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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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Применить Всего найдено 29. Отображено 29.
15-02-2012 дата публикации

POLYMERE AND POLYMER COMPOSITIONS

Номер: AT0000542842T
Принадлежит:

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21-10-2012 дата публикации

IMPROVEMENTS IN POLYMERS

Номер: CA0002774631A1
Принадлежит: Infineum International Ltd

A sulphur-free polymer comprising structural units of formula (I) and structural units of formula (II): (see formula I) (see formula II) wherein R1 represents a C8 to C22 alkyl group, preferably a C12 to C16 alkyl group; wherein R2 is hydrogen or methyl; wherein R3 represents -R5(OR6)n OR7 ; wherein R5 and R6 may be the same or different and independently represent a linear or branched C1 to C8 alkylene group; wherein n is an integer from 1 to 20; wherein R7 represents a C1 to C4 alkyl group; wherein R4 is hydrogen or methyl; and wherein the molar ratio of structural units (I): structural units (II) in the polymer is in the range from 100:1 to 2:1. The polymers improve the low-temperature properties of fuel oils from petroleum sources, those from vegetable or animal sources, and mixtures of these fuel oils.

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05-12-2001 дата публикации

Liquid crystalline optionally laterally fluorinated terphenyl with chiral 3,4-di[(un)saturated-alkoxy]butoxy or 1,4-di[(un)saturated-alkoxy]but-2-oxy terminus

Номер: GB0002362882A
Принадлежит:

The invention relates to terphenyl compounds having the general formula [1]:- where each of R1 and R2 is the same or different and is selected from the group consisting of:-alkyl, alkyloxy, alkylthio, alkenyl, alkenyloxy, alkenylthio, alkynyl, alkynyloxy, alkynylthio, where * indicates an asymmetric carbon atom,
provided that at least one of R1 and R2 is and where each of R3 and R4 is the same or different and is an alkyl, alkenyl or alkynyl group; and Z is independently selected from hydrogen and fluorine at each of the four lateral terphenyl carbons in each ring. The compounds are suitable for use in liquid crystal compositions.

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02-04-2003 дата публикации

BENZOFURAN COMPOUNDS THEIR PREPARATION AND THEIR USE IN ELECTROLUMINESCENT AND PHOTOVOLTAIC DEVICES

Номер: GB0002380191A
Принадлежит:

A method of preparing a branched benzofuran compound comprising a core moiety which contains at least one aromatic ring and which has at least three substituted or unsubstituted beuzofuran groups covalently linked thereto comprises the steps of

  • (i) forming an intermediate ethynylene compound in which at least three benzene rings are each linked to the core moiety via an ethynylene bond, and where each benzene ring is substituted at the ortho position (relative to the position of the ethynylene bond) by a blocked carbonyloxy group,
  • (ii) deblocking the carbonyloxy groups, and
  • (iii) effecting ring closure by reaction between the deblocked carbonyloxy groups and the adjacent ethynylene bonds to form the furan rings of the beuzofuran groups, whereby to produce the branched benzofuran compound. The invention also comprises compounds of Formulae where each of R 1 to R 8 is independently selected from H, an aliphatic group ...

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  • 22-12-1993 дата публикации

    1-Methyl-2-oxaalkoxy derivatives in thermochromic liquid crystalline compositions and surface thermography

    Номер: GB0002267910A
    Принадлежит: Merck Patent GmBH

    The invention relates to the use of 1-methyl-2-oxaalkoxy derivatives of the formula I <IMAGE> [wherein R<1>, R<2> <IMAGE> Z, X1, Q, o and m have the meaning given in claim 1] as components of thermochromic liquid crystalline compositions and the use of a thin film of such compounds (or a liquid crystalline phase containing such compounds) in a method of surface thermography. Subclasses of compounds of formula I are claimed per se (see claims 2-4).

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    26-08-2004 дата публикации

    Terphenylverbindungen

    Номер: DE0060104363D1
    Принадлежит: SHARP KK, SHARP K.K., OSAKA

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    18-12-2008 дата публикации

    ADDITIVES AND LUBRICATING OIL COMPOSITIONS CONTAINING SAME

    Номер: CA0002690200A1
    Принадлежит:

    Para-alkylated substituted diphenylamines are made by catalytically alkylating diphenylamine with a branched-chain alkene, such as propene, oligomer mixture in which the oligomer present in the greatest percentage has 15-24 carbon atoms. The alkylated diphenylamines are useful crankcase lubricant additives such as for reducing piston deposits and engine sludge.

