| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e0b5ef5f9f09be00bc585bd5999f4e95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e64e1b79ae46f56629fbb7bd594be9e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3b5262ecfe09a326bcf947f20154607d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e6b02f0e20553a792b3dc4ac9393671d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_faf522b8b83eded745c73018576219ba |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1416
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1433 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-027
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-50 |
| filingDate |
2007-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64eb11c0ce2dc6657e08d42b3c1b8064
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa41e669b82167f6db947434bfa3866b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b4ff29a3cdbf9966bb959c7fd14737a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d3fec789d6101676f5e2e085a05be31 |
| publicationDate |
2008-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2008010532-A1 |
| titleOfInvention |
Compound or salt thereof, processes for producing these, aromatic azo compounds, and fluorescent material |
| abstract |
A series of aromatic azo compounds (azoarene derivatives) was found to have a high fluorescence quantum yield. In particular, [2-(4-methoxyphenylazo)phenyl]bis(pentafluorophenyl)borane, which is an azobenzene derivative, had a fluorescence quantum yield in a room-temperature solution of 0.76, which was the highest in history. Various investigations on azobenzene derivatives have been made and many synthesis techniques have been established. A fluorescent material is provided which is useful because it has the intact advantage of the variety and simplicity of azobenzene derivative synthesis methods and because of the ease of regulating fluorescence wavelengths, etc. The compounds have excellent properties and are hence expected to be used in various applications. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111398468-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10495896-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112796007-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014202957-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111398468-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10175552-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9784980-B2 |
| priorityDate |
2006-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |