http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9850339-B2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c389d310f52125a947b3408cb0cf3283 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-3206 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-3215 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-4812 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-7621 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-4829 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-4825 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K19-3885 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G18-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G18-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-38 |
filingDate | 2014-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2017-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49b1a1d2c388eaff0b7fa4b7ca19f5c7 |
publicationDate | 2017-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-9850339-B2 |
titleOfInvention | Liquid crystalline polyurethane elastomer and method for producing same |
abstract | A liquid crystalline polyurethane elastomer is produced by reacting an isocyanate component, a high-molecular-weight polyol component and a mesogenic diol represented by formula (1), and having a crosslinking site that is introduced by a tri-functional or higher isocyanate in the isocyanate component and/or a high-molecular-weight polyol having a number average molecular weight of 400 or more and less than 7000 and having three or more hydroxy groups, in the high-molecular-weight polyol component, wherein the melting point of a mesogenic unit does not exist in a temperature range lying between the glass transition temperature (Tg) and the (liquid crystal phase)-to-(isotropic phase) transition temperature (Ti) of the polyurethane elastomer, and a liquid crystal is developed at a temperature between the Tg and the Ti. (In the formula, X represents an alkylene group having 3 to 20 carbon atoms; and Y represents a single bond, —N═N—, —CO—, —CO—O— or —CH═N—). |
priorityDate | 2013-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 192.