利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

15 条记录 (耗时 0.013 秒)

    Benzthiazolyl-azo-indole basic dyestuffs
    1.
    发明授权
    Benzthiazolyl-azo-indole basic dyestuffs 失效
    苯并噻唑基 - 偶氮 - 吲哚碱性染料

    公开(公告)号：US4252716A

    公开(公告)日：1981-02-24

    申请号：US39105

    申请日：1979-05-15

    申请人： Hans-Peter Kuhlthau

    发明人： Hans-Peter Kuhlthau

    IPC分类号： C08K5/00 ,  C08K5/45 ,  C08K5/47 ,  C08L1/00 ,  C08L27/00 ,  C08L33/00 ,  C08L33/02 ,  C08L67/00 ,  C08L77/00 ,  C09B23/16 ,  C09B27/00 ,  C09B29/40 ,  C09B43/11 ,  C09B44/20 ,  D06P3/32 ,  C09B29/22 ,  C09B29/36 ,  C09B31/14

    CPC分类号： C09B23/16 ,  C09B27/00 ,  C09B44/20

    摘要： Basic dyestuffs of the formula ##STR1## Wherein R.sub.2 denotes a non-ionic substituent,R.sub.3, R.sub.4 denote alkyl, alkenyl, cycloalkyl or aralkyl,R.sub.5 denotes hydrogen, alkyl, cycloalkyl or aryl,R.sub.6 denotes hydrogen or alkyl, and R.sub.5 and R.sub.6 can together complete a cycloalkyl ring,R.sub.7 denotes hydrogen or alkyl, and R.sub.6 and R.sub.7 can together complete a cycloalkyl ring,R.sub.8 denotes a non-ionic substituent or a carboxyl group,p denotes the numbers 0, 1, 2, 3 or 4,n denotes the numbers 0, 1, 2 or 3 andX.sup.- denotes an anion,are suitable for dyeing and printing of natural and synthetic materials, particularly of polyacrylonitrile, copolymers of acrylonitrile with other vinyl compounds of acid modified polyesters and acid modified polyamides.

    摘要翻译： 式（Ⅰ）的基本染料其中R2表示非离子取代基，R3，R4表示烷基，烯基，环烷基或芳烷基，R5表示氢，烷基，环烷基或芳基，R6表示氢或烷基，R5表示 并且R 6可以一起完成环烷基环，R 7表示氢或烷基，R 6和R 7可以一起完成环烷基环，R 8表示非离子取代基或羧基，p表示数字0,1,2,3或 4，n表示数字0,1,2或3，X表示阴离子，适用于天然和合成材料，特别是聚丙烯腈，丙烯腈与酸改性聚酯的其他乙烯基化合物的共聚物和酸改性的染色和印刷 聚酰胺。

    Basic azo dyestuffs containing a benzthiazole and a tetrahydroquinoline nucleus
    2.
    发明授权
    Basic azo dyestuffs containing a benzthiazole and a tetrahydroquinoline nucleus 失效
    含有苯并噻唑和四氢喹啉核的碱性偶氮染料

    公开(公告)号：US3991042A

    公开(公告)日：1976-11-09

    申请号：US414181

    申请日：1973-11-09

    申请人： Hans-Peter Kuhlthau

    发明人： Hans-Peter Kuhlthau

    IPC分类号： C08K5/00 ,  C08K5/45 ,  C08L33/00 ,  C08L33/02 ,  C08L67/00 ,  C08L77/00 ,  C09B23/16 ,  C09B27/00 ,  C09B29/44 ,  C09B44/20 ,  C09B29/36 ,  C09B43/00