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    11-10-2016 дата публикации

    IMPROVEMENTS IN POLYMERS

    Номер: CA0002726106C

    Ter-polymers are higher polymers comprising as structural units, units of formula I, units of formula II and units of either formula IIIa or formula IIIb: (see formula I) (see formula II) (see formula IIIa) (see formula IIIb) and optionally and optionally, structural units of formula VII: (see formula VII) The polymers improve the low-temperature properties of fuel oils from petroleum sources and especially from vegetable or animal sources.

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    21-06-2011 дата публикации

    IMPROVEMENTS IN POLYMERS

    Номер: CA0002726106A1
    Принадлежит:

    Ter-polymers are higher polymers comprising as structural units, units of formula I, units of formula II and units of either formula IIIa or formula IIIb: (see formula I) (see formula II) (see formula IIIa) (see formula IIIb) and optionally and optionally, structural units of formula VII: (see formula VII) The polymers improve the low-temperature properties of fuel oils from petroleum sources and especially from vegetable or animal sources.

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    31-07-2018 дата публикации

    IMPROVEMENTS IN POLYMERS

    Номер: CA0002774631C

    A sulphur-free polymer comprising structural units of formula (I) and structural units of formula (II): (see formula I) (see formula II) wherein R1 represents a C8 to C22 alkyl group, preferably a C12 to C16 alkyl group; wherein R2 is hydrogen or methyl; wherein R3 represents -R5(OR6)n OR7 ; wherein R5 and R6 may be the same or different and independently represent a linear or branched C1 to C8 alkylene group; wherein n is an integer from 1 to 20; wherein R7 represents a C1 to C4 alkyl group; wherein R4 is hydrogen or methyl; and wherein the molar ratio of structural units (I): structural units (II) in the polymer is in the range from 100:1 to 2:1. The polymers improve the low-temperature properties of fuel oils from petroleum sources, those from vegetable or animal sources, and mixtures of these fuel oils.

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    30-09-2014 дата публикации

    ADDITIVES AND LUBRICATING OIL COMPOSITIONS CONTAINING SAME

    Номер: CA0002690200C

    Para-alkylated substituted diphenylamines are made by catalytically alkylating diphenylamine with a branched-chain alkene, such as propene, oligomer mixture in which the oligomer present in the greatest percentage has 15-24 carbon atoms. The alkylated diphenylamines are useful crankcase lubricant additives such as for reducing piston deposits and engine sludge.

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    07-04-2003 дата публикации

    BENZOFURAN COMPOUND

    Номер: KR20030027862A
    Принадлежит:

    PURPOSE: Provided is a branched benzofuran compound which is suitable for charge transport and emission inorganic electroluminescent devices and organic lasers. The compounds also have potential use in photovoltaic devices and organic thin film transistors. CONSTITUTION: A method for preparing a branched benzofuran compound comprising a core moiety which contains at least one aromatic ring and which has at least three substituted or unsubstituted benzofuran groups covalently linked thereto, is characterized by comprising the steps of (i) forming an intermediate ethynylene compound in which at least three benzene rings are each linked to the core moiety via an ethynylene bond, and where each benzene ring is substituted at the ortho position (relative to the position of the ethynylene bond) by a blocked carbonyloxy group, (ii) deblocking the carbonyloxy groups, and (iii) effecting ring closure by reaction between the deblocked carbonyloxy groups and the adjacent ethynylene bonds to form the ...

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    29-06-2011 дата публикации

    POLYMER EFFECTIVE IN THE IMPROVEMENT OF LOW-TEMPERATURE CHARACTERISTIC OF FUEL OIL, A FUEL OIL COMPOSITION CONTAINING THE POLYMER, AND USE OF THE POLYMER

    Номер: KR1020110073297A
    Принадлежит:

    PURPOSE: A polymer is provided to improve low temperature characteristics of fuel oil from oil resources, especially vegetable or animal resources. CONSTITUTION: A polymer comprises a structure unit of chemical formula (I), a structure unit of chemical formula (II), a structure unit of chemical formula (IIIa) or (IIIb), and arbitrarily a structure unit of chemical formula (VII). The fuel oil composition comprises the polymer. The fuel oil includes fatty acid alkyl ester prepared from oil induced from animal or vegetable materials. The additive concentrate comprises a polymer and a miscible solvent or carrier. COPYRIGHT KIPO 2011 ...

