http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107188853-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1044
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1007
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-6572
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
filingDate 2017-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107188853-B
titleOfInvention Tetrastyryl blue light material containing benzimidazole unit and preparation method and application
abstract The invention discloses a tetrastyryl blue light material containing benzimidazole units, as shown in structural formula I or II, wherein: R 1 is H, tert-butyl, n-butyl, and hydroxyl. R 2 is an alkyl group. First prepare 2-nitro-N-tert-butylphenylaniline or 2-nitro-N-n-butylaniline precursor and 4-aldehyde tetraphenylene precursor, and then obtain formula I or II through cyclization reaction compound. The preparation method of the compound is easy to operate, the reaction is mild and the yield is high, the compound has high decomposition temperature and glass transition temperature, and exhibits blue fluorescence and good monochromatic performance, and the OLED device prepared by using the compound as a light-emitting material has blue light. Emission, start-up voltage 3.3V, maximum brightness efficiency 1.48cd/A.
priorityDate 2017-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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