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Real space electrostatics for multipoles. III. Dielectric properties.
Lamichhane, Madan; Parsons, Thomas; Newman, Kathie E; Gezelter, J Daniel.
Afiliação
  • Lamichhane M; Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556, USA.
  • Parsons T; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, USA.
  • Newman KE; Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556, USA.
  • Gezelter JD; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, USA.
J Chem Phys ; 145(7): 074108, 2016 Aug 21.
Article em En | MEDLINE | ID: mdl-27544088
ABSTRACT
In Papers I and II, we developed new shifted potential, gradient shifted force, and Taylor shifted force real-space methods for multipole interactions in condensed phase simulations. Here, we discuss the dielectric properties of fluids that emerge from simulations using these methods. Most electrostatic methods (including the Ewald sum) require correction to the conducting boundary fluctuation formula for the static dielectric constants, and we discuss the derivation of these corrections for the new real space methods. For quadrupolar fluids, the analogous material property is the quadrupolar susceptibility. As in the dipolar case, the fluctuation formula for the quadrupolar susceptibility has corrections that depend on the electrostatic method being utilized. One of the most important effects measured by both the static dielectric and quadrupolar susceptibility is the ability to screen charges embedded in the fluid. We use potentials of mean force between solvated ions to discuss how geometric factors can lead to distance-dependent screening in both quadrupolar and dipolar fluids.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos