http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0651893-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03627f82d4edc6567f9627df6efdde5d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03F7-022
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03F7-022
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L21-027
filingDate 1993-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5787b65fcec3112c8c507c5f3a720ba1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_91b51c8b212183e24f0ca381771cbc0e
publicationDate 1995-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0651893-A1
titleOfInvention Hexahydroxybenzophenone sulfonate esters of diazonaphthoquinone sensitizers and positive photoresists employing same
abstract Positive photoresists formulations for producing positive photoresist images have improved thermal stability yet which allow a wide variation in resin to photoactive sensitizer compound without significant changes in photospeed, thermal behaviour, contrast or resolution and with virtually no less in unexposed areas of the photoresist and without significant outgassing or popping are provided by employing novel 1,2-diazonaphthoquinone-4- or -5-sulfonate esters of 2,3,4,3',4',5'-hexahydroxybenzophenone with a novel isomeric distribution of esters. The novel isomeric distribution of 1,2-diazonaphthoquinone-4- or -5-sulfonate esters of 2,3,4,3',4',5'-hexahydroxybenzophenone is characterized by two major isomers, together comprising at least about 70 % by weight of the photoactive compound, and wherein the least polar isomer comprises only about 40 %.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100306808-B1
priorityDate 1992-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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