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Issue 22, 2011
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Ultrafast irreversible phototautomerization of o-nitrobenzaldehyde

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Abstract

o-Nitrobenzaldehyde is photolabile because of an irreversible phototautomerization, whereas comparable aromatic compounds function as photoprotectors because the tautomerization is reversible. In this experimental and theoretical study we track down the cause of this difference to the electronic changes that occur during the tautomerization.

Graphical abstract: Ultrafast irreversible phototautomerization of o-nitrobenzaldehyde

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Publication details

The article was received on 23 Feb 2011, accepted on 11 Apr 2011 and first published on 06 May 2011


Article type: Communication
DOI: 10.1039/C1CC11085C
Citation: Chem. Commun., 2011,47, 6383-6385
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    Ultrafast irreversible phototautomerization of o-nitrobenzaldehyde

    A. Migani, V. Leyva, F. Feixas, T. Schmierer, P. Gilch, I. Corral, L. González and L. Blancafort, Chem. Commun., 2011, 47, 6383
    DOI: 10.1039/C1CC11085C

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