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Photochemical isomerizations of 2-phenyl-1,3-indanedione to E- and Z-benzalphthalide and of E-benzalphthalide to Z-benzalphthalide

Authors :
Anton Gáplovský
Jana Donovalová
Pavel Hrnčiar
Source :
Collection of Czechoslovak Chemical Communications. 49:1569-1576
Publication Year :
1984
Publisher :
Institute of Organic Chemistry & Biochemistry, 1984.

Abstract

The photochemical isomerizations have been studied of 2-phenyl-1,3-indanedione to mixture of E- and Z-benzalphthalide and of E-benzalphthalide to Z-benzalphthalide depending on the solvent used, concentration, and the light wavelength. The attempts at the reverse photochemical isomerization of E-benzalphthalide to 2-phenyl-1,3-indanedione have failed. Quantum yields of the isomerization of 2-phenyl-1,3-indanedione decrease in the following solvent series: cyclohexane acetonitrile benzene tetrachlormethane methanol. The isomerization quantum yield of 2-phenyl01,3-indanedione is inversely proportional to concentration of the starting substance, but the dependence of 1/φ on the concentration is not linear.

Details

ISSN :
12126950 and 00100765
Volume :
49
Database :
OpenAIRE
Journal :
Collection of Czechoslovak Chemical Communications
Accession number :
edsair.doi...........737f3c393b2db7b42d2c3f966695da8f
Full Text :
https://doi.org/10.1135/cccc19841569