The rearranged products in thermal decomposition of 2,5-diaryl-1,4-dithiin. Evidence for valence isomerization of 1,4-dithiin system.
β Scribed by Keiji Kobayashi; Kiyoshi Mutai; Hayao Kobayashi
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 246 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Bis(2,4-diaryl-3-thienyl) disulfide was isolated in the thermal decomposition of 2,5-diaryl-1,4-dithiin.
The formation of the rearranged product as well as the kinetic data suggest strongly the valence isomerization of 2,5-diaryl-1,4-dithiin in the course of the decomposition.
π SIMILAR VOLUMES
1,2,4,5-Tetra-l-butylbenzene (394) (TTBB) is believed to be a highly strained boat-shaped molecule (4) (I) and so might be expected to undergo photoisomerisation to a Dewar benzene (II) more readily than does 1,2,4-trit-butylbenzene(5'6), which was the first compound reported to undergo such a conve
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