William G. Hatton, Nigel P. Hacker, et al.
Journal of the Chemical Society, Chemical Communications
Using photo-induced electron transfer technique, anion radicals of carboxylic acids (CH3)n(= 0,1,2,3)CH3-nCOOH and their ethyl esters were generated in argon matrices and examined by ESR. The study confirmed the previously reported photolysis path A for both the acid and ester anions, and revealed the presence of the second photolysis path B, an intramolecular abstraction. {A figure is presented} where R = ethyl or H. Both reaction paths are effected by visible light (λ =450 nm). Reaction path A prevailed for the ethyl ester anions, while reaction path B generally prevailed for the acid anions. For (CH3)3CCOOH anions, the intramolecular abstraction involving a γ proton was observed. The conformations (the pyramidal shape and the azimuthal position of the β alkyl group) and the unpaired electron distributions of the acid and ester anions given by the AM1-MNDO molecular orbital method are in excellent agreement with those deduced from the ESR spectra observed at 4 K. © 1994.
William G. Hatton, Nigel P. Hacker, et al.
Journal of the Chemical Society, Chemical Communications
Ralf Köppe, Paul H. Kasai
JACS
Paul M. Jones, Paul H. Kasai
Journal of Physical Chemistry
Paul H. Kasai, Vedantham Raman
Tribology Letters