http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0141920-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C8-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B29-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C8-10
filingDate 1984-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d34a4849b1cc0be1724be778eb52800
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3304144ce2b2cde8b71ad060c56b7982
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d29952900057735190d6d31e442f9cc9
publicationDate 1985-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0141920-A2
titleOfInvention Colour-photographic recording material with dye-releasing compounds releasing 6-aryl-azo-2-amino-3 pyridinol dyes forming chelates with metal ions, and a colour picture with an image-wise distribution of nickel complexes of the dyes
abstract Q den zur Vervollständigung einer gegebenenfalls substituierten Phenyl- oder Naphthylgruppe erforderlichen Rest;n R° H oder Alkyl; R 1 einen aliphatischen, araliphatischen oder carbocyclisch oder heterocyclisch aromatischen Rest oder falls X die Gruppe-SO 2 -NR°-bedeutet, Wasserstoff. Dyes of the formula 1 are released imagewise from corresponding dye releasers in color diffusion transfer processes. With nickel ions they form light-fast blue-green dye-metal complexes with favorable spectral properties: in what mean Q is the residue necessary to complete an optionally substituted phenyl or naphthyl group; R ° H or alkyl; R 1 is an aliphatic, araliphatic or carbocyclic or heterocyclic aromatic radical or, if X denotes the group —SO 2 —NR ° —hydrogen.
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priorityDate 1983-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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