http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09185093-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b8be6a6c990669567cc455d32b00535e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G02F1-3617
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-361
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-355
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-35
filingDate 1996-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2fdeea3ef2e656b475dafb3a56f147ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3a03c0b273b5f072f66d5c5e157c87c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1430baa8f1d600ad00e2984a06c28ee3
publicationDate 1997-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09185093-A
titleOfInvention Electro-optical device stable in the wavelength range of 600 to 1600 nanometers
abstract (57) Abstract: The present invention provides an electro-optical device comprising an NLO polymer in an active layer with improved stability for light in the wavelength range of 600-1600 nm guided through the electro-optical device. To do. The present invention relates to an electro-optical device comprising two cladding layers and an active layer sandwiched between the cladding layers, wherein the active layer is a nitrogen donor-delocalized. It comprises a non-linear optically active side chain polymer with an NLO chromophore with a π system-acceptor structure, the nitrogen donor not being directly attached to an alkyl group. NLO with nitrogen donor without adjacent linear alkyl groups There are two ways to create a chromophore. That is, the first method is to attach one or two aromatic groups. The nitrogen atom is further bound to the delocalized π system. If only one aromatic group is present, the nitrogen atom is In addition to the delocalized system, it is also bound to hydrogen or deuterium atoms. A second way to avoid adjacent alkyl groups is to employ a nitrogen donor moiety where no adjacent linear alkyl groups are present.
priorityDate 1995-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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