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On the structure of o-methylthiobenzoyloxy radical as revealed by CIDNP spectra and CNDO/2 MO calculations

✍ Scribed by Waro Nakanishi; Shōgo Koike; Makoto Inoue; Yoshitsugu Ikeda; Hiizu Iwamura; Yuzo Imahashi; Hiroshi Kihara; Masahiro Iwai


Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
244 KB
Volume
18
Category
Article
ISSN
0040-4039

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✦ Synopsis


Acceleration of a homolytic O-O bond cleavage by participation of a neighboring sulfur atom has been very clearly established in m-butyl o-methylthioperoxybenzoate (2) which decomposes ~a. lo4 times as fast as the parent peroxybensoate at 600~ in chlorobensene. The rate-determining step for the cleavage is described by the anchimerically assisted structure z. 2) CH3.S 0


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