http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050049123-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F12-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L65-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L25-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-126
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G75-06
filingDate 2003-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7e2c4ccf2893f6cac8fddb247491116
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9253219a4bd05950e8a89b2fe487e1a6
publicationDate 2005-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20050049123-A
titleOfInvention Conductive polythiophene and method for preparing the same
abstract The conductive polythiophene of the present invention is characterized by using polyimidazolium styrene sulfonate represented by the following formula (1) as a dopant.n n n [Formula 1]n n n n n n n n Wherein R represents a linear or branched alkyl, alkoxy, hydroxy, acyl or amide functional group of C 1 -22 as a substituent in the o- or m- position of a sulfonate group; M is a pair of polystyrene sulfonates Ions represent imidazolium cations each substituted at the X, Y and Z positions; X, Y represent C 1 -22 linear or branched alkyl or substituted benzyl or substituted phenyl functional groups, respectively; Z is H or C 1 - 22 linear or side chain with an alkyl or substituted benzyl or phenyl substituted with functional groups of; n is 10-1000 Im).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100762014-B1
priorityDate 2003-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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