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    • 82. 发明授权
    • Substituted quaterrylene tetracarboxylic acid diimides
    • 取代的四亚甲基四羧酸二酰亚胺
    • US6124458A
    • 2000-09-26
    • US335535
    • 1999-06-18
    • Klaus MuellenHeribert QuanteArno Bohm
    • Klaus MuellenHeribert QuanteArno Bohm
    • C07D221/18C07D471/06C09B5/62C09B57/08
    • C07D221/18C09B5/62
    • Quaterrylenetetracarboxylic diimides I whereR is hydrogen;C.sub.1 -C.sub.30 -alkyl whose carbon chain may be interrupted by one or more of --O--, --S--, --NR.sup.1 --, --CO-- and/or --SO.sub.2 -- and which may be monosubstituted or polysubstituted by cyano, C.sub.1 -C.sub.6 -alkoxy or a 5-, 6- or 7-membered heterocyclic radical which is attached via a nitrogen atom and which may contain further heteroatoms and may be aromatic, whereR.sup.1 is hydrogen or C.sub.1 -C.sub.6 -alkyl;C.sub.5 -C.sub.8 -cycloalkyl whose carbon skeleton may be interrupted by one or more of --O--, --S-- and/or --NR.sup.1 --;aryl or hetaryl, which may each be monosubstituted or poly-substituted by C.sub.1 -C.sub.18 -alkyl, C.sub.1 -C.sub.6 -alkoxy, cyano, --CONHR.sup.2, --NHCOR.sup.2 and/or aryl- or hetaryl-azo, which may each be substituted by C.sub.1 -C.sub.10 -alkyl, C.sub.1 -C.sub.6 -alkoxy or cyano, whereR.sup.2 is hydrogen; C.sub.1 -C.sub.18 -alkyl; aryl or hetaryl, which may each be substituted by C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen or cyano;X is halogen; C.sub.1 -C.sub.18 -alkyl; aryloxy, arylthio, hetaryloxy or hetarylthio, which may each be substituted by C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy;n is from 2 to 12,their preparation and use as pigments or fluorescent dyes and also substituted 9-haloperylene-3,4-dicarbimides III as intermediates therefor.
    • 四芳基四羧酸二酰亚胺I,其中R是氢; 其碳链可以被-O - , - S - , - NR 1 - , - CO - 和/或-SO 2 - 中的一个或多个中断的C 1 -C 30 - 烷基,并且其可以被氰基,C 1 -C 6单取代或多取代 - 烷氧基或5-,6-或7-元杂环基,其通过氮原子连接并且可以含有另外的杂原子并且可以是芳族的,其中R 1是氢或C 1 -C 6 - 烷基; 碳骨架可被-O - , - S-和/或-NR1-中的一个或多个中断的C 5 -C 8 - 环烷基; 芳基或杂芳基,其可以各自被C1-C18-烷基,C1-C6-烷氧基,氰基,-CONHR2,-NHCOR2和/或芳基 - 或杂芳基 - 偶氮基单取代或多取代,其可以各自被C1 -C 10 - 烷基,C 1 -C 6 - 烷氧基或氰基,其中R 2是氢; C1-C18-烷基; 芳基或杂芳基,其各自可被C 1 -C 6 - 烷基,C 1 -C 6 - 烷氧基,卤素或氰基取代; X是卤素; C1-C18-烷基; 芳氧基,芳硫基,杂芳氧基或杂芳硫基,其各自可被C 1 -C 4 - 烷基或C 1 -C 4 - 烷氧基取代; n为2至12,它们的制备和用作颜料或荧光染料,并且还取代了9-卤代亚烷基-3,4-二酰亚胺III作为其中间体。
    • 83. 发明授权
    • Process for the preparation of peryleneimides, novel di-, tri- and
tetrachromophoric perylene dyes and their use
    • 苝酰亚胺的制备方法,新型二 - ,三 - 和四 - 四氢苝染料及其用途
    • US5693808A
    • 1997-12-02
    • US554214
    • 1995-11-06
    • Heinz Langhals
    • Heinz Langhals
    • G02B5/22C07D471/06C08K5/3412C08K5/3437C08L101/00C09B5/62C09B57/08C09D11/50C09K9/02C09K11/06G03G5/06G03G9/09C07D471/04
    • C09D11/50C08K5/3437C09B5/62C09K11/06C09K9/02G03G5/0661G03G9/0906
    • Di-, tri- and tetrachromophoric perylene-3,4:9,10-tetracarboxylic acid imides of the formula I ##STR1## in which A is, for example, 1,4-phenylene, R is 1-hexylheptyl and m is 2, are readily accessible by reaction of a perylene-3,4:9,10-tetracarboxylic acid monoanhydride monoimide with 1,4-diaminobenzene-bisformamide. The preparation process and also a specific process for the preparation of monochromic perylene-3,4:9, 10-tetracarboxylic acid bisimides are also claimed. These processes are particularly suitable for reaction of highly electron-rich aromatic amines, which cannot be reacted under conventional condensation conditions. The compounds according to the invention are suitable, for example, as colouring agents for melt coloration of high molecular weight organic material, for use in security printing, as fluorescence dyes for machine-readable markings, as laser dyes and for the production of printing toners, colour filters, organic photoreceptors, electroluminescence and photoluminescence elements or solar collectors.
