An interpretation of the enhancement of the water dipole moment due to the presence of other water molecules

被引:91
作者
Kemp, Daniel A. [1 ]
Gordon, Mark S. [1 ]
机构
[1] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
关键词
D O I
10.1021/jp801921f
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
The dipole moment of the gas phase water monomer is 1.85 D. When solvated in bulk water, the dipole moment of an individual water molecule is observed to be enhanced to the much larger value of 2.9 +/- 0.6 D. To understand the origin of this dipole moment enhancement, the effective fragment potential (EFP) method is used to solvate an ab initio water molecule to predict the dipole moments for various cluster sizes. The dipole moment as a function of cluster size, nH(2)O, is investigated [for n = 6-20 (even n), 26, 32, 41, and 50]. Localized charge distributions are used in conjunction with localized molecular orbitals to interpret the dipole moment enhancement. These calculations suggest that the enhancement of the dipole moment originates from the decrease of the angle between the dipole vectors of the lone pairs on oxygen as the number of hydrogen bonds to that oxygen increases. Thus, the decreased angle, and the consequent increase in water dipole moment, is most likely to occur in environments with a larger number of hydrogen bonds, such as the center of a cluster of water molecules.
引用
收藏
页码:4885 / 4894
页数:10
相关论文
共 79 条
[1]   Solvent effects on the SN2 reaction:: Application of the density functional theory-based effective fragment potential method [J].
Adamovic, I ;
Gordon, MS .
JOURNAL OF PHYSICAL CHEMISTRY A, 2005, 109 (08) :1629-1636
[2]   Density functional theory based effective fragment potential method [J].
Adamovic, I ;
Freitag, MA ;
Gordon, MS .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (15) :6725-6732
[3]   A MOLECULAR-DYNAMICS STUDY OF POLARIZABLE WATER [J].
AHLSTROM, P ;
WALLQVIST, A ;
ENGSTROM, S ;
JONSSON, B .
MOLECULAR PHYSICS, 1989, 68 (03) :563-581
[4]   A derivation of the frozen-orbital unrestricted open-shell and restricted closed-shell second-order perturbation theory analytic gradient expressions [J].
Aikens, CM ;
Webb, SP ;
Bell, RL ;
Fletcher, GD ;
Schmidt, MW ;
Gordon, MS .
THEORETICAL CHEMISTRY ACCOUNTS, 2003, 110 (04) :233-253
[5]   QUANTUM-THEORY OF ATOMS IN MOLECULES - DALTON REVISITED [J].
BADER, RFW ;
NGUYENDANG, TT .
ADVANCES IN QUANTUM CHEMISTRY, 1981, 14 :63-124
[6]   Electron distribution in water [J].
Badyal, YS ;
Saboungi, ML ;
Price, DL ;
Shastri, SD ;
Haeffner, DR ;
Soper, AK .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (21) :9206-9208
[7]   COOPERATIVE EFFECTS IN SIMULATED WATER [J].
BARNES, P ;
FINNEY, JL ;
NICHOLAS, JD ;
QUINN, JE .
NATURE, 1979, 282 (5738) :459-464
[8]   Molecular multipole moments of water molecules in ice Ih [J].
Batista, ER ;
Xantheas, SS ;
Jónsson, H .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (11) :4546-4551
[9]   Multipole moments of water molecules in clusters and ice Ih from first principles calculations [J].
Batista, ER ;
Xantheas, SS ;
Jónsson, H .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (13) :6011-6015
[10]   Electric fields in ice and near water clusters [J].
Batista, ER ;
Xantheas, SS ;
Jónsson, H .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (07) :3285-3292