http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1482013-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5ddadb999be4f451dfc44d8e359d8f6a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G11B7-248
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filingDate 2003-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56ae6ecc626dde61a055b11b4ee4d611
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36bb3cda7d6ffad439d18fdd46396beb
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_213c2a2ff64d127d5a4bf63d1a9c0ca6
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publicationDate 2007-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1482013-B1
titleOfInvention Phthalocyanine compound, process for producing the same, and optical recording medium containing the same
abstract A phthalocyanine compound (1) which is produced by reacting a phthalocyanine compound (3), which does not contain organometal residual groups, with a Wilsmyer complex and a compound having a constituent such as formanilide and then by reacting with ferrocene carboxylate amide and purifying it from the resulting mixture, is new. The phthalocyanine compound (1) is represented by formula (I); [Image] M : two hydrogen atoms, divalent metal atom, trivalent metal atom having one substituent, tetravalent metal having two substituents or oxymetal ; L 1>- L 4>groups represented by (a), (b) and (c); X : alkyl, alkoxy, alkylthio, aryloxy or arylthio group ; R : H, 1-6C alkyl, 6-10C aryl group ; A : carbonyl, thiocarbonyl, sulfone, sulfine or carboimide group ; Y : residue group of a metal compound ; Z : H atom, NO 2group or halogen atom At least one of L 1>- L 4>is (a) or (b). [Image].
priorityDate 2002-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 571.