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PHOTOGRAPHIC SILVER HALIDE ELEMENTS USEFUL IN COLOUR DIFFUSION TRANSFER PROCESSES

机译:彩色扩散转移过程中常用的照相卤化银元素

摘要

1464104 Photographic silver halide material EASTMAN KODAK CO 28 Jan 1974 [26 Jan 1973] 03800/74 Heading G2C A photographic material comprises a support and a silver halide emulsion, the emulsion having associated therewith in a layer which is permeable to an alkaline aqueous processing composition a compound of the Formula:- where RSP1/SP is an aromatic ring; each of RSP2/SP and RSP3/SP is a bivalent organic group containing 1-3 atoms in the bivalent linkage; each of n and m is 1 or 2; Nu is an oxidizable nucleophilic group, i.e. an atom or group of atoms which have an electron pair capable of forming a covalent bond and which can be oxidized by oxidized silver halide developing agent, or a hydrolyzable precursor therefor; E is CO or SO 2 ; Q is a bivalent group providing a mono atom linkage between E and X 2 where the mono atom is a non-metallic atom of group VA or VIA of the MendelÚef periodic table in its 2- or 3- valence state; one of X 1 and Q-X 2 is a ballasting group of a size sufficient to render the compound immobile in the presence of the composition and the other of Xi and Q-X 2 is a photographically active moiety; Nu, RSP1/SP, RSP2/SP, RSP3/SP, m and n being selected to provide such proximity of Nu and E as to permit intramolecular nucleophilic displacement reaction, i.e. a reaction in which a nucleophilic centre attached to a compound reacts at another site on the compound which is an electrophilic centre, to effect displacement of a group or atom attached to the electrophilic centre, and to provide 3-5 atoms between the atom which is the nucleophilic centre of the nucleophilic group and the atom which is the electrophilic centre of E whereby the compound is capable of forming a 5- to 7- membered ring on the displacement reaction, the displacement reaction taking place in the presence of the composition and resulting in cleavage of Q-X 2 from E, and the nucleophilic group being selected so that the rate of oxidation thereof by oxidized silver halide developing agent is greater than the rate of intramolecular nucleophilic displacement and the oxidation of the nucleophilic group preventing the nucleophilic displacement reaction, whereby, after imagewise exposure, processing of the material with the composition in the presence of the silver halide developing agent produces imagewise release of the moiety. RSP1/SP may be a benzene ring and Nu a hydrolyzable precursor for a nucleophilic group of Formula -NRSP4/SP-O-CO- which is bonded through the -CO- group to the aromatic ring to form a 2,1- benzoisooxazolone of the Formula:- where RSP4/SP is optionally substituted alkyl having 1-10C or optionally substituted aryl having 6-20C or an alkali-hydrolyzable group; and m is 1. The compounds I to VIII specified are all azo dyes of the latter Formula where RSP4/SP is CH 3 , X 1 is C 18 H 37 N(CH 3 )CO- or C 18 H 37 O-, n is 1, E is CO, Q is -N(CH3)- and X 2 is the azo dye containing moiety which is released imagewise as above. A colour image may be provided by the dye released in a diffusion transfer process, or by the immobile dye remaining in the initial location attached to the oxidized compound or both images can be used. In addition Examples 8 and 9 disclose compounds of the above Formula C- 1 and C-2 having releasable colour coupler and oxichromic moiety respectively used to form negative and positive dye images. The silver and silver halide remaining after development may be removed. The silver bromide grain size is specified in the Examples. The photographically active moiety may be a silver complexing agent, silver halide solvent,.toner, hardener, antifoggant, foggant, sensitizer, desensitizer, developer, oxidizing agent, development inhibitor, or development accelerator but no compounds containing these moieties are specified. In Example 4 the red-sensitive silver halide emulsion contains a magenta dye imageproviding compound of the above Formula.
机译:1464104照相卤化银材料EASTMAN KODAK CO 1974年1月28日[1973年1月26日] 03800/74标题G2C照相材料包括载体和卤化银乳剂,该乳剂具有与之结合的可渗透碱性水处理组合物的层式为-的化合物:其中R 1 为芳环; R 2 和R 3 分别是在二价键中含有1-3个原子的二价有机基团。 n和m分别为1或2; Nu是可氧化的亲核基团,即具有能够形成共价键的电子对并且可以被氧化的卤化银显影剂或可水解的前体氧化的原子或原子团; E是CO或SO 2; Q是在E和X 2之间提供单原子键的二价基团,其中该单原子是孟德尔夫元素周期表的VA或VIA族的2价或3价态的非金属原子; X 1和Q-X 2中的一个是镇重基团,其大小足以使该化合物在组合物存在下不动,而Xi和Q-X 2的另一个是照相活性部分。选择Nu,R 1 ,R 2 ,R 3 ,m和n以提供Nu和E的接近度以允许分子内亲核置换反应,即连接到化合物的亲核中心在化合物的另一个位点(即亲电中心)反应,以实现连接到亲电中心的基团或原子的置换,并在它们之间提供3-5个原子的反应作为亲核基团的亲核中心的原子和作为E的亲电中心的原子,由此化合物能够在置换反应上形成5至7元环,置换反应在存在下进行组成并导致QX 2从E上裂解,并选择亲核基团,以使其被氧化卤化银显影剂的氧化速率大于分子内亲核取代速率和亲核基团的氧化速率。进行亲核取代反应,从而在成像曝光后,在卤化银显影剂存在下用该组合物处理该材料产生该成像部分的释放。 R 1 可以是苯环,Nu是式-NR 4 -O-CO-的亲核基团的可水解前体,该亲核基团通过-CO-基团键合至芳环形成下式的2,1-苯并异恶唑酮:其中R SP 4 =具有1-10C的任选取代的烷基或具有6-20C或碱可水解基团的任选取代的芳基;和m为1。所指定的化合物I至VIII为后一种式中的所有偶氮染料,其中R 4 为CH 3,X 1为C 18 H 37 N(CH 3)CO-或C 18 H 37 O-,n为1,E为CO,Q为-N(CH 3)-,X 2为含偶氮染料的部分,其如上所述成像释放。彩色图像可以由在扩散转移过程中释放的染料提供,也可以由残留在固定在氧化化合物上的初始位置的固定染料提供,或者可以使用两种图像。另外,实施例8和9公开了具有分别用于形成负染料图像和正染料图像的可脱色的成色剂和显色部分的上式C-1和C-2的化合物。显影后残留的银和卤化银可以除去。实施例中规定了溴化银的粒度。照相活性部分可以是银络合剂,卤化银溶剂,调色剂,硬化剂,防雾剂,雾化剂,敏化剂,脱敏剂,显影剂,氧化剂,显影抑制剂或显影促进剂,但未指定包含这些部分的化合物。在实施例4中,红敏卤化银乳剂含有上式的品红色染料图像提供化合物。

著录项

  • 公开/公告号GB1464104A

    专利类型

  • 公开/公告日1977-02-09

    原文格式PDF

  • 申请/专利权人 EASTMAN KODAK CO;

    申请/专利号GB19740003800

  • 发明设计人

    申请日1974-01-28

  • 分类号G03C5/54;

  • 国家 GB

  • 入库时间 2022-08-22 23:42:52

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