Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_255ea743d5f234e70fb6a537572bcaa2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f1bf4e500f04853ff797a782e048b1c7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_524061d80ca2efbd5d47b0506b874c9a |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-322 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1029 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1059 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01G9-2059 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K9-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B57-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B23-166 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-022 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B23-105 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B55-005 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B69-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02 |
filingDate |
2014-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0274224c7cfb1be8ff334b0a67201c03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4dfd7e11d07e3a57a272cfc50fef6e8 |
publicationDate |
2015-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
WO-2015077427-A1 |
titleOfInvention |
Highly Fluorescent Pyrrole-BF2 Chromophores |
abstract |
Fluorescent chromophores nicknamed BOPHY are provided. The chromophores may be readily synthesized in two steps from readily available reagents via the coupling of a pyrrole aldehyde or ketone with hydrazine, followed by reaction with BF 3 . The resultant symmetric and dimeric tetracycle is comprised of two BF 2 units in six-member chelate rings, appended by pyrrole units on the periphery. The quantum yield of fluorescence for the unmodified compound and the tetramethyl variant are near unity, with values 95 and 92% respectively in CH 2 Cl 2 . |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022233795-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10676489-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2684052-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9273078-B2 |
priorityDate |
2013-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |