http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05341514-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L21-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03F7-022
filingDate 1992-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4eb526dd1ede469835cc80c2e01abf2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82d2e7bd7d775c3e6365dd10d40840a1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e8c6788d846774f20e5ac920e2e11e3
publicationDate 1993-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05341514-A
titleOfInvention Positive photoresist composition
abstract (57) [Summary] [Structure] The positive photoresist composition of the present invention comprises a polyhydroxy compound represented by the following general formula (1): 2-naphthoquinonediazide-5- (and / or -4-) It contains a sulfonic acid ester and an alkali-soluble resin. [Chemical 1] In the formula, R represents a monovalent or divalent organic group. R 1 to R 4 May be the same or different and each represents a hydrogen atom, a hydroxyl group, a halogen atom, an alkyl group or an alkoxy group. n represents a number corresponding to a bond of the organic group R and is 1 or 2. [Effect] The positive photoresist containing the photosensitive material of the present invention is excellent in resolution, sensitivity, developability, and heat resistance, and is preferably used as a photoresist for microfabrication.
priorityDate 1992-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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