Triazolopyridine dyes
    2.
    发明授权
    Triazolopyridine dyes 失效
    三唑并吡啶染料

    公开(公告)号:US5616710A

    公开(公告)日:1997-04-01

    申请号:US687453

    申请日:1996-08-19

    摘要: Triazolopyridine dyes of the formula ##STR1## where one of the two radicals A and E is nitrogen and the other is a radical of the formula C-R.sup.1, where R.sup.1 is unsubstituted or substituted C.sub.1 -C.sub.20 -alkyl, unsubstituted or substituted phenyl or unsubstituted or substituted mercapto,Q is a radical of the formula ##STR2## where R.sup.2 is a carbocyclic or heterocyclic radical,R.sup.3 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxycarbonyl or unsubstituted or substituted phenyl,R.sup.4 is cyano, carbamoyl, carboxyl, C.sub.1 -C.sub.4 -alkoxycarbonyl or benzothiazolyl or R.sup.3 and R.sup.4 together are the remainder of a fused-on benzene ring andX is CH or nitrogen, andR.sup.5 is oxygen or a radical of a compound with an acidic CH, and a process for the thermal transfer of these dyes.

    摘要翻译: PCT No.PCT / EP95 / 00564 Sec。 371日期:1996年8月19日 102(e)日期1996年8月19日PCT提交1995年2月15日PCT公布。 第WO95 / 22581号公报 日期1995年8月24日具有式(IMAGE)的三唑并吡啶染料,其中两个基团A和E中的一个是氮,另一个是式C-R 1的基团,其中R 1是未取代的或取代的C 1 -C 20 - 烷基, 或取代的苯基或未取代的或取代的巯基,Q是下式的基团,其中R 2是碳环或杂环基,R 3是未取代的或取代的C 1 -C 4 - 烷基,C 1 -C 4 - 烷氧基羰基或未取代的或未取代的 取代的苯基,R 4是氰基,氨基甲酰基,羧基,C 1 -C 4 - 烷氧基羰基或苯并噻唑基,或者R 3和R 4一起是稠合的苯环的其余部分,X是CH或氮,R 5是氧或化合物 具有酸性CH,以及这些染料的热转移过程。

    Triazolopyridine dyes and intermediates therefor
    4.
    发明授权
    Triazolopyridine dyes and intermediates therefor 失效
    三唑并吡啶染料及其中间体

    公开(公告)号:US5700757A

    公开(公告)日:1997-12-23

    申请号:US597559

    申请日:1996-02-02

    摘要: Triazolopyridine dyes of the formula ##STR1## where R.sup.1 is unsubstituted or substituted C.sub.1 -C.sub.20 -alkyl, unsubstituted or substituted phenyl, unsubstituted or substituted hydroxyl or unsubstituted or substituted mercapto, Q is a radical of the formula ##STR2## where R.sup.2 is a carbocyclic or heterocyclic radical, R.sup.3 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, R.sup.4 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy, R.sup.5 is unsubstituted or substituted C.sub.1 -C.sub.8 -alkyl, unsubstituted or substituted phenyl, unsubstituted or substituted thienyl or unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy, or the radical CR.sup.3 R.sup.4 R.sup.5 together is C.sub.3 -C.sub.7 -cycloalkyl, C.sub.1 -C.sub.4 -haloalkyl, unsubstituted or substituted phenyl or unsubstituted or substituted thienyl, R.sup.6 is cyano, carbamoyl, carboxyl, C.sub.1 -C.sub.4 -alkoxycarbonyl or benzothiazolyl, and E is CH or nitrogen, and R.sup.7 is oxygen or a radical of an acidic--CH compound, a process for the thermal transfer of these dyes, their use for dyeing or printing synthetic materials and also triazolopyridines as intermediates for these dyes.

    摘要翻译: 其中R 1是未取代的或取代的C 1 -C 20烷基,未取代或取代的苯基,未取代或取代的羟基或未取代或取代的巯基的三唑并吡啶染料,其中R 2是碳环 或杂环基,R 3为氢或未取代或取代的C 1 -C 4 - 烷基,R 4为氢,未取代或取代的C 1 -C 4 - 烷基或C 1 -C 4 - 烷氧基,R 5为未取代或未取代或未取代的C 1 -C 8 - 苯基,未取代或取代的噻吩基或未取代或取代的C 1 -C 4 - 烷氧基,或基团CR 3 R 4 R 5一起为C 3 -C 7 - 环烷基,C 1 -C 4 - 卤代烷基,未取代或取代的苯基或未取代或取代的噻吩基,R 6为氰基,氨基甲酰基, 羧基,C 1 -C 4 - 烷氧基羰基或苯并噻唑基,E是CH或氮,R 7是氧或酸性-CH化合物的基团,这些染料的热转移过程,它们用于染色或印刷合成 以及作为这些染料的中间体的三唑并吡啶类。

    Naphtholactam dyes
    5.
    发明授权
    Naphtholactam dyes 失效
    萘酚内酰胺染料

    公开(公告)号:US5929245A

    公开(公告)日:1999-07-27

    申请号:US776596

    申请日:1997-02-18

    摘要: The invention concerns naphtholactam derivatives of formula (I), in which: R.sup.1 represents hydrogen, optionally substituted C.sub.1 -C.sub.6 alkyl C.sub.5 -C.sub.6 cycloalkcyl or substituted phenyl; R.sup.2 and R.sup.3 represent hydrogen, C.sub.1 -C.sub.8 alkanoyl, optionally substituted benzoyl, optionally substituted C.sub.2 -C.sub.4 alkyl, optionally substituted C.sub.2 -C.sub.4 alkenyl, optionally substituted C.sub.2 -C.sub.4 alkinyl, a halogen, nitro, sulphamoyl, optionally substituted hydroxy, optionally substituted mercapto, C.sub.1 -C.sub.6 alkysulphonyl or optionally substituted phenylsulphonyl; R.sup.4 represents hydrogen or, with R.sup.3, a group of formula (II); R.sup.5 represents hydrogen or C.sub.1 -C.sub.6 alkyl; R.sup.6 represents cyano, carbamoyl, C.sub.1 -C.sub.4 mono- or dialkylcarbamoyl carboxyl or C.sub.1 -C.sub.4 alkoxycarbonyl; and R.sup.7 represents substituted C.sub.1 -C.sub.4 alkyl, optionally substituted C.sub.5 -C.sub.13 alkyl or benzoyl. Also disclosed is the use of these derivatives for dyeing or printing textiles.

