazine derivatives and production processes thereof, and to their use in organic light-emitting diodes.

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09-12-2010 дата публикации

Phenothiazines, S-Oxides, And S,S-Dioxides As Well As Phenoxazines As Emitters For Oleds

Номер: US20100308714A1
Принадлежит: BASF SE

The use of phenoxazine, phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivatives as emitter substances in organic light-emitting diodes, an organic light-emitting diode comprising a light-emitting layer, the light-emitting layer comprising at least one phenoxazine, phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivative as an emitter substance, and a light-emitting layer comprising or consisting of the aforementioned phenoxazine, phenothiazine-phenothiazine, phenothiazine S-oxide or phenothiazine S,S-dioxide derivative as an emitter substance, a hole- and exciton-blocking layer comprising or consisting of the aforementioned phenoxazine derivative, phenothiazine derivative, phenothiazine S-oxide derivative or phenothiazine S,S-dioxide derivative, and a device which comprises an inventive organic light-emitting diode. The present invention further relates to specific phenothiazine S,S-dioxide derivatives, phenothiazine S-oxide derivatives and phenothiazine derivatives and production processes thereof, and to their use in organic light-emitting diodes.

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25-06-1975 дата публикации

The method of obtaining oxazine derivatives

Номер: SU474989A3
Принадлежит: Басф Аг (Фирма)

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04-11-2021 дата публикации

Organic light- emitting devices

Номер: KR102321377B1
Принадлежит: 삼성디스플레이 주식회사

유기 발광 소자가 개시된다. An organic light emitting device is disclosed.

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20-10-1979 дата публикации

PROCEDURE FOR THE PRODUCTION OF BASIC BONE DYES

Номер: IT1035459B
Автор:
Принадлежит: Ciba Geigy AG

Подробнее
07-05-1981 дата публикации

Process for the preparation of oxazine dyes

Номер: DE2210074C3
Принадлежит: BASF SE

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06-05-2010 дата публикации

Method for detecting phenothiazine-derivative color and color-developer reagent used therein

Номер: US20100112622A1
Принадлежит: Arkray Inc

The present invention provides a phenothiazine-derivative color-measuring method that can detect a phenothiazine-derivative color even at a wavelength longer than the wavelength that exhibits maximum absorption. A phenothiazine-derivative color is detected, by adding a 5-hydroxy-1-(4-sulfophenyl)-4-(4-sulfophenylazo)pyrazole-3-carboxylic acid salt, 6-hydroxy-5-(4-sulfophenylazo)-2-naphthalenesulfonic acid salt, 3-hydroxy-4-(4-sulfonaphthylazo)-2,7-naphthalenedisulfonic acid salt, 7-hydroxy-8-(4-sulfonaphthylazo)-1,3-naphthalenedisulfonic acid salt, 3′,6′-dihydroxy-2′,4′,5′,7′-tetraiodospiro[isobenzofuran-1(3H),9′-(9H)xanthene]-3-one salt, 3′,6′-dihydroxy-2′,4′,5′,7′-tetrabromo-4,5,6,7,-tetrachlorospiro[isobenzofuran-1(3H),9′-[9H]xanthene]-3-one salt, 4,5,6,7-tetrachloro-3′,6′-dihydroxy-2′,4′,5′,7′-tetraiodospiro[isobenzofuran-1(3H),9′-[9H]xanthene]-3-one salt or flavonoid-based color to the reaction system containing a phenothiazine-derivative color, and then measuring the light absorbance at a wavelength of 610 to 730 nm.