    CPC分类号： C09B23/16 ,  C09B27/00 ,  C09B44/20

    摘要： Basic dyestuffs of the formula ##SPC1##WhereinR.sub.2 denotes a non-ionic substituent,R.sub.3 denotes alkyl, alkenyl, cycloalkyl or aralkyl,R.sub.4 denotes hydrogen, alkyl, alkenyl, cycloalkyl or aralkyl,R.sub.5 denotes a non-ionic substituent or a carboxyl group,P denotes the numbers 0, 1, 2, 3 or 4,N denotes the numbers 0, 1, 2 or 3 andX.sup.- denotes an anion in which A and B can be fused to other rings and in which the cyclic and acyclic radicals can contain non-ionic substituents or carboxyl groups as well as mixtures of such dyestuffs are disclosed. The dyestuffs are suitable for dyeing and printing of natural and synthetic materials, particularly of polyacrylonitrile, copolymers of acrylonitrile with other vinyl compounds, of acid modified polyesters and acid modified polyamides.

    摘要翻译： 式WHEREIN R2表示非离子取代基的基本染料，R3表示烷基，烯基，环烷基或芳烷基，R4表示氢，烷基，烯基，环烷基或芳烷基，R5表示非离子取代基或羧基，P DENOTES 数字0,1,2,3或4，N表示数字0,1,2或3，X'表示其中A和B可以与其它环稠合并且其中环状和非环状基团的阴离子 可以含有非离子取代基或羧基以及这些染料的混合物。 该染料适用于天然和合成材料，特别是聚丙烯腈，丙烯腈与其它乙烯基化合物的共聚物，酸改性聚酯和酸改性聚酰胺的染色和印花。

    Bis-type quaternary salts including benzothiazole and benzimidazole rings and process for preparing dye therewith
    3.
    发明授权
    Bis-type quaternary salts including benzothiazole and benzimidazole rings and process for preparing dye therewith 失效
    包括苯并噻唑和苯并咪唑环的双型季盐及其制备染料的方法

