Coupled Electron-Proton Transfer in Interactions of Triplet C60 with Hydrogen-Bonded Phenols: Effects of Solvation, Deuteration, and Redox Potentials
- 1 December 1997
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (51) , 12601-12609
- https://doi.org/10.1021/ja9727528
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Reduction of Triplet C60by Hydrogen-Bonded Naphthols: Concerted Electron and Proton MovementFullerene Science and Technology, 1997
- C60 as a Photocatalyst of Electron-Transfer Processes: Reactions of Triplet C60 with Chloranil, Perylene, and Tritolylamine Studied by Flash Photolysis and FT-EPRThe Journal of Physical Chemistry, 1996
- Electroreduction of Buckminsterfullerene, C60, in aprotic solvents. Solvent, supporting electrolyte, and temperature effectsThe Journal of Physical Chemistry, 1992
- External heavy atom induced phosphorescence emission of fullerenes: the energy of triplet C60The Journal of Physical Chemistry, 1992
- Photoinduced charge transfer between fullerenes (C60 and C70) and semiconductor zinc oxide colloidsJournal of the American Chemical Society, 1991
- Oxidation of 10-methylacridan, a synthetic analog of NADH and deprotonation of its cation radical: convergent application of laser flash photolysis, and direct and redox catalyzed electrochemistry to the kinetics of deprotonation of the cation radicalThe Journal of Physical Chemistry, 1991
- The Relative Ease of Oxidation of Phenols and Phenolic Ethers. A Comparison of Reversible Redox Potentials.Acta Chemica Scandinavica, 1976
- Hydrogen bonding. VI. Dramatic difference between proton transfer and hydrogen bondingJournal of the American Chemical Society, 1971
- The hydroquinone–quinone redox behaviour in acetonitrileJournal of the Chemical Society D: Chemical Communications, 1969
- Propriétés physico-chimiques de composés à caractère aromatique—V: Etude, par spectroscopie ultraviolette, de l'interaction entre les dérivés monoazaaromatiques et les acides carboxyliques. Mise en évidence d'un potentiel à deux minimums pour le lien hydrogèneSpectrochimica Acta, 1963