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18-07-1983 дата публикации

Patent FR2480767B1

Номер: FR2480767B1
Автор:

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23-10-1981 дата публикации

PROCESS FOR THE PREPARATION OF BASIC OXAZINIC DYES

Номер: FR2480767A1
Автор: Gerard Belfort

L'INVENTION CONCERNE UN PROCEDE DE PREPARATION DE COLORANTS DE FORMULE: (CF DESSIN DANS BOPI) DANS LAQUELLE R H, ALKYL, ALCENYL OU ARALKYL, R ALKYL, ALCENYL, CYCLOALKYL, ARYL OU ARALKYL, R H, ALKYL OU ALCOXY, R H, ALKYL, ARYL OU ARALKYL, R H OU ALKYL, R H, ALKYL OU ALCOXY, R H OU ALKYL OU FORME AVEC R UN NOYAU BENZENIQUE CONDENSE ET X REPRESENTE UN ANION, QUI CONSISTE A FAIRE REAGIR UN COMPOSE NITROSO II AVEC UN AMINOPHENOL III OU UN COMPOSE NITROSO IV AVEC UN COMPOSE V: (CF DESSIN DANS BOPI) DANS LESQUELLES R A R ONT LES MEMES SIGNIFICATIONS QUE CI-DESSUS, R, R ET R REPRESENTENT CHACUN H OU ALKYL, R EST UN RADICAL ALKYLE EVENTUELLEMENT SUBSTITUE ET R EST UN RADICAL ALCOXY OU UN GROUPE AMINO EVENTUELLEMENT SUBSTITUE. THE INVENTION CONCERNS A PROCESS FOR THE PREPARATION OF COLORANTS OF FORMULA: (CF DRAWING IN BOPI) IN WHICH RH, ALKYL, ALCENYL OR ARALKYL, R ALKYL, ALCENYL, CYCLOALKYL, ARYL OR ARALKYL, RH, ALKYL, RH, ALKYL OR ALKYL, RH, ALKYL, RH, ALKYL OR ALKYL ARYL OR ARALKYL, RH OR ALKYL, RH, ALKYL OR ALCOXY, RH OR ALKYL OR FORMED WITH R A BENZENIC CORE CONDENSED AND X REPRESENTS AN ANION, WHICH CONSISTS OF REACTING A NITROSO II COMPOUND WITH AN AMINOPHENOL III OR AN IV COMPOUND WITH NITROSO A V COMPOUND: (CF DRAWING IN BOPI) IN WHICH RAR HAVE THE SAME MEANINGS AS ABOVE, R, R AND R EACH H OR ALKYL, R IS A RADICAL ALKYL POSSIBLE SUBSTITUTE AND R IS A RADICAL ALCOXY OR AN AMINO GROUP POSSIBLE SUBSTITUTE.

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03-02-1978 дата публикации

PROCESS FOR THE PRODUCTION OF OXAZENIC COLORANTS

Номер: FR2357603A1
Автор: [UNK]
Принадлежит: Bayer AG

L'invention décrit la production de colorants oxazéniques basiques. On effectue la nitrosation de 3-(bêta-hydroxyalcoxy)-arylamines en présence d'un acide puis l'on condense avec des phénols. Ces colorants peuvent servir à la teinture et à l'impression de textiles, notamment du coton. The invention describes the production of basic oxazene dyes. The nitrosation of 3- (beta-hydroxyalkoxy) -arylamines is carried out in the presence of an acid and then condensed with phenols. These dyes can be used for dyeing and printing textiles, especially cotton.

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27-07-1953 дата публикации

Improvements in the preparation of 9-aminobenzophenoxazines

Номер: FR1034592A
Автор:
Принадлежит: American Cyanamid Co

Подробнее
09-07-1976 дата публикации

Basic oxazine dyes prepn. - from nitroso and amino cpds., for dyeing and printing polyacrylonitrile, leather, polyamides etc. (BE100676)

