http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015107936-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J9-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J183-08
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filingDate 2013-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae1d1600acfa5e1c42cab47cac2efe0e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb2415c1fdcfe3e6afb40e962892206e
publicationDate 2015-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2015107936-A
titleOfInvention Process for producing glycidyl isocyanuryl-modified polysiloxane
abstract When manufacturing a light-emitting device by flip-chip mounting a light-emitting element such as a light-emitting diode (LED) element on a wiring board using an anisotropic conductive adhesive, it is practically not discolored by heat or light. A siloxane compound useful as a curable compound constituting an insulating resin component of an anisotropic conductive adhesive exhibiting sufficient die shear strength can be produced. An epoxy group-containing isocyanuryl-modified polysiloxane, which is a thermosetting compound suitable for a light-reflective anisotropic conductive adhesive, contains a hydrogen polysiloxane and an epoxy group having a terminal unsaturated alkenyl group. The isocyanurate is subjected to a hydrosilylation reaction in the presence of 20 ppm or less of a platinum catalyst. [Selection] Figure 2
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