Silicon−Carbon Unsaturated Compounds. 57. Photolysis of meso- and racemic-1,2-Diethyl-1,2-dimethyldiphenyldisilane, Direct Evidence for a Concerted 1,3-Silyl Shift to ortho-Carbon in the Phenyl Ring-Reference-Cited by-同舟云学术

Silicon−Carbon Unsaturated Compounds. 57. Photolysis of meso- and racemic-1,2-Diethyl-1,2-dimethyldiphenyldisilane, Direct Evidence for a Concerted 1,3-Silyl Shift to ortho-Carbon in the Phenyl Ring

Published:1996-01-01 Issue:29 Volume:118 Page:6853-6859
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ohshita Joji¹,Niwa Hiroyuki¹,Ishikawa Mitsuo¹,Yamabe Tokio¹,Yoshii Takao¹,Nakamura Kouichi¹

Affiliation:

1. Contribution from the Department of Applied Chemistry, Faculty of Engineering, Hiroshima University, Higashi-Hiroshima 724, Japan, and Department of Molecular Engineering, Faculty of Engineering, Kyoto University, Kyoto 606-01, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja960458u

Reference23 articles.

1. Photolysis of organopolysilanes. Novel addition reaction of aryl substituted disilanes to olefins

2. Photochemically generated silicon—carbon double-bonded intermediates

3. Photochemistry of Organopolysilanes

4. Photochemistry of 1,2-di-tert-butyl-1,1,2,2-tetraphenyldisilane, a clean, direct source of arylalkylsilyl radicals

5. Reactive intermediates from the photolysis of methylpentaphenyl- and pentamethylphenyldisilane

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