Номер: FR2294209A1
Автор: [UNK]
Принадлежит: Hoechst AG

Basic oxazine dyes of formula (I): (where R and R5 are H, lower alkyl or alkoxy; R1-R3 are H, lower alkyl opt. substd. by OH, CN, carboxylic acid amide or ester; R4 is H, lower alkyl, phenyl opt. substd. by halogen, lower alkyl and/or alkoxy, or benzyl; or NR3R4 forms a heterocycle; X - is an anion) are prepd. by condensing a nitroso cpd. of formula (II): with an amino cpd. of formula (III): (where Z is H, OH, lower alkoxy, prim. sec. or tert. amino, or aminosulphonic acid gp.) in a lower aliphatic alcohol in acid medium. In this process, the soln. or suspension of the nitros cpd. obtd. by nitrosation of a m-amino-phenol in a lower aliphatic alcohol is heated to 50-80 degrees C and then m-aminophenol, m-aminophenol ehter, m-phenylene diamine or its mono- N-sulphonic acid added, and the condensn. effected. Dyes are used for deying/printing tanned cellulose fibres, silk, wool, acetate, polyamides, acid-modified polyamides and polyesters and esp. fibres contg. polyacrylonitrile or polyvinylidene cyanide pale greenish blue shades with good light- and wet-fastness. The dyes are obtd. in improved quality and yield.

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19-07-1968 дата публикации

Process for preparing dyes belonging to the oxazine series

Номер: FR1533638A
Автор:
Принадлежит: Farbwerke Hoechst AG, Hoechst AG

Подробнее
11-06-1976 дата публикации

Patent FR2171260B1

Номер: FR2171260B1
Автор: [UNK]
Принадлежит: BASF SE

Подробнее
11-06-1976 дата публикации

Patent FR2174235B1

Номер: FR2174235B1
Автор: [UNK]
Принадлежит: BASF SE

Подробнее
28-04-1978 дата публикации

DYES BASED ON PHENOXAZINE DERIVATIVES FOR DYING TEXTILE SUBSTRATES

Номер: FR2366402A1
Принадлежит: SANDOZ AG

L'invention a pour objet l'application de dérivés de la phénoxazine comme colorants pour la teinture, la coloration dans la masse ou l'impression de substrats textiles. Les colorants de l'invention répondent à la formule : The subject of the invention is the application of phenoxazine derivatives as dyes for the dyeing, bulk coloring or printing of textile substrates. The dyes of the invention correspond to the formula:

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14-01-1994 дата публикации

Process for the preparation of oxazine-type dyes

Номер: FR2693468A1
Принадлежит: Ciba Geigy AG

On décrit un procédé de préparation de colorants de type oxazine, basiques et exempts de zinc, de formule (CF DESSIN DANS BOPI) qui est caractérisé en ce que l'on effectue la nitrosation d'un composé de formule (CF DESSIN DANS BOPI) dans un milieu contenant un solvant polaire, aprotique et miscible à l'eau, de préférence du N,N-diméthylformamide, de l'acide nitrique (HNO3 ) et éventuellement de l'eau et/ou un alcanol en C1 - 4 , b) on condense le composé nitroso obtenu, sans l'isoler, avec un composé de formule (CF DESSIN DANS BOPI) et c) le cas échéant, on chasse par distillation l'eau et l'alcanol en C1 - 4 , jusqu'à ce que le sel colorant précipite. A process for the preparation of oxazine-type dyes, basic and free of zinc, of formula (CF DRAWING IN BOPI) is described which is characterized in that the nitrosation of a compound of formula (CF DRAWING IN BOPI) is carried out in a medium containing a polar solvent, aprotic and miscible with water, preferably N, N-dimethylformamide, nitric acid (HNO3) and optionally water and / or a C1-4 alkanol, b ) the nitroso compound obtained is condensed, without isolating it, with a compound of formula (CF DRAWING IN BOPI) and c) where appropriate, the water and the C1 - 4 alkanol are distilled off, until what the coloring salt precipitates.

