Issue 17, 2008

Novel photosystem involving protonation and deprotonation processes modelled on a PYP photocycle

Abstract

The synthesis of novel ortho-coumaric acid derivatives, with an amide group linked with an olefin moiety, which introduced photoinduced switching of the intramolecular hydrogen bonds is presented. An intramolecular OH⋯O[double bond, length as m-dash]C hydrogen bond formed in a Z-phenol compound was switched to an intramolecular NH⋯O hydrogen bond in Zphenolate state via deprotonation. The pKa value of the Z-phenol derivative was lower than that of E-phenol, and a novel photocycle system involving protonation and deprotonation processes was achieved.

Graphical abstract: Novel photosystem involving protonation and deprotonation processes modelled on a PYP photocycle

Supplementary files

Article information

Article type
Paper
Submitted
01 May 2008
Accepted
30 May 2008
First published
01 Jul 2008

Org. Biomol. Chem., 2008,6, 3118-3126

Novel photosystem involving protonation and deprotonation processes modelled on a PYP photocycle

T. Matsuhira, K. Tsuchihashi, H. Yamamoto, T. Okamura and N. Ueyama, Org. Biomol. Chem., 2008, 6, 3118 DOI: 10.1039/B807417H

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