Issue 7, 2003

Deprotonation yields, pKa, and aci-nitro decay rates in some substituted o-nitrobenzaldehydes

Abstract

In this paper we report the deprotonation yields, the pKa, and decay kinetics of the aci-nitro intermediates of some substituted 2-nitrobenzaldehydes that can be used as photoactivatable caged proton compounds. The decay of the aci-nitro absorbance for 2-nitrobenzaldehyde occurs within a few nanoseconds from photoexcitation. Addition of electron donating methoxy substituents at positions 4 and 5 leads to lower deprotonation yields, higher pKa, and slower decays of the aci-nitro intermediates. On the contrary, the decay rate is accelerated by the introduction of an electron-withdrawing Cl atom at position 4 in the phenyl ring, with little influence on the deprotonation yield and pKa of the aci-nitro intermediate.

Graphical abstract: Deprotonation yields, pKa, and aci-nitro decay rates in some substituted o-nitrobenzaldehydes

Article information

Article type
Paper
Submitted
17 Feb 2003
Accepted
14 Mar 2003
First published
09 Apr 2003

Photochem. Photobiol. Sci., 2003,2, 796-800

Deprotonation yields, pKa, and aci-nitro decay rates in some substituted o-nitrobenzaldehydes

S. Abbruzzetti, M. Carcelli, D. Rogolino and C. Viappiani, Photochem. Photobiol. Sci., 2003, 2, 796 DOI: 10.1039/B301818K

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