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15-06-1959 дата публикации

Process for dyeing articles of polyester

Номер: FR1181377A
Автор:
Принадлежит: Badische Anilin and Sodafabrik AG, BASF SE

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01-09-1955 дата публикации

Process for dyeing and printing polyacrylonitrile fibers, and dyeing and printing thus obtained

Номер: FR1099280A
Автор:
Принадлежит: Ciba Geigy AG

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18-08-1972 дата публикации

Patent FR2121198A5

Номер: FR2121198A5
Автор: [UNK]
Принадлежит: Farbwerke Hoechst AG, Hoechst AG

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25-07-1907 дата публикации

Process for the preparation of a gallocyanin leukobase

Номер: FR375864A
Автор:
Принадлежит: Individual

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27-08-1907 дата публикации

Process for the preparation of a leucogallocyanin derived from pyrogallol

Номер: FR377024A
Автор:
Принадлежит: L Durand Huguenin & Cie

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11-04-2018 дата публикации

Electronic devices

Номер: TWI620810B
Принадлежит: 馬克專利公司

本申請案係關於一種電子裝置,其包含陽極、陰極、該陽極與該陰極間之至少一發射層、包含單三芳基胺作為主體之至少一p-摻雜層A及包含單三芳基胺之至少一層B。此外,本發明係關於一種包含式(II)、(III)或(IV)之單三芳基胺作為主體及包含電子-受體化合物作為摻雜劑之p-摻雜混合物,及該混合物於電子裝置中之用途。

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29-09-2020 дата публикации

Oxidation color developable compound and oxidation color development reagent

Номер: US10787571B2
Принадлежит: Dojindo Laboratory and Co Ltd

The present invention pertains to: an oxidation color developable compound that is represented by general formula (1), that has excellent solubility in water, and that is less affected by a substance coexisting in a sample; and an oxidation color development reagent using the oxidation color developable compound. In general formula (I), R 1 , R 2 , R 3 , and R 4 each represent a straight-chain or branched alkyl group having 1-6 carbon atoms, X represents a hydrophilic functional group, and L represents —(CH 2 ) j — (j represents an integer of 2-10), —(CH 2 CH 2 O) k — (k represents an integer of 1-10), or —(CH 2 ) m —Z—(CH 2 ) n — (m and n each independently represent an integer of 1-10, and Z represents —N + (CH 3 ) 2 —, —CONH—, —NHCO—, —COO—, —OCO—, —NHCOO—, —OCONH—, —NHCONH—, and —(CH 2 NHCO) q —).

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31-10-1978 дата публикации

Basic oxazine dyes prepn.

Номер: CH606279A5
Принадлежит: SANDOZ AG

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22-01-2016 дата публикации

Dye sensitized sola cell and dye compond used therefin

Номер: KR101587829B1
Автор: 강진규, 김효정, 남정은
Принадлежит: 재단법인대구경북과학기술원

본 발명은 유기염료 화합물 및 이를 포함하는 염료감응 태양전지에 관한 것으로서, 보다 상세하게는 광전 변환 효율이 향상된 유기염료 화합물 및 이를 포함하는 염료감응 태양전지에 관한 것이다.

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19-03-1919 дата публикации

Process for the preparation of condensation products of gallocyanines with amines

Номер: FR489868A
Автор:

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11-06-2021 дата публикации

Near-infrared fluorescent probe capable of detecting content of GSTs (glutathione S-terminal transferase) as well as synthetic method and application thereof

Номер: CN112939886A
Принадлежит: SHANXI UNIVERSITY

本发明提供了一种可检测GSTs含量的近红外荧光探针及其合成方法和应用。所述探针的名称为4‑(2,4‑二硝基苯氧基)苄基3,7‑双(二乙氨基)‑10H‑苯恶嗪‑10‑羧酸盐(4‑(2,4‑dinitrophenoxy)benzyl 3,7‑bis(diethylamino)‑10H‑phenoxazine‑10‑carboxylate),或4‑(2,4‑二硝基苯氧基)苄基3,7‑双(二甲氨基)‑10H‑吩噻嗪‑10‑羧酸盐(4‑(2,4‑dinitrophenoxy)benzyl l 3,7‑bis((diethylamino)‑10H‑phenoxazine‑10‑carboxylate)。本发明还提供了一种检测体内GSTs含量的方法,即将所述探针在磷酸缓冲溶液pH=7:乙醇/9:1(v/v)体系中,通过荧光分光光度计对GSTs的含量进行定量检测。该检测方法灵敏度高,方法简便。

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04-08-2011 дата публикации

Novel organic electroluminescent compounds and organic electroluminescent device using the same

Номер: WO2011093609A1

Provided are organic electroluminescent compounds of a fused pentacyclic structure of general formula I, and an organic electroluminescent device using said compounds. Since the organic electroluminescent compounds exhibit good luminous efficiency and lifespan, they may be used to manufacture OLED devices which have a superior operational lifetime and also have low power consumption due to the improved power efficiency of the compounds.

