Volume polarization in reaction field theory

被引:131
作者
Zhan, CG [1 ]
Bentley, J
Chipman, DM
机构
[1] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
D O I
10.1063/1.475371
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In continuum reaction field models of solvation, unconstrained quantum mechanical calculation of the solute electronic structure inevitably leads to penetration of some solute charge density outside the cavity and into the solvent dielectric region. This produces a rarely recognized or treated volume polarization that contributes in addition to the commonly considered surface polarization. In this work a new practical implementation is described for quantitatively evaluating both volume and surface polarization contributions to the solute-solvent interaction with an irregularly shaped cavity surface. For illustration, numerical results are presented on several representative small neutral, cation, and anion solutes. The volume polarization contributions to energies and dipole moments are found to be somewhat smaller than those from surface polarization, but not negligible. The results are also used to test several charge renormalization approaches that have been previously proposed in the literature. Compared to the exact volume polarization correction, these can sometimes lead to energy corrections of the wrong sign. A previously proposed method of simulating volume polarization through an additional surface polarization generally produces corrections of the right sign and of about the right magnitude. (C) 1998 American Institute of Physics.
引用
收藏
页码:177 / 192
页数:16
相关论文
共 38 条
[11]   SOLUTE-SOLVENT ELECTROSTATIC INTERACTIONS WITH NONHOMOGENEOUS RADIAL DIELECTRIC FUNCTIONS [J].
COSSI, M ;
MENNUCCI, B ;
TOMASI, J .
CHEMICAL PHYSICS LETTERS, 1994, 228 (1-3) :165-170
[12]  
Cramer C. S., 1996, SOLVENT EFFECTS CHEM, P1, DOI DOI 10.1007/0-306-46931-6_1
[13]  
Delley B, 1996, J COMPUT CHEM, V17, P1152, DOI 10.1002/(SICI)1096-987X(19960715)17:9<1152::AID-JCC7>3.0.CO
[14]  
2-R
[15]   ELECTRIC DIPOLE-MOMENTS OF LOW J STATES OF H2O AND D2O [J].
DYKE, TR ;
MUENTER, JS .
JOURNAL OF CHEMICAL PHYSICS, 1973, 59 (06) :3125-3127
[16]   Solvent effects .5. Influence of cavity shape, truncation of electrostatics, and electron correlation ab initio reaction field calculations [J].
Foresman, JB ;
Keith, TA ;
Wiberg, KB ;
Snoonian, J ;
Frisch, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (40) :16098-16104
[17]   SELF-CONSISTENT MOLECULAR-ORBITAL METHODS .25. SUPPLEMENTARY FUNCTIONS FOR GAUSSIAN-BASIS SETS [J].
FRISCH, MJ ;
POPLE, JA ;
BINKLEY, JS .
JOURNAL OF CHEMICAL PHYSICS, 1984, 80 (07) :3265-3269
[18]   INFLUENCE OF POLARIZATION FUNCTIONS ON MOLECULAR-ORBITAL HYDROGENATION ENERGIES [J].
HARIHARA.PC ;
POPLE, JA .
THEORETICA CHIMICA ACTA, 1973, 28 (03) :213-222
[19]  
JORTNER J, 1961, MOL PHYS, V24, P451
[20]   Theory of Solutions of Molecules Containing Widely Separated Charges with Special Application to Zwitterions [J].
Kirkwood, John G. .
JOURNAL OF CHEMICAL PHYSICS, 1934, 2 (07)