Azoporphyrin : the porphyrin analogue of azobenzene


Autoria(s): Esdaile, Louisa J.; Jensen, Paul; McMurtrie, John C.; Arnold, Dennis P.
Data(s)

01/02/2007

Resumo

Azobenzenes (1,2-diaryldiazenes) are very important organic pigments, and they have a unique place in the field of photoresponsive conjugated molecules due to their (usually) reversible E/Z photoisomerisation. The current intense interest in molecular analogues of mechanical components and information storage and processing elements has stimulated research into conjugated molecules whose shape and/or optical properties can be switched electro- or photochemically. Among the classes of conjugated pigments being explored in these contexts are the porphyrinoids, which offer advantages of intense light absorption, a variety of accessible oxidation states, and synthetic control of properties through peripheral or central substitution. Extension of porphyrinoid conjugation can be achieved by linking the peripheral carbons either by three direct bonds (as in the “porphyrin tapes” of Osuka et al.) or through potentially conjugating bridges such as alkenes or, even better, alkynes.

Formato

application/pdf

Identificador

http://eprints.qut.edu.au/40625/

Publicador

John Wiley & Sons

Relação

http://eprints.qut.edu.au/40625/1/c40625.pdf

DOI:10.1002/anie.200604658

Esdaile, Louisa J., Jensen, Paul, McMurtrie, John C., & Arnold, Dennis P. (2007) Azoporphyrin : the porphyrin analogue of azobenzene. Angewandte Chemie International Edition, 46(12), pp. 2090-2093.

Direitos

Copyright 2007 John Wiley & Sons

Fonte

Chemistry; Faculty of Science and Technology

Palavras-Chave #030503 Organic Chemical Synthesis #porphyrinoids #azo compounds #crystal structure #copper-catalysed coupling #absorption spectroscopy
Tipo

Journal Article