Photoinduced electron transfer in aliphatic peptides
D Birch, JD Coyle, RR Hill, GE Jeffs
Index: Birch, David; Coyle, John D.; Hill, Roger R.; Jeffs, Graham E. Journal of the Chemical Society, Chemical Communications, 1986 , # 4 p. 293 - 295
Full Text: HTML
Citation Number: 3
Abstract
Product analysis in the photolysis of triglycine in neutral aqueous solution suggests that the initial intramolecular electron transfer from the carboxylate to the peptide group, shown to lead to efficient (ϕ 0.44±0.11) photodegradation for glycylglycine, may be followed by transfer to the second peptide group.
Related Articles:
[Mizushima et al. Journal of the American Chemical Society, 1951 , vol. 73, p. 1330,1331]
[Kuroda, Yasuhisa; Ueda, Hiroshi; Nozawa, Hiroshi; Ogoshi, Hisanobu Tetrahedron Letters, 1997 , vol. 38, # 45 p. 7901 - 7904]