Dimesitylcarbene: the distinct chemistries of its singlet and triplet states

AS Nazran, D Griller

Index: Nazran, Avtar S.; Griller, David Journal of the Chemical Society, Chemical Communications, 1983 , # 15 p. 850 - 851

Full Text: HTML

Citation Number: 0

Abstract

The singlet states of diarylcarbenes are thought to insert into the 0-H bonds of alcohols and to add stereospecifically to olefins. By contrast, their triplet ground states are thought to be efficient hydrogen abstracting agents and are believed to add non-stereospecifically to olefins.1-12 The experimental data supporting these hypotheses are equivocal. For example, optical absorption spectra due to the triplet states of diphenyl~arbene,~~~,~~ fluoreny1idene,'l*l2 and 1 - ...

Related Articles:

Polymethylated and poly (tert) butylated diphenylcarbenes. Generation, reactions, kinetics, and deuterium isotope effects of sterically congested triplet carbenes

[Tomioka, Hideo; Okada, Hidetsumu; Watanabe, Tetsuya; Banno, Kohji; Komatsu, Kazunori; Hirai, Katsuyuki Journal of the American Chemical Society, 1997 , vol. 119, # 7 p. 1582 - 1593]

Polymethylated and poly (tert) butylated diphenylcarbenes. Generation, reactions, kinetics, and deuterium isotope effects of sterically congested triplet carbenes

[Tomioka, Hideo; Okada, Hidetsumu; Watanabe, Tetsuya; Banno, Kohji; Komatsu, Kazunori; Hirai, Katsuyuki Journal of the American Chemical Society, 1997 , vol. 119, # 7 p. 1582 - 1593]

More Articles...