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