Reactivity toward Dioxygen of Dicobalt Face-to-Face Diporphyrins in Aprotic Media. Experimental and Theoretical Aspects. Possible Mechanistic Implication in the Reduction of Dioxygen-Reference-Cited by-同舟云学术

Reactivity toward Dioxygen of Dicobalt Face-to-Face Diporphyrins in Aprotic Media. Experimental and Theoretical Aspects. Possible Mechanistic Implication in the Reduction of Dioxygen

Published:1997-07-01 Issue:26 Volume:119 Page:6095-6106
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Le Mest Yves¹,Inisan Claude¹,Laouénan André¹,L'Her Maurice¹,Talarmin Jean¹,El Khalifa Moulay¹,Saillard Jean-Yves¹

Affiliation:

1. Contribution from the Laboratoire de Chimie, Electrochimie Moléculaires et Chimie Analytique, UMR CNRS 6521, Université de Bretagne Occidentale, B.P. 809, 29285 Brest Cedex, France, and Laboratoire de Chimie du Solide et Inorganique Moléculaire, UMR CNRS 6511, Université de Rennes 1, 35042 Rennes Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9618659

Reference97 articles.

1. Molecular Catalysts for Multielectron Redox Reactions of Small Molecules: The“Cofacial Metallodiporphyrin” Approach

2. Potent catalysis of the electroreduction of oxygen to water by dicobalt porphyrin dimers adsorbed on graphite electrodes

3. Electrode catalysis of the four-electron reduction of oxygen to water by dicobalt face-to-face porphyrins

4. (c) Collman, J. P.; Anson, F. C.; Bencosme, S.; Chong, A.; Collins, T.; Denisevich, P.; Evitt, E.; Geiger, T.; Ibers, J.; Jameson, G.; Konai, Y.; Koval, C.; Meier, K.; Oakley, R.; Pettman, R.; Schmittou, E.; Sessler, J. InOrganic Synthesis, Today and Tomorrow; Trost, B. M., Hutchinson, C. R., Eds.; Pergamon Press: New York, 1981; pp 29−45.

5. Dependence of electrocatalysis for oxygen reduction by adsorbed dicobalt cofacial porphyrins upon catalyst structure

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