Photophysical features of naphthols having esters, formyl and acetyl groups and the difluoroboronated complex in solution and the solid state-Reference-Cited by-同舟云学术

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Photophysical features of naphthols having esters, formyl and acetyl groups and the difluoroboronated complex in solution and the solid state

Published:2018-06 Issue: Volume:360 Page:204-209
ISSN:1010-6030
Container-title:Journal of Photochemistry and Photobiology A: Chemistry
language:en
Short-container-title:Journal of Photochemistry and Photobiology A: Chemistry

Author:

Yamaji Minoru,Okamoto Hideki

Funder

Grant-in-Aid for Scientific Research

Science & Technology, Gunma University

Publisher

Elsevier BV

Subject

General Physics and Astronomy,General Chemical Engineering,General Chemistry

Reference50 articles.

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2. Proton transfer in solid 1-phenylbutane-1,3-dione and related 1,3-diones as studied by carbon-13 CPMAS NMR spectroscopy and AM1 calculations;Vila;J. Phys. Chem.,1991

3. Tautomeric equilibria in relation to p-electron delocalization;Raczynska;Chem. Rev.,2005

4. Photoketonization and excited state relaxation of dibenzoylmethane in non-polar solvents;Yankov;J. Photochem. Photobiol. A: Chem.,1988

5. Recovery mechanism of the reaction intermediate produced by photoinduced cleavage of the intramolecular hydrogen bond of dibenzoylmethane;Tobita;J. Photochem. Photobiol. A: Chem,1995

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