Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, Arkansas 72701, USA.
J Chem Phys. 2017 Oct 28;147(16):161726. doi: 10.1063/1.5001254.
An atomic version of the Millikan oil drop experiment is performed computationally. It is shown that for planar molecules, the atomic version of the Millikan experiment can be used to define an atomic partial charge that is free from charge flow contributions. We refer to this charge as the Millikan-Thomson (MT) charge. Since the MT charge is directly proportional to the atomic forces under a uniform electric field, it is the most relevant charge for force field developments. The MT charge shows good stability with respect to different choices of the basis set. In addition, the MT charge can be easily calculated even at post-Hartree-Fock levels of theory. With the MT charge, it is shown that for a planar water dimer, the charge transfer from the proton acceptor to the proton donor is about -0.052 e. While both planar hydrated cations and anions show signs of charge transfer, anions show a much more significant charge transfer to the hydration water than the corresponding cations. It might be important to explicitly model the ion charge transfer to water in a force field at least for the anions.
进行了密立根油滴实验的原子版本的计算。结果表明,对于平面分子,密立根实验的原子版本可用于定义不受电荷流动贡献影响的原子部分电荷。我们将这个电荷称为密立根-汤姆逊(MT)电荷。由于 MT 电荷与均匀电场下的原子力成正比,因此它是最相关的力场发展电荷。MT 电荷对于不同基组的选择具有很好的稳定性。此外,即使在哈特利-福克理论之后的水平上,也可以很容易地计算 MT 电荷。使用 MT 电荷,我们表明对于平面水二聚体,质子受体到质子供体的电荷转移约为-0.052e。虽然平面水合阳离子和阴离子都显示出电荷转移的迹象,但阴离子向水合水的电荷转移比相应的阳离子明显得多。在力场中至少对阴离子显式地对离子电荷转移到水进行建模可能很重要。