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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S428-917
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02B20-30
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K50-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K50-17
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
filingDate 2007-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2014-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101356379-B1
titleOfInvention Capture Agents for Top Emission Organic Electroluminescent Devices and Top Emission Organic Electroluminescent Devices
abstract The present invention provides a capturing agent for a top emission type organic EL device that is easy to handle, has excellent optical characteristics, and has high capturing ability of water and oxygen.n n n The capture agent for a top emission type organic EL device consists of a compound represented by a following formula.n n n R 1 R 2 R 3 M... (One)n n n [Wherein R 1 , R 2 and R 3 are each one selected from the group consisting of hydrogen atom, alkyl group, alkenyl group, alkynyl group, cyclic alkyl group, aryl group, alkoxy group, carboxyl group, thiolate group and secondary amino group Of course, they are equal to each other or dollars, but are selected to have one or more MC bonds as a complement. M is aluminum or boron.]
priorityDate 2006-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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