Abstract
(Figure Presented) One way only: The Z → E photoisomerization of stilbene under visible light occurs within a porous coordination network (see picture). The reaction proceeds through the photoexcitation of a chargetransfer complex between the highly elec-tron-deficient ligand and the stilbene in the pore. The in situ formed E isomer rapidly exchanges with unreacted Z isomer in solution, hence a catalytic amount of the network is sufficient to promote the reaction. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Ohara, K., Inokuma, Y., & Fujita, M. (2010). The catalytic Z to E isomerization of stilbenes in a photosensitizing porous coordination network. Angewandte Chemie - International Edition, 49(32), 5507–5509. https://doi.org/10.1002/anie.201001902
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