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    25-08-2005 дата публикации

    Terphenylverbindungen

    Номер: DE0060104363T2
    Принадлежит: SHARP KK, SHARP K.K., OSAKA

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    12-12-2001 дата публикации

    NOVEL TERPHENYL COMPOUND

    Номер: KR20010110185A
    Принадлежит:

    PURPOSE: Provided is a novel terphenyl compound which has useful chiral liquid crystalline properties and is suitable for use in liquid crystal compositions. CONSTITUTION: The novel terphenyl compound is represented by formula 1. In the formula 1, each of R1 and R2 is the same or different and selected from the group consisting of alkyl, alkyloxy, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkylthio, alkenylthio, alkynylthio, and(where * indicates an asymmetric carbon atom), with the proviso that at least one of R1 and R2 is and ,each of R3 and R4 is the same or different and is an alkyl, alkenyl or alkynyl group, and Z is independently selected from hydrogen and fluorine at each terphenyl carbon. © KIPO 2002 ...

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    01-11-2012 дата публикации

    SULFUR-FREE POLYMER WHICH IS SUITABLE FOR USING A MIXTURE OF BIODIESEL OIL AND PETROLEUM-DERIVED FUEL OIL AND EFFECTIVE FOR IMPROVING LOW-TEMPERATURE PROPERTIES OF FUEL OIL

    Номер: KR1020120120045A
    Принадлежит:

    PURPOSE: A sulfur-free polymer is provided to improve low-temperature properties of a fuel oil, a fuel oil from plant or animal supply source, and a mixture of the fuel oil. CONSTITUTION: A sulfur-free polymer comprises a unit structure indicated in chemical formula 1 and chemical formula 2. In the polymers the molar ratio of the unit structures indicated in chemical formula 1 and chemical formula 2 is 100:1 - 2:1. In the chemical formulas, R^1 is a C8-22 alkyl group, preferably a C12-C16 alkyl group, R^2 is hydrogen or methyl, R^3 is -R^5(OR^6)nOR^7, R^5 and R^6 are the same or different, and are linear or branched C1-C8 alkylene group, n is an integer from 1-30, R^7 is C1-C4 alkyl group, and R^4 is hydrogen or methyl. COPYRIGHT KIPO 2013 ...

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    07-07-2017 дата публикации

    IMPROVEMENT IN POLYMERS

    Номер: KR1020170078579A
    Принадлежит:

    A ternary copolymer of the present invention is a high quality polymer, which comprises as a structural unit: a unit of chemical formula (I); a unit of chemical formula (II); a unit of chemical formula (IIIa) or (IIIb); and a unit of chemical formula (VII) arbitrarily, wherein the polymer improves high-temperature properties of fuel oil from oil resources, especially animal or vegetable materials. COPYRIGHT KIPO 2017 ...

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    13-07-2011 дата публикации

    Improvements in polymers

    Номер: CN0102120804A
    Принадлежит:

    The invention relates to improvements in polymers, wherein a terpolymer is a polymer having structural units, units of formula I, units of formula II and units of either formula IIIa or formula IIIb: The polymer improves the low-temperature properties of fuel oils from petroleum sources and especially from vegetable or animal sources.

