http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H083157-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D343-00
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filingDate 1994-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9123c3e3bfbb93ea30afe35274e57479
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eed147e31bf3b322165ab154d5bdb0aa
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publicationDate 1996-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H083157-A
titleOfInvention Benzotrichalcogenols, radical cation derivatives thereof, and methods for producing the same
abstract (57) [Summary] [Object] To provide benzotrichalcogenols containing sulfur and / or selenium, in which cyclic trichalcogenides are bonded to a benzene ring, which are suitable as EC materials. [Structure] Compound of the above formula 4,7-dimethoxy-1,2,3 -Benzotrithiol was synthesized. To this 2 mmol / l acetonitrile solution, tetrabutylammonium perchlorate was added to 0.1 mol / l to prepare a sample solution, and to this solution, glassy carbon was used as a working electrode, platinum was used as a counter electrode, and An Ag / AgNO 3 electrode was immersed as a reference electrode. From the obtained cyclic voltammogram, this substance shows a reversible oxidation / reduction process with potential scanning, The redox potential was 0.70 V vs Ag / AgNO 3 . Also, with the oxidation / reduction process, a reversible color change of the sample solution was observed, in which the neutral species became red and the radical cation species became purple.
priorityDate 1994-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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