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11-11-1986 дата публикации

Phenoxazine and phenothiazine dyes and leuco forms thereof

Номер: US4622395A
Принадлежит: Minnesota Mining and Manufacturing Co

Novel phenoxazine and phenothiazine dyes have the formula ##STR1## wherein X can be --S-- or --O--; each R can be the same or different and is independently selected from (1) hydrogen, (2) an unsubstituted aryl or alkyl group or these groups substituted by up to four groups selected from alkyl, alkoxy, cyano, hydroxy, halogen, nitro, mercapto, alkylsulfonyl, arylsulfonyl, and Z, where Z is as defined below, wherein all alkyl and alkoxy groups have 1 to 20 carbon atoms; and (3) Z, wherein Z can be ##STR2## wherein each Q can be the same or different and is independently selected from (1) hydrogen, (2) an unsubstituted aryl or alkyl group or these groups substituted by up to four groups selected from alkyl, alkoxy, cyano, hydroxy, halogen, nitro, mercapto, alkylsulfonyl, arylsulfonyl, and Z, where Z is as defined above, wherein all alkyl and alkoxy groups have 1 to 20 carbon atoms; and R' is the same or different and is independently selected from hydrogen, halogen, alkyl or alkoxy of 1 to 6 carbon atoms or these groups substituted by up to 3 halogen atoms; and A is an anion; with the proviso that R and L can have up to a total of 5 carbonyl and sulfonyl groups, and with the proviso that the average value of a Taft Constant and of a Hammett Constant for the two R groups on at least one 3- or 7-position nitrogen atom is greater than 1.0 for a Taft Constant and greater than +0.1 for a Hammett Constant.

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14-03-1974 дата публикации

Process for the preparation of oxazine dyes

Номер: DE1569603C3
Принадлежит: Farbwerke Hoechst AG

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05-10-1978 дата публикации

METHOD FOR PRODUCING M-AMINOPHENOLS AND THEIR USE

Номер: DE2714255A1
Принадлежит: Hoechst AG

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08-06-1974 дата публикации

Patent JPS4959134A

Номер: JPS4959134A
Автор:
Принадлежит:

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26-11-2013 дата публикации

Novel phenothiazine derivates, preparation method thereof and organic solar cell having them

Номер: KR101309208B1
Принадлежит: 한국화학연구원

본 발명은 신규한 페노티아진계 유도체에 관한 것으로, 더욱 구체적으로는 상기 유도체를 염료감응 태양전지의 염료로 사용하여 광전변환효율이 현저히 향상될 뿐만 아니라, 페노티아진기에 알킬기를 도입함으로써 염료 분자간의 응집이 방지되고 열적, 광적 안정성이 향상되므로, 준고상 전해질을 사용하는 염료감응 태양전지의 염료 및 고분자/단분자 혼합형 태양전지의 단분자로 유용하게 사용될 수 있다. The present invention relates to a novel phenothiazine derivative, and more particularly, the use of the derivative as a dye of a dye-sensitized solar cell not only significantly improves the photoelectric conversion efficiency, but also introduces an alkyl group to the phenothiazine to induce Since agglomeration is prevented and thermal and optical stability are improved, it can be usefully used as a single molecule of a dye and a polymer / molecule mixed solar cell of a dye-sensitized solar cell using a semi-solid electrolyte.

