Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_76baf08afb64a9d094cd03eb107f7124 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2800-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2810-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F4-65912 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F4-65908 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F4-65927 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G81-021 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F10-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F10-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F8-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F8-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F10-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F10-02 |
filingDate |
2013-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58f8cd630c5b1e3541fba23ae1187bc4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ad99a52fa2a6635a1479effbf6c6173 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_618865560f9d015838c8b83d076bba3b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9febe64cb629c4790f26c919e33c7773 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef69d266871130bc45c8a02f92437f55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_900369962ab0d92b97cb4765c80bb3d3 |
publicationDate |
2014-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-2014088262-A1 |
titleOfInvention |
Friedel Crafts Alkylation of Aromatics Using Vinyl Terminated Macromonomers |
abstract |
This invention relates to a polyolefin comprising one or more aromatic moieties according to the following formulae: n n n n n n n n n n wherein the PO is the residual portion of a vinyl terminated macromonomer (VTM) having had a terminal unsaturated carbon of an allylic chain and a vinyl carbon adjacent to the terminal unsaturated carbon;n nAr is attached to the terminal portion of the VTM to provide PO—Ar or at the vinylidene carbon of the VTM to provide PO—CH(Ar)CH 3 ; andn nAr is a substituted or unsubstituted aromatic group. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2016257841-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10590309-B2 |
priorityDate |
2012-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |