Journal of the American Chemical Society

Mechanisms for the photooxidation of protoporphyrin IX in solution

GS Cox, DG Whitten

Index: Cox, G. Sidney; Whitten, David G. Journal of the American Chemical Society, 1982 , vol. 104, # 2 p. 516 - 521

Full Text: HTML

Citation Number: 79

Abstract

Abstract: Protoporphyrin IX dimethyl ester (la) is photooxidized upon irradiation in aprotic organic solvents in the presence of oxygen to yield a mixture of hydroxyaldehydes (2 and 3)( photoprotoporphyrins), monoformylmonovinyldeuteroporphyrins (4 and 5). and diformyldeuteroporphyrin (6). Studies of the reaction under a variety of conditions show that the major portion of all of these products arises via a singlet oxygen path. The formyl ...

Related Articles:

Improved methods for the synthesis of porphyrin alcohols and aldehydes from protoporphyrin IX dimethyl ester and their further modification

[Kahl, Stephen B.; Schaeck, John J.; Koo, Myoung-Seo Journal of Organic Chemistry, 1997 , vol. 62, # 6 p. 1875 - 1880]

Improved methods for the synthesis of porphyrin alcohols and aldehydes from protoporphyrin IX dimethyl ester and their further modification

[Kahl, Stephen B.; Schaeck, John J.; Koo, Myoung-Seo Journal of Organic Chemistry, 1997 , vol. 62, # 6 p. 1875 - 1880]

More Articles...