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02-10-1970 дата публикации

Cytologic dye for staining microscope sam- - ples

Номер: FR2027498A1
Автор: [UNK]
Принадлежит: DOUSSET ANDRE

Cytologic dye comprises an alcoholic soln. pH 6.5 contng. 4-6 g./l. of a mixture of 1 pbw. casein, per 2-3 pbw. methylene blue, i.e. a "Wright dye" and 75-125 ml./l. glycerine. The alcoholic soln. is pref. methanolic contng. a small amt. phenol, pref. 0.1%. Prepd. by heating the glycerine to 40 degrees C., adding the Wright dye and mixing, slowly adding phenolated methanol then absolute methanol, and heating at 40 degrees C. for three days. The mixture is then filtered and the filtrate pH adjusted to 6.5. The dyes are used for staining dried cytologic wafer specimens by covering them for three mins. with 15-25 drops of dye and 15-25 drops distilled water, mixing, washing with water and then drying.

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10-09-1999 дата публикации

Photodetector, and the use thereof

Номер: CA2322458A1
Принадлежит: Individual

The invention relates to a device for detecting electromagnetic radiation, characterised in that it has i) a photoactive layer consisting of a semiconductor with a band gap of over 2.5 eV, ii) a dye which is applied to the semiconductor and iii) a charge transfer layer containing a hole conductor material, said hole conductor material being preferably solid and amorphous.

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30-03-1966 дата публикации

Chromone compounds

Номер: GB1024646A
Принадлежит: BENGER LAB Ltd

The invention comprises chromone derivatives of the general formula <FORM:1024646/C2/1> and salts and esters thereof in which R1 is a hydrogen atom or a lower alkyl group or together with the carbon atom in the ring forms a carbonyl group and a process for the preparation thereof by condensing a compound of the formula <FORM:1024646/C2/2> with diethyl oxalate and subsequently cyclising the resultant diketone by heating with a mixture of glacial acetic acid and hydrochloric acid. The starting carboxyl compound may be prepared by reducing 5-nitroresacetophenone to 5-aminoresacetophenone, chloracetylating the amino group and subsequently heating with potassium acetate or by reacting 5-benzoyloxy-2-nitrophenol with chloracetone to yield 5-benzoyloxy - 2 - nitrophenoxy - acetone followed by hydrogenation to yield 7-benzoyloxy-3,6-dihydro - 3 - methyl - 2 - H - 1,4 - benzoxazone and acetylation. Pharmaceutical compositions having activity as inhibitors of the antigen-antibody reaction and containing the above compounds are administered orally in tablets, in solutions for injection, or topically in creams, lotions, pastes or in an aerosol.

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04-02-1977 дата публикации

PROCESS FOR PREPARING BASIC OXAZINIC DYES

Номер: FR2317336A1
Автор: [UNK]
Принадлежит: Ciba Geigy AG

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19-03-1998 дата публикации

Process for the preparation of polymers in the presence of triazolyl radicals

Номер: DE19636996A1

The invention concerns a process for preparing polymers, characterized in that polymerization is carried out in the presence of radicals of general formula (I), in which Q means NR<2> or S and T means CR<4>R<5> or S, and R<1>, R<2>, R<3> and R<4> may be the same or different from one another and independently of one another mean hydrogen, C1-C20 alkyl or C6-C18 aryl.

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12-01-2010 дата публикации

Photosensitizer dye

Номер: US7645879B2
Принадлежит: National Central University

A photosensitizer dye is provided. The photosensitizer dye is a Ru complex as formula (1):

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20-01-1981 дата публикации

Basic indoline dyestuffs

Номер: US4246404A
Автор: Berthold Gertisser
Принадлежит: SANDOZ AG

Basic dyestuffs free of sulphonic acid groups contain an indoline group the 2-position of which is connected through a vinylene group to the N-atom of a 2,3-dihydro-4H-1,4-benzoxazine group. The dyestuffs are useful for the dyeing of leather, paper and plastics and, particularly, polyacrylonitrile or acid-modified polyester fibres.

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15-06-1977 дата публикации

METHOD FOR PREPARING OXAZINE BASIC COLORING AGENTS.

