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Kemp Elimination Reaction Catalyzed by Electric Fields.

Authors :
Acosta-Silva C
Bertran J
Branchadell V
Oliva A
Source :
Chemphyschem : a European journal of chemical physics and physical chemistry [Chemphyschem] 2020 Feb 17; Vol. 21 (4), pp. 295-306. Date of Electronic Publication: 2020 Jan 17.
Publication Year :
2020

Abstract

The Kemp elimination reaction is the most widely used in the de novo design of new enzymes. The effect of two different kinds of electric fields in the reactions of acetate as a base with benzisoxazole and 5-nitrobenzisoxazole as substrates have been theoretically studied. The effect of the solvent reaction field has been calculated using the SMD continuum model for several solvents; we have shown that solvents inhibit both reactions, the decrease of the reaction rate being larger as far as the dielectric constant is increased. The diminution of the reaction rate is especially remarkable between aprotic organic solvents and protic solvents as water, the electrostatic term of the hydrogen bonds being the main factor for the large inhibitory effect of water. The presence of an external electric field oriented in the direction of the charge transfer (z axis) increases it and, so, the reaction rate. In the reaction of the nitro compound, if the electric field is oriented in an orthogonal direction (x axis) the charge transfer to the NO <subscript>2</subscript> group is favored and there is a subsequent increase of the reaction rate. However, this increase is smaller than the one produced by the field in the z axis. It is worthwhile mentioning that one of the main effects of external electric fields of intermediate intensity is the reorientation of the reactants. Finally, the implications of our results in the de novo design of enzymes are discussed.<br /> (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1439-7641
Volume :
21
Issue :
4
Database :
MEDLINE
Journal :
Chemphyschem : a European journal of chemical physics and physical chemistry
Publication Type :
Academic Journal
Accession number :
31840917
Full Text :
https://doi.org/10.1002/cphc.201901155