http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-3007234-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_52b2b51797a166092b209a654503858e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01S3-213
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01S3-213
filingDate 1980-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54f1d1c6a55f595934bcf4cf36a21537
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0dd647d42b0e96cdc883a98232afa128
publicationDate 1981-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-3007234-A1
titleOfInvention SUBSTITUTED P-TERPHENYLE AS STIMULATABLE MEDIA IN DYE LASERS
abstract New excitable media for dyestuff lasers contain (a new series of) substd. p-terphenyl dyestuffs of formula (I). In (I) R1, R2 and R3 are substitis. causing a shortwave shift of the fluorescence and absorption bands due to their electronic effects, e.g. CF3 or F, or twisting of the outer benzene rings due to their spatial size and thus a shortwave shift of the fluorescence and absorption bands, e.g. alkyl, CF3 or F gps. in the 2,6,2',3', 5',2" and 6" positions. (I) are present in an inert solvent (II). Pref. (I) is (A) 2,2"- or (B) 3,3"-bistrifluoromethyl-, (C) 2- methyl-, (D) 2-trifluoromethyl- or (E) 2,2"-dimethyl-p-terphenyl.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-3408028-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4876029-A
priorityDate 1980-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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