Номер: NL153588B
Автор:
Принадлежит: Hoechst AG

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22-09-2011 дата публикации

Arsenical fluorescent agents and assays

Номер: CA2788292A1
Принадлежит: SRI International Inc

The invention provides methods and compositions for labeling dithiol-containing analytes.

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07-04-2021 дата публикации

Method for measuring component to be measured in specimen

Номер: EP2843054B1

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15-09-1981 дата публикации

Cationic oxazine dyes

Номер: US4289880A
Автор: Peter Moser
Принадлежит: Ciba Geigy Corp

There are described new blue cationic oxazine dyes of the formula ##STR1## in which R 1 , R 2 , R 3 and R 4 independently of one another are each C 1-4 -alkyl, with R 1 and R 2 together with the nitrogen atom also being able to form a heterocyclic ring, and X.sup.⊖ is an anion; these dyes are distinguished in particular by an excellent migration capacity on polyacrylonitrile fibres.

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27-11-1979 дата публикации

PROCESS FOR THE PREPARATION OF ORGANIC COMPOUNDS AND THEIR USE

Номер: BR7902891A
Автор: B Gertisser
Принадлежит: SANDOZ AG

Подробнее
24-03-1982 дата публикации

Light-sensitive dyestuffs

Номер: GB2083488A
Автор:

Compositions for use in photogalvanic cells comprising as light-sensitive compounds heterocyclic compounds according to the general formula <IMAGE> wherein n, X, R<1>, R<2>, Y<1>, Y<2>, Y<3>, Z<1>, Z<2>, Z<3>, Z<4>, B and m having defined meanings. The compounds of this general formula (I) with the exception of 3,7-bis(4- methyl- 1 -piperazinyl)phenothiazonium bromide are claimed per se.

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01-04-2011 дата публикации

Novel organic dye and preparation thereof

Номер: TW201112469A
Принадлежит: Dongjin Semichem Co Ltd

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09-04-1931 дата публикации

Manufacture of dyestuffs

Номер: GB346243A
Автор:
Принадлежит: Durand and Huguenin AG

Gallocyanines; printing.-Simple gallocyanines derived from meta-substituted alkylaniline, and having the general constitution defined in the parent Specification, are converted into derivatives, which still retain the meta-substituent, by condensation with an aromatic hydroxy compound. The latter may contain sulphonic groups, or the products may be sulphonated, either in the lenco form or in the oxidized form, to render them soluble in water. The products, like those of the parent Specification, show greater resistance to reducing agents as compared with the corresponding dyes unsubstituted in the meta-position (see Specifications 24802/93, 15064/94, 16301/95, [all in Class 2, Acids and salts, Organic &c.], and 6272/09, [Class 2 (iii), Dyes &c.]), and are suitable for use in discharge printing. In examples, (1) the simple gallocyanines from nitrosodimethyl- or -diethyl-m-toluidine and gallomide are condensed with resorcin or with another aromatic hydroxy compound, such as b -resorcylic acid, pyrogallol or gallic acid, in the presence of hydrochloric acid; the products may be sulphonated by treating their dry-leaved compounds with sulphuric acid, and (2) the gallocyanine from nitrosodimethyl-m-toluidine and gallic acid is condensed with 2-naphthol-6-sulphonic acid in the presence of caustic soda or of an acid; other naphthol-sulphonic acids or aromatic oxycompounds may be used.

