http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100243491-B1

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filingDate 1996-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23a5ce805455d2776099d7a753b74684
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ddcc635330650d154e973d543cc4eba0
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publicationDate 2000-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100243491-B1
titleOfInvention New Sulfonium Salts and Chemically Amplified Forged Resist Materials
abstract The sulfonium salt which is represented by following General formula (1), has at least 1 acid labile group in a phenyl group in a molecule, and has a linear, branched or cyclic electron withdrawing group substituted alkyl or aryl sulfonate is provided. .n n n n n n n n Wherein each R 1 is the same or different and is an alkyl group, an alkoxy group or a dialkylamino group; OR 2 is an acid labile group; Y is a straight, branched or cyclic alkyl or aryl sulfo having 2 to 20 carbon atoms In the case of an alkyl group, in the case of an alkyl group, one or two or more of the hydrogen atoms bonded to the carbon atom after its β position are substituted with an electron withdrawing group such as fluorine and a nitro group, and in the case of an aryl group, one of the hydrogen atoms of the benzene ring is used. Or two or more are substituted with an electron withdrawing group such as fluorine, nitro group, n is an integer of 0 to 2, m is an integer of 1 to 3, n + m is 3, r is 1 or more and 5 or less P is an integer of 0-5, q is an integer of 0-4, q + r is an integer of 1-5).n n n The novel sulfonium salt of the general formula (1) according to the present invention can increase the dissolution contrast of the exposed portion and the unexposed portion, and furthermore, at the time of exposure, substituted alkyl which is a weak acid as compared to trifluoromethanesulfonic acid, which is a conventionally generated acid, and the like. Alternatively, since aryl sulfonic acid is generated, the effect of loss of activity due to side reactions or neutralization of the generated acid by basic compounds from the resist film surface in the PEB process after exposure can be reduced, and since it is not as weak as alkylsulfonic acid, it is relatively sensitive. It is good and effective as a component of a chemically amplified forged resist material having high resolution suitable for fine processing technology.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100986658-B1
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priorityDate 1995-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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