Literature DB >> 29572692

An extension of the Marcus equation: the Marcus potential energy function.

Soledad Gutiérrez-Oliva1, Bárbara Herrera1, Alejandro Toro-Labbé2.   

Abstract

An analytic potential function consistent with the Marcus equation for activation energy is formulated and used to reveal new insights into the activation process in chemical reactions. As for the Marcus equation, the new potential function depends only on two parameters, the reaction energy and the activation energy (or the so-called Marcus intrinsic activation energy). Combination of the Marcus potential with the reaction force analysis provides two-parameter analytic expressions for the reaction force, reaction force constant, and reaction works. Moreover, since the parameters necessary to define the Marcus potential energy function can be obtained experimentally, the present model may produce experimental analytic potentials allowing for new and interesting applications, thus emerging as a powerful tool to characterize activation processes in chemical reactions.

Keywords:  Activation energy; Marcus equation; Marcus potential energy; Reaction force; Reaction works

Year:  2018        PMID: 29572692     DOI: 10.1007/s00894-018-3633-8

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


  12 in total

1.  Accurate reaction paths using a Hessian based predictor-corrector integrator.

Authors:  Hrant P Hratchian; H Bernhard Schlegel
Journal:  J Chem Phys       Date:  2004-06-01       Impact factor: 3.488

2.  The role of the reaction force to characterize local specific interactions that activate the intramolecular proton transfers in DNA basis.

Authors:  Bárbara Herrera; Alejandro Toro-Labbe
Journal:  J Chem Phys       Date:  2004-10-15       Impact factor: 3.488

3.  Fine structure in the transition region: reaction force analyses of water-assisted proton transfers.

Authors:  Diana Yepes; Jane S Murray; Juan C Santos; Alejandro Toro-Labbé; Peter Politzer; Pablo Jaque
Journal:  J Mol Model       Date:  2012-06-26       Impact factor: 1.810

4.  The role of reaction force and chemical potential in characterizing the mechanism of double proton transfer in the adenine-uracil complex.

Authors:  Bárbara Herrera; Alejandro Toro-Labbé
Journal:  J Phys Chem A       Date:  2007-06-13       Impact factor: 2.781

5.  The reaction force and the transition region of a reaction.

Authors:  Alejandro Toro-Labbé; Soledad Gutiérrez-Oliva; Jane S Murray; Peter Politzer
Journal:  J Mol Model       Date:  2008-12-16       Impact factor: 1.810

6.  A detailed analysis of the mechanism of a carbocationic triple shift rearrangement.

Authors:  Daniela E Ortega; Soledad Gutiérrez-Oliva; Dean J Tantillo; Alejandro Toro-Labbé
Journal:  Phys Chem Chem Phys       Date:  2015-04-21       Impact factor: 3.676

7.  Study of antiradical mechanisms with dihydroxybenzenes using reaction force and reaction electronic flux.

Authors:  Cristina Ortega-Moo; Rocio Durán; Bárbara Herrera; Soledad Gutiérrez-Oliva; Alejandro Toro-Labbé; Rubicelia Vargas
Journal:  Phys Chem Chem Phys       Date:  2017-06-07       Impact factor: 3.676

8.  The mechanism of methanol decomposition by CuO. A theoretical study based on the reaction force and reaction electronic flux analysis.

Authors:  Maria Luisa Cerón; Barbara Herrera; Paulo Araya; Francisco Gracia; Alejandro Toro-Labbé
Journal:  J Mol Model       Date:  2010-10-19       Impact factor: 1.810

9.  Reaction force analysis of the effect of Mg(II) on the 1,3 intramolecular hydrogen transfer in thymine.

Authors:  Elizabeth Rincón; Pablo Jaque; Alejandro Toro-Labbé
Journal:  J Phys Chem A       Date:  2006-08-03       Impact factor: 2.781

10.  The catalytic effect of the NH3 base on the chemical events in the caryolene-forming carbocation cascade.

Authors:  Daniela E Ortega; Quynh Nhu N Nguyen; Dean J Tantillo; Alejandro Toro-Labbé
Journal:  J Comput Chem       Date:  2016-02-02       Impact factor: 3.376

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