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15-02-1980 дата публикации

CATIONIC OXAZINIC DYES, PROCESS FOR THEIR PREPARATION AND THEIR USE

Номер: FR2431520A1
Автор: Peter Moser
Принадлежит: Ciba Geigy AG

Colorants oxaziniques cationiques, leur procédé de préparation et leur utilisation. La présente invention décrit de nouveaux colorants oxaziniques cationiques bleus ayant la formule : Cationic oxazine dyes, their preparation process and use. The present invention describes novel blue cationic oxazine dyes having the formula:

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23-10-2002 дата публикации

Chromophoric compounds and their preparation process

Номер: EP0943661B1
Принадлежит: SIEMENS AG

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11-12-2020 дата публикации

Organic electroluminescent element

Номер: KR102190183B1

유기 일렉트로 루미네선스 소자는, 양극과, 음극과, 발광층을 포함하고, 상기 발광층은, 제 1 화합물 및 제 2 화합물을 함유하고, 상기 제 1 화합물 및 상기 제 2 화합물은, 열 활성 지연 형광 발광성의 화합물인 것을 특징으로 한다. The organic electroluminescence device includes an anode, a cathode, and an emission layer, the emission layer contains a first compound and a second compound, and the first compound and the second compound are thermally activated delayed fluorescence emission It is characterized in that it is a compound of.

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05-04-2013 дата публикации

Novel organic dye incorporating a benzothiadiazole chromophore and preparation thereof

Номер: KR101250403B1
Автор: 고재중, 김점종, 이종찬

본 발명은 벤조티아다이아졸 발색부-함유 신규 유기염료 및 이의 제조방법에 관한 것으로, 본 발명의 염료 화합물은 종래의 염료보다 높은 광전지 성능 및 우수한 안정성을 가져 염료감응태양전지(dye-sensitized solar cell, DSSC)에 사용되어 전지의 효율을 크게 향상시킬 수 있다. The present invention relates to a benzothiadiazole chromophore-containing novel organic dye and a method for preparing the same. The dye compound of the present invention has higher photovoltaic performance and superior stability than conventional dyes, and thus dye-sensitized solar cells. , DSSC) can greatly improve the efficiency of the battery. 태양전지, 염료감응, 염료, 광전변환소자, 벤조티아다이아졸 Solar cell, dye-sensitized, dye, photoelectric conversion element, benzothiadiazole

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25-06-1980 дата публикации

Process for the preparation of oxazine dyestuffs

Номер: GB1570109A
Автор:
Принадлежит: Bayer AG

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11-12-2018 дата публикации

swab for mouth sampling and uses

Номер: BR112018013189A2
Принадлежит: Procter & Gamble

a presente invenção refere-se a um zaragatoa para amostragem bucal (1) para avaliar visualmente a eficácia do tratamento de um produto para tratamento bucal em reduzir a quantidade de bactérias em uma cavidade bucal e método de uso da mesma. The present invention relates to a buccal sampling swab (1) for visually assessing the effectiveness of treating a buccal treatment product in reducing the amount of bacteria in a buccal cavity and method of use thereof.

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24-09-1974 дата публикации

Basic oxazine dyestuffs and process for their preparation

Номер: CA955256A
Принадлежит: Farbwerke Hoechst AG

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28-05-2008 дата публикации

Compounds for organic electronic devices

Номер: EP1924670A2
Принадлежит: Merck Patent GmBH

The invention relates to the improvement of organic electroluminescent devices, in particular, devices emitting blue light, wherein compounds of formula (1) or formula (2) are used as doping agents in the emitting layer or as hole transport material in a hole transport layer.

Подробнее
16-07-1994 дата публикации

DIRECT DYES.

Номер: ES2052852T3
Принадлежит: Bayer AG

EL INVENTO TRATA DE UN COLORANTE DIRECTO DE FORMULA (I) A BASE DE TRIFENODIOXAZINA PARA COLOREAR MATERAIELES NATURALES Y SINTETICOS CONTENIENDO GRUPOS OH Y NH DE AZUL CLARO, PRODUCIENDO ESTRUCTURAS CON BUENAS PROPIEDADES DE LUZ Y HUMEDAD. THE INVENTION IS ABOUT A DIRECT DYE OF FORMULA (I) BASED ON TRIPHENODIOXAZINE TO COLOR NATURAL AND SYNTHETIC MATERAIELS CONTAINING OH AND NH GROUPS OF LIGHT BLUE, PRODUCING STRUCTURES WITH GOOD PROPERTIES OF LIGHT AND MOISTURE.

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