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统一布朗斯特酸度标度的锚点:质子溶剂化标准吉布斯自由能计算的 rCCC 模型在十一种代表性液体介质中的应用。

Anchor points for the unified Brønsted acidity scale: the rCCC model for the calculation of standard Gibbs energies of proton solvation in eleven representative liquid media.

机构信息

Institute for Inorganic and Analytical Chemistry, Freiburger Materialforschungszentrum FMF, Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104 Freiburg, Germany.

出版信息

Chemistry. 2011 May 16;17(21):5808-26. doi: 10.1002/chem.201003164. Epub 2011 May 3.

Abstract

The COSMO cluster-continuum (CCC) solvation model is introduced for the calculation of standard Gibbs solvation energies of protons. The solvation sphere of the proton is divided into an inner proton-solvent cluster with covalent interactions and an outer solvation sphere that interacts electrostatically with the cluster. Thus, the solvation of the proton is divided into two steps that are calculated separately: 1) The interaction of the proton with one or more solvent molecules is calculated in the gas phase with high-level quantum-chemical methods (modified G3 method). 2) The Gibbs solvation energy of the proton-solvent cluster is calculated by using the conductor-like screening model (COSMO). For every solvent, the solvation of the proton in at least two (and up to 11) proton-solvent clusters was calculated. The resulting Gibbs solvation energies of the proton were weighted by using Boltzmann statistics. The model was evaluated for the calculation of Gibbs solvation energies by using experimental data of water, MeCN, and DMSO as a reference. Allowing structural relaxation of the proton-solvent clusters and the use of structurally relaxed Gibbs solvation energies improved the accordance with experimental data especially for larger clusters. This variation is denoted as the relaxed COSMO cluster-continuum (rCCC) model, for which we estimate a 1σ error bar of 10 kJ mol(-1) . Gibbs solvation energies of protons in the following representative solvents were calculated: Water, acetonitrile, sulfur dioxide, dimethyl sulfoxide, benzene, diethyl ether, methylene chloride, 1,2-dichloroethane, sulfuric acid, fluorosulfonic acid, and hydrogen fluoride. The obtained values are absolute chemical standard potentials of the proton (pH=0 in this solvent). They are used to anchor the individual solvent specific acidity (pH) scales to our recently introduced absolute acidity scale.

摘要

COSMO 连续统-介电模型(CCC)被引入到质子标准吉布斯溶剂化能的计算中。质子的溶剂化球被分为具有共价相互作用的内质子-溶剂簇和与簇静电相互作用的外溶剂化球。因此,质子的溶剂化被分为两个单独计算的步骤:1)用高精度量子化学方法(改进的 G3 方法)在气相中计算质子与一个或多个溶剂分子的相互作用。2)用导体相似屏蔽模型(COSMO)计算质子-溶剂簇的吉布斯溶剂化能。对于每种溶剂,至少计算了两个(最多 11 个)质子-溶剂簇的质子溶剂化。质子的吉布斯溶剂化能通过玻尔兹曼统计进行加权。该模型通过使用水、MeCN 和 DMSO 的实验数据作为参考来评估计算吉布斯溶剂化能的效果。允许质子-溶剂簇的结构弛豫和使用结构弛豫的吉布斯溶剂化能显著提高了与实验数据的一致性,特别是对于较大的簇。这种变化被表示为弛豫的 COSMO 连续统-介电模型(rCCC),我们估计其 1σ误差为 10 kJ mol(-1)。计算了以下代表性溶剂中质子的吉布斯溶剂化能:水、乙腈、二氧化硫、二甲亚砜、苯、二乙醚、二氯甲烷、1,2-二氯乙烷、硫酸、氟磺酸和氢氟酸。得到的值是质子在溶剂中的绝对化学标准电势(在该溶剂中 pH=0)。它们用于将每个溶剂特定的酸度(pH)标度锚定到我们最近引入的绝对酸度标度。

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