    公开(公告)号：US3976640A

    公开(公告)日：1976-08-24

    申请号：US550182

    申请日：1975-02-18

    申请人： Alan L. Borror ,  Louis Cincotta

    发明人： Alan L. Borror ,  Louis Cincotta

    IPC分类号： C07D235/08 ,  C09B23/06 ,  C09B23/16 ,  G03C1/14 ,  C07D417/12 ,  C07D417/06

    CPC分类号： C09B23/06 ,  C07D235/08 ,  C09B23/16 ,  G03C1/14

    摘要： Novel bis type heterocyclic quaternary salts are provided which are useful in the preparation of various linked cyanine dyes and related compounds.BACKGROUND OF THE INVENTION1. Field of the InventionThis invention relates to chemistry and, more particularly, to novel double or "bis-type" quaternary salts of heterocyclic bases and processes useful in the synthesis of various linked cyanine dyes and related compounds.2. Description of the Prior ArtMost of the reactions leading to cyanine dyes and those compounds related to them are of the condensation type wherein two active dye intermediates react under suitable conditions with the elimination of some simple molecule, such as mineral acid, mercaptan, alcohol, water, aniline or acetanilide. These intermediates fall into two categories: (1) those containing reactive hydrogen, and (2) those containing a reactive group, such as halogen, cyano, alkyl- or arylmercapto, alkoxy, anilino, or acetanilido, which is capable of dye condensation with the reactive hydrogen of the first component.In the synthesis of "true" cyanine materials, intermediates of the first type are usually quaternary salts of heterocyclic bases containing a reactive methyl group, which react through the formation of a methylene base resulting from the loss of a proton. Components of the second type are also frequently quaternary salts of heterocyclic bases, but having a proton seeking (negative) atom or group linked to the .alpha.- or .gamma.-atom of the heterocyclic nucleus either directly or through a vinylene or polyvinylene chain. In another type of reaction, two equivalents of the above-mentioned heterocyclic quaternary salt having a reactive methyl group may be condensed together through a component which provides the central part of the conjugated chain, e.g., ethyl orthoformate, giving rise to a symmetrical cyanine dye molecule.In compounds related to the cyanines, e.g., those dyestuffs containing an amidinium ion or amidic chromophoric system, only one of the above-mentioned types of intermediate may comprise a heterocyclic quaternary salt. For example, hemicyanine materials may be prepared by treating a heterocyclic quaternary salt having one of the aforementioned reactive negative substituents with an aromatic or an aliphatic amine containing the replaceable hydrogen, or p-dialkylaminostyryl dyes may be prepared by condensation of the appropriate heterocyclic quaternary salt containing a reactive methyl group with p-dialkylamino-benzaldehyde.Intermediates in the synthesis of cyanine dyes comprising at least two quaternary heterocyclic cyanine dye nuclei linked by a divalent hydrocarbon radical have previously been described in the art, for example, see U.S. Pat. Nos. 2,393,351; 2,425,772; 2,425,773; 2,461,139; 2,465,744; 2,592,196; and 3,622,317. These intermediates are disclosed as being useful in the synthesis of bis, polymeric or pseudopolymeric cyanine dyes, and are generally characterized as having a hydrocarbon linking moiety, e.g., an alkylene group, connecting the quaternized nitrogens of similar heterocyclic nuclei. These bis-type quaternary salts of the prior art are to be distinguished from those of the present invention in that the present compounds comprise an amide bond linking moiety between the cyanine dye segments, and said moiety is not attached to the quaternized nitrogens. In general, the compounds of this invention are more readily synthesized in better yields by virtue of the aforementioned amide linking moiety than bis-type quaternary salts of the prior art.SUMMARY OF THE INVENTIONIn accordance with the present invention, novel bis-type quaternary salts are provided which may be employed in the synthesis of a wide variety of linked cyanine dyes and related compounds. In general, the novel compounds of the invention comprise two linked heterocyclic quaternary salt segments, each containing a reactive methyl group in alpha or gamma position to the quaternary nitrogen atoms of the respective nuclei. The segments are linked together through a novel amide containing bridging group attached at each end to a nuclear atom other than the quaternized nitrogen of the salt segment.The alkylene-amide bridging or linking group is particularly advantageous over linking groups employed in previous bis-type quaternary salts in that the individual heterocyclic segments are readily joined through the formation of an amide bond, the length of the chain is easily changed to suit particular needs and the group is stable throughout the various dye condensation reactions employed to form cyanine dyes and related compounds. Since each heterocyclic salt segment includes a reactive methyl substituent, the novel bis-type compounds of the invention may be condensed with the appropriate conventional dyestuff intermediates to provide a wide variety of linked cyanine dyes and related materials.The novel compounds