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    24-06-2003 дата публикации

    BENZOFURAN COMPOUND

    Номер: JP2003176282A
    Принадлежит: Sharp Corp

    (57)【要約】 【課題】 エレクトロルミネッセンス材料のコアを変更 することによって、発光色と、高デバイス効率と高寿命 エレクトロルミネッセンス材料を提供すること。 【解決手段】 本発明の中間体エチニレン化合物を調製 する方法は、少なくとも1つの芳香環を含むコア部分お よびこれに共有結合した少なくとも3つの置換または非 置換のベンゾフラン基を含み、中間体エチニレン化合物 において、少なくとも3つのベンゼン環が各々コア部分 にエチニレン結合を介して結合し、各ベンゼン環が、オ ルト位においてブロックされたカルボニルオキシ基によ って置換されている工程、カルボニルオキシ基を脱ブロ ックする工程、上記脱ブロックされた基と隣接するエチ ニレン結合との間の反応によって環化反応を行い、ベン ゾフラン基のフラン環を形成することによって、分枝鎖 ベンゾフラン化合物を生成する工程を包含する。

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    31-03-2010 дата публикации

    Additives and lubricating oil compositions containing same

    Номер: CN0101687766A
    Принадлежит:

    Para-alkylated substituted diphenylamines are made by catalytically alkylating diphenylamine with a branched-chain alkene, such as propene, oligomer mixture in which the oligomer present in the greatest percentage has 15-24 carbon atoms. The alkylated diphenylamines are useful crankcase lubricant additives such as for reducing piston deposits and engine sludge.

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    12-02-2002 дата публикации

    NEW TERPHENYL COMPOUND

    Номер: JP2002047236A
    Принадлежит:

    PROBLEM TO BE SOLVED: To provide a new terphenyl compound preferably having a useful chiral liquid crystal property. SOLUTION: This terpenyl compound is represented by the general formula (1) (R1 and R2 are each the same or different and selected from the group consisting of alkyl, alkyloxy, alkenyl, alkenyloxy, alkynyl, alkynyloxy, alkylthio, alkenylthio and alkynylthio groups and the like; and Z is selected from H and F based on each terphenyl carbon independently). An example of the general formula (1) is 1,2-(S)-dimethoxy-(4"-octyloxyterphenyl-4-oxy)butane. COPYRIGHT: (C)2002,JPO ...

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    18-12-2008 дата публикации

    Additives and lubricating oil compositions containing same

    Номер: WO2008154334A1
    Принадлежит: Infineum International Limited

    Para-alkylated substituted diphenylamines are made by catalytically alkylating diphenylamine with a branched-chain alkene, such as propene, oligomer mixture in which the oligomer present in the greatest percentage has 15-24 carbon atoms. The alkylated diphenylamines are useful crankcase lubricant additives such as for reducing piston deposits and engine sludge.

    Подробнее
    23-12-1993 дата публикации

    Liquid crystal compounds, mixtures and devices

    Номер: WO1993025631A1

    According to this invention there are provided compounds having general formula (I), in which A1 is selected from alkyl, alkoxy or alkenyl; X1, X2, X3 and X4 are independently selected from the halogen group; m, n, p and q are independently 0, 1, 2, 3 or 4 such that m+n+p+q ¸ 0; Y is selected from O and COO; A2 is an end group of formula (II), where Z is selected from halogen, CH3, CN, CF3, CHF2; R is a linear or branched alkyl group or H; R1 is a linear or branched alkyl group or H.

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    10-04-1996 дата публикации

    Liquid crystal compounds, mixtures and devices

    Номер: EP0705318A1
    Принадлежит: UK Secretary of State for Defence

    According to this invention there are provided compounds having general formula (I), in which A1 is selected from alkyl, alkoxy or alkenyl; X1, X2, X3 and X4 are independently selected from the halogen group; m, n, p and q are independently 0, 1, 2, 3 or 4 such that m+n+p+q NOTEQUAL 0; Y is selected from O and COO; A2 is an end group of formula (II), where Z is selected from halogen, CH3, CN, CF3, CHF2; R is a linear or branched alkyl group or H; R1 is a linear or branched alkyl group or H.

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    24-02-2010 дата публикации

    Additives and lubricating oil compositions containing same

    Номер: EP2155657A1
    Принадлежит: Infineum International Ltd

    Para-alkylated substituted diphenylamines are made by catalytically alkylating diphenylamine with a branched-chain alkene, such as propene, oligomer mixture in which the oligomer present in the greatest percentage has 15-24 carbon atoms. The alkylated diphenylamines are useful crankcase lubricant additives such as for reducing piston deposits and engine sludge.

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    15-02-2012 дата публикации

    Polymer und polymerzusammensetzungen

    Номер: ATE542842T1
    Принадлежит: Infineum Int Ltd

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