    摘要翻译: PCT No.PCT / EP95 / 03112 Sec。 371日期1997年2月18日 102(e)日期1997年2月18日PCT提交1995年8月4日PCT公布。 公开号WO96 / 06137 日期:1996年2月29日本发明涉及式(I)的萘内酰胺衍生物,其中:R 1表示氢,任选取代的C 1 -C 6烷基C 5 -C 6环烷基或取代的苯基; R 2和R 3表示氢,C 1 -C 8烷酰基,任选取代的苯甲酰基,任选取代的C 2 -C 4烷基,任选取代的C 2 -C 4烯基,任选取代的C 2 -C 4炔基,卤素,硝基,氨磺酰基,任选取代的羟基,任选取代的巯基 ,C 1 -C 6烷磺酰基或任选取代的苯基磺酰基; R4表示氢,或与R3表示式(Ⅱ)的基团。 R5表示氢或C1-C6烷基; R6表示氰基,氨基甲酰基,C1-C4单或二烷基氨基甲酰基羧基或C1-C4烷氧基羰基; 并且R 7表示取代的C 1 -C 4烷基,任选取代的C 5 -C 13烷基或苯甲酰基。 还公开了这些衍生物用于染色或印花纺织品的用途。

    Use of 4-cyano-naphthalene-1, 8-dicarboximide derivatives and related compounds to protect organic material from the damaging effects of light
    7.
    发明申请
    Use of 4-cyano-naphthalene-1, 8-dicarboximide derivatives and related compounds to protect organic material from the damaging effects of light 有权
    使用4-氰基 - 萘-1,8-二羧酰亚胺衍生物和相关化合物来保护有机材料免受光的破坏作用

    公开(公告)号:US20070100033A1

    公开(公告)日:2007-05-03

    申请号:US10579441

    申请日:2004-11-12

    IPC分类号: C08K5/34

    CPC分类号: C07D221/14

    摘要: A description is given of the use of naphthalene-1,8-dicarboxylic monoimides of the formula (I), in which R1 is hydrogen, alkyl, alkenyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl or heteroaryl and R2 is a radical containing at least one π electron system containing a carbon atom and at least one further atom selected from carbon, oxygen, and nitrogen, with the proviso that the radical contains at least one atom other than carbon; to protect organic material from the damaging effects of light, of compositions which comprise at least one naphthalene-1,8-dicarboxylic monoimide of the formula (I) in an amount which provides protection from the damaging effects of light, and at least one organic material, and of new naphthalene-1,8-dicarboxylic monoimides (I).

    摘要翻译: 描述了使用式(I)的萘-1,8-二羧酸单酰亚胺,其中R 1是氢,烷基,烯基,环烷基,环烯基,杂环烷基,芳基或杂芳基 并且R 2是含有至少一个含有碳原子和至少一个选自碳,氧和氮的另外的原子的π电子体系的基团,条件是该基团含有至少一个原子 除碳外; 以保护有机材料免受光的破坏性影响,所述组合物包含至少一种式(I)的萘-1,8-二羧酸单酰亚胺,其量提供防止光的破坏作用,以及至少一种有机物 材料和新的萘-1,8-二羧酸单酰亚胺(I)。

    Method for Determining the Identity, Absence and Concentration of a Chemical Compound in a Medium

    公开(公告)号:US20090006004A1

    公开(公告)日:2009-01-01

    申请号:US12159005

    申请日:2006-12-27

    IPC分类号: G01N21/00

    摘要: A method is proposed for detecting at least one chemical compound V contained in a medium (312). The method comprises a verification step (420) which is used to determine whether V is contained in the medium (312). The method furthermore comprises an analysis step (424) in which a concentration c of the at least one chemical compound V is determined.The verification step comprises the following substeps: (a1) the medium (312) is exposed to a first analysis radiation (316) of a variable wavelength λ, the wavelength λ assuming at least two different values; (a2) at least one spectral response function A(λ) is generated with the aid of the radiation (324) absorbed and/or emitted and/or reflected and/or scattered by the medium (312) in response to the first analysis radiation (316); (a3) at least one spectral correlation function K(δλ) is formed by spectral comparison of the at least one spectral response function A(λ) with at least one pattern function R(λ+δλ), the at least one pattern function R(λ) representing a spectral measurement function of a medium (312) containing the chemical compound V and δλ being a coordinate shift; (a4) the at least one spectral correlation function K(δλ) is examined in a pattern recognition step (418), and a conclusion is made as to whether the at least one chemical compound V is contained in the medium (312); The analysis step (424) comprises the following substeps: (b1) the medium (312) is exposed to at least one second analysis radiation (318) having at least one excitation wavelength λEX; (b2) at least one spectral analysis function B(λEX,λRES) is generated with the aid of the radiation (326) of the response wavelength λRES absorbed and/or emitted and/or reflected and/or scattered by the medium (312) in response to the second analysis radiation (318) of the wavelength λEX and the concentration c is deduced therefrom.