Issue 42, 2010

Effect of anion binding on charge stabilization in a bis-fullerene–oxoporphyrinogen conjugate

Abstract

Presence of strongly binding anion, F stabilizes the photo-induced charge-separated states of a bis-fullerene-substituted oxoporphyrinogen due to the large shift in the oxidation potential of the oxoporphyrinogen moiety upon anion binding through hydrogen bonding at its core.

Graphical abstract: Effect of anion binding on charge stabilization in a bis-fullerene–oxoporphyrinogen conjugate

Supplementary files

Article information

Article type
Communication
Submitted
10 Aug 2010
Accepted
06 Sep 2010
First published
22 Sep 2010

Chem. Commun., 2010,46, 7933-7935

Effect of anion binding on charge stabilization in a bis-fullereneoxoporphyrinogen conjugate

J. P. Hill, M. E. El-Khouly, R. Charvet, N. K. Subbaiyan, K. Ariga, S. Fukuzumi and F. D'Souza, Chem. Commun., 2010, 46, 7933 DOI: 10.1039/C0CC03167D

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