    • 其中A为例如1,4-亚苯基,R为1-己基庚基的式I(I)的二 - ,三 - 和四 - 四氢苝 - 3,4:9,10-四羧酸酰亚胺 m为2,可以通过苝-3,4:9,10-四羧酸单酐与1,4-二氨基苯 - 二甲酰胺的反应容易地进行。 还要求制备方法以及制备单色苝-3,4:9,10-四羧酸双酰亚胺的具体方法。 这些方法特别适用于在常规冷凝条件下不能反应的高电子富余芳族胺的反应。 根据本发明的化合物适用于例如作为高分子量有机材料的熔融着色的着色剂,用于安全印刷,作为用于机器可读标记的荧光染料,作为激光染料和用于印刷调色剂的生产 ,滤色器,有机感光体,电致发光和光致发光元件或太阳能收集器。
    • 84. 发明授权
    • Method for improving strength of dry dye particles and reducing
explosion hazards
    • 提高干燥染料颗粒强度并减少爆炸危险的方法
    • US4663859A
    • 1987-05-12
    • US784129
    • 1985-10-04
    • James W. HinsonDiane H. Roe
    • James W. HinsonDiane H. Roe
    • C09B57/08C09B67/00C09B67/06F26B3/08
    • C09B67/0095C09B67/0003
    • A process for preparing dry dye granules is disclosed. The process involves the preparation of a controlled moisture content slurry of the dye. Then introducing the slurry into a turbogranulator to form solid spherical particles whose size is controlled by the moisture content of the slurry. Then drying the particles in a fluidized bed dryer by heated air. Most of the fines are removed during the drying stage in the exit air stream from the dryer. The remaining fines and over sized particles are recovered on screening and are combined and ground and used to control the moisture content of the initial slurry. The final solid granules have good strength as compared to the previously marketed spray-dried materials which were in the form of porous hollow spheres. They are more readily dispersible and more rapidly dissolving.
    • 公开了制备干染料颗粒的方法。 该方法涉及制备染料的受控含水量浆液。 然后将浆料引入蒸发器中以形成固体球形颗粒,其尺寸由浆料的水分含量控制。 然后通过加热的空气在流化床干燥器中干燥颗粒。 在干燥器的出口空气流中的干燥阶段,大部分细粉被去除。 剩余的细粉和超大尺寸的颗粒在筛选中回收并合并并研磨并用于控制初始浆料的水分含量。 与以前销售的多孔中空球形喷雾干燥材料相比,最终的固体颗粒具有良好的强度。 它们更容易分散和更快速溶解。
    • 89. 发明授权
    • Process for the preparation of 4-amino-1,8-naphthalimides
    • 制备4-氨基-1,8-萘二酰亚胺的方法
    • US4172202A
    • 1979-10-23
    • US867705
    • 1978-01-09
    • Theodor Papenfuhs
    • Theodor Papenfuhs
    • C07D221/14C09B57/08
    • C07D221/14C09B57/08
    • N-substituted amides or optionally N-substituted hydrazides of 4-amino-naphthalic acids which may be substituted in 3-position by a sulfo group are obtained by reacting 4-halo-1,8-naphthalic anhydride with a primary amine or an optionally N-substituted hydrazine having a pK.sub.a -value of at least 8, exchanging in the so-obtained 4-halo-naphthalimide the halogen for the amino group by reacting it with ammonia and, optionally, subsequent sulfonation. The products are dyeing matters useful for the coloration of synthetic fibers, plastics, oils, waxes, resins, paper, printing pastes, lacquers or natural polyamides, especially for daylight-fluorescence pigments.
    • 通过4-卤代-1,8-萘二甲酸酐与伯胺或任选地,通过使4-卤代-1,8-萘二酸酐反应,可以通过磺基可以在3-位上被取代的N-取代酰胺或任选的N-取代的4-氨基 - 萘甲酸酰肼 具有pKa值至少为8的N-取代的肼,通过使其与氨反应,并任选地随后进行磺化,在如此获得的4-卤代萘酰亚胺中交换卤素的氨基。 该产品是用于合成纤维,塑料,油,蜡,树脂,纸,印刷浆,漆或天然聚酰胺着色的染色物质,特别是用于日光荧光颜料。