http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006173216-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K50-14
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K50-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C211-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-633
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-58
filingDate 2004-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_926ee42e85bb6db8507ea8e27c4721e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03f88e2c587bc67dcae3a52d8bd7c3fd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_801879ef2cad3494221dc35ccb27c511
publicationDate 2006-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2006173216-A1
titleOfInvention Novel 1, 3, 5 tris (arylamino) benzenes
abstract The invention provides 1,3,5-tris(arylamino)benzenes represented by the general formula (I) n nwherein A is naphthyl, anthryl or phenanthryl group, and R is hydrogen atom or diarylamino group. These 1,3,5-tris(arylamino)benzenes have oxidation potentials in the range of about 0.5-0.6V, excellent reversibility in oxidation-reduction process, high glass transition temperatures and high heat resistance, so that they can form practicable organic semiconductor film readily by a coating method or a vacuum deposition method. In addition, they are capable of forming stable and durable amorphous film useful as high performance organic semiconductors at normal temperatures or higher with no aid of binder resins, that is, by themselves.
priorityDate 2003-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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