of the invention may be represented by one of the formulae: ##SPC1## ##SPC2##wherein R is an alkylene group having from 1 to 5 carbon atoms, e.g., --(CH.sub.2).sub.2 --, --(CH.sub.2).sub.3 --, etc.; A is a divalent amide group, i.e., ##STR1## R.sup.1 and R.sup.2 are each a lower alkyl group, i.e., a 1 to 4 carbon alkyl group such as methyl, ethyl, etc., a sulfoalkyl group, e.g., sulfpropyl, sulfobutyl, etc., or a carboxyalkyl group, e.g., carboxymethyl, carboxyethyl, etc.; W is S or N--T wherein T is a lower alkyl group; X is a hydrogen atom, halogen atom, e.g., chloro, bromo, fluoro, etc., cyano group or a carbalkoxy group, e.g., carbmethoxy, carbpropoxy, etc.; Y is an acid anionic radical, e.g., haide, p-toluenesulfonate, etc.; n and p are each 0, 1 or 2; and m is 1 or 2.DETAILED DESCRIPTION OF THE INVENTIONIt should be understood that all formulae set forth herein, such as Formulae I and II above, represent only an illustration of one form of structure, and that the actual structure of the depicted compound may in fact be a resonance hybrid of a series of structures in accordance with known principles in the art. Hence, a bis-type quaternary salt of Formula I or Formula II might actually have one or two ternary nitrogen atoms, depending upon the distribution of double and single bonds in the structure, and other structures shown herein as being charged may in fact show a resonance between a charged and uncharged structure. Since the term "bis" denotes a completely symmetrical molecule, the compounds of the present invention are characterized as "bis-type" because each quaternary salt segment need not be the same, as shown in Formulae I and II.As examples of suitable substituents P.sup.1 and R.sup.2, mention may be made of lower alkyl groups (1 to 4 carbon alkyl groups) such as methyl, ethyl, propyl, isopropyl, butyl, and isobutyl; carboxyalkyl groups such as carboxymethyl, .alpha.-carboxyethyl, .beta.-carboxyethyl, .gamma.-carboxypropyl, .delta.-carboxybutyl, etc.; and sulfoalkyl groups such as sulfomethyl, .beta.-sulfoethyl, .gamma.-sulfopropyl, .delta.-sulfobutyl, p-sulfobenzyl, etc.Y represents the anionic acid radical or radicals customarily employed in the cyanine dye art to balance the positive change of the quaternary nitrogen such as, for example, halide, i.e., chloride, bromide, iodide; methylsulfate; p-toluenesulfonate; benzenesulfonate; acetate; propionate; cyanate; perchlorate; etc. When subscript p is 2, Y represents the two anionic radicals necessary to satisfy the positive charges on the quaternary nitrogen atoms of each heterocyclic salt segment. The individual heterocyclic segments may also exhibit an "internal salt" or "zwitterion" form wherein the anion takes the form of a negatively charged group in substituent R.sup.1 or R.sup.2, e.g., --SO.sub.3.sup..crclbar. or --COO.sup..crclbar.. In the latter case, there may be no external anion (p=0) or one external anion (p=1) depending upon whether one or both heterocyclic segments exhibit the internal salt form.The length of the linking chain between heterocyclic salt segments may be varied depending on the value of n, that is, the number of amide and alkylene groups in the chain, and on the number of carbon atoms in the alkylene groups. Longer linking chains may tend to decrease the solubility of the compound and also may decrease the efficiency of photon excited energy transfer through the molecule, whereas shorter chains may tend to increase any steric hinderance problems during synthesis of the various dye derivatives. Preferably, n is limited to 1 or 2, with the size of the alkylene group R ranging from 1 to 5 carbon atoms.As specific examples of some preferred bis-type quaternary salts within the scope of this invention, mention may be made of the following compounds, which are listed for the purposes of illustration and are not intended to limit the invention: ##SPC3##The novel compounds of the invention are readily prepared by reacting in a known and conventional manner, a primary amino-substituted quaternary salt of the formula: ##SPC4##with a carboxylic acid-substituted quaternary salt of the formula: ##SPC5##wherein all moieties are as defined for Formulae I and II.The length of the linking group may be built up by conventional chemical reactions prior to the above linking reaction. To illustrate, a representative synthesis of a preferred compound is set forth below without intending to limit the invention to the details set forth therein.

    摘要翻译： 提供了新的双杂环季盐，其可用于制备各种连接的花青染料和相关化合物。

    Dye salts
    9.
    发明授权
    Dye salts 失效
    染色盐

    公开(公告)号：US4439204A

    公开(公告)日：1984-03-27

    申请号：US412741

    申请日：1982-08-30

    申请人： Willy Stingelin ,  Peter Loew

    发明人： Willy Stingelin ,  Peter Loew

    IPC分类号： D01F1/06 ,  C09B23/16 ,  C09B69/02 ,  C09B69/06 ,  C08K5/34

    CPC分类号： C09B23/16 ,  C09B69/06 ,  Y10S8/927

    摘要： The novel dye salts of the formula ##STR1## wherein Z, B, X, m and n are as defined in claim 1, are suitable for dyeing polyacrylonitrile in the spinning dope. The fibres dyed according to the invention have good fastness to rubbing, steaming, washing and light.

    摘要翻译： 其中Z，B，X，m和n如权利要求1所定义的式IMA图像的新型染料盐适用于在纺丝原液中染色聚丙烯腈。 根据本发明染色的纤维具有良好的摩擦，蒸汽，洗涤和光的牢度。