Theoretical study of ionization and one-electron oxidation potentials of N-heterocyclic compounds

Copyright © 2013 Wiley Periodicals, Inc.

Bibliographische Detailangaben
Veröffentlicht in:Journal of computational chemistry. - 1984. - 34(2013), 13 vom: 15. Mai, Seite 1094-100
1. Verfasser: Sviatenko, Liudmyla K (VerfasserIn)
Weitere Verfasser: Gorb, Leonid, Hill, Frances C, Leszczynski, Jerzy
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Journal of computational chemistry
Schlagworte:Journal Article Acetonitriles Heterocyclic Compounds Nitro Compounds Solvents acetonitrile Z072SB282N
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520 |a A number of density functionals was utilized to predict gas-phase adiabatic ionization potentials (IPs) for nitrogen-rich heterocyclic compounds. Various solvation models were applied to the calculation of difference in free energies of solvation of oxidized and reduced forms of heterocyclic compounds in acetonitrile (AN) for correct reproduction of their standard oxidation potentials. We developed generally applicable protocols that could successfully predict the gas-phase adiabatic ionization potentials of nitrogen-rich heterocyclic compounds and their standard oxidation potentials in AN. This approach is supported by a MPW1K/6-31+G(d) level of theory which uses SMD(UA0) approximation for estimation of solvation energy of neutral molecules and PCM(UA0) model for ionized ones. The mean absolute derivation (MAD) and root mean square error (RMSE) of the current theoretical models for IP are equal to 0.22 V and 0.26, respectively, and for oxidation potentials MAD = 0.13 V and RMSE = 0.17 
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650 7 |a Heterocyclic Compounds  |2 NLM 
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700 1 |a Gorb, Leonid  |e verfasserin  |4 aut 
700 1 |a Hill, Frances C  |e verfasserin  |4 aut 
700 1 |a Leszczynski, Jerzy  |e verfasserin  |4 aut 
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