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Issue 28, 2011
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Control of electron-transfer reduction by protonation of zinc octabutoxyphthalocyanine assisted by intramolecular hydrogen bonding

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Abstract

Facile protonation of α-octabutoxyphthalocyaninato zinc(II) (Zn(OBu)8Pc) occurs to afford up to tetra-protonated species stabilized by intramolecular hydrogen bonding, resulting in positive shifts of the reduction potentials of Zn(OBu)8PcHnn+ (n = 1–4) with increasing the number of protons attached to facilitate electron-transfer reduction.

Graphical abstract: Control of electron-transfer reduction by protonation of zinc octabutoxyphthalocyanine assisted by intramolecular hydrogen bonding

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Supplementary files

Article information


Submitted
09 May 2011
Accepted
01 Jun 2011
First published
17 Jun 2011

Chem. Commun., 2011,47, 7986-7988
Article type
Communication

Control of electron-transfer reduction by protonation of zinc octabutoxyphthalocyanine assisted by intramolecular hydrogen bonding

T. Honda, T. Kojima and S. Fukuzumi, Chem. Commun., 2011, 47, 7986 DOI: 10.1039/C1CC12710A

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