Liu Ying, Liu Wenqing, Li Haiyang, Liu Jianguo, Yang Yong
Key Laboratory of Environmental Optical & Technology, Anhui Institute of Optics & Fine Mechanics, Chinese Academy of Sciences, Hefei 230031, P. R. China.
J Phys Chem A. 2006 Oct 19;110(41):11760-4. doi: 10.1021/jp060908x.
The hydrogen bonding interactions of the HNO dimer have been investigated using ab initio molecular orbital and density functional theory (DFT) with the 6-311++G(2d,2p) basis set. The natural bond orbital (NBO) analysis and atom in molecules (AIM) theory were applied to understand the nature of the interactions. The interrelationship between one N-H...O hydrogen bond and the other N-H...O hydrogen bond has been established by performing partial optimizations. The dimer is stabilized by the N-H...O hydrogen bonding interactions, which lead to the contractions of N-H bonds as well as the characteristic blue-shifts of the stretching vibrational frequencies nu(N-H). The NBO analysis shows that both rehybridization and electron density redistribution contribute to the large blue-shifts of the N-H stretching frequencies. A quantitative correlations of the intermolecular distance H...O (r(H...O)) with the parameters: rho at bond critical points (BCPs), s-characters of N atoms in N-H bonds, electron densities in the sigma*(N-H), the blue-shift degrees of nu(N-H) are presented. The relationship between the difference of rho (|Deltarho|) for the one hydrogen bond compared with the other one and the difference of interaction energy (DeltaE) are also illustrated. It indicates that for r(H...O) ranging from 2.05 to 2.3528 A, with increasing r(H...O), there is the descending tendency for one rho(H...O) and the ascending tendency for the other rho(H...O). r(H...O) ranging from 2.3528 to 2.85 A, there are descending tendencies for the two rho(H...O) with increasing r(H...O). On the potential energy surface of the dimer, the smaller the difference between one rho(H...O) and the other rho(H...O) is, the more stable the structure is. As r(H...O) increases, the blue-shift degrees of nu(N-H) decrease. The cooperative descending tendencies in s-characters of two N atoms with increasing r(H...O) contribute to the decreases in blue-shift degrees of nu(N-H). Ranging from 2.05 to 2.55 A, the increase of the electron density in one sigma*(N-H) with elongating r(H...O) weakens the blue-shift degrees of nu(N-H), simultaneously, the decrease of the electron density in the other sigma*(N-H) with elongating r(H...O) strengthens the blue-shift degrees of nu(N-H). Ranging from 2.55 to 2.85 A, the cooperative ascending tendencies of the electron densities in two sigma*(N-H) with increasing r(H...O) contribute to the decreases in blue-shift degrees of nu(N-H).
使用从头算分子轨道和密度泛函理论(DFT)以及6 - 311++G(2d,2p)基组,对HNO二聚体的氢键相互作用进行了研究。应用自然键轨道(NBO)分析和分子中的原子(AIM)理论来理解相互作用的本质。通过进行部分优化,建立了一个N - H...O氢键与另一个N - H...O氢键之间的相互关系。二聚体通过N - H...O氢键相互作用而稳定,这导致N - H键的收缩以及伸缩振动频率ν(N - H)的特征蓝移。NBO分析表明,重新杂化和电子密度重新分布都对N - H伸缩频率的大蓝移有贡献。给出了分子间距离H...O(r(H...O))与键临界点(BCPs)处的ρ、N - H键中N原子的s特征、σ*(N - H)中的电子密度、ν(N - H)的蓝移程度等参数之间的定量相关性。还说明了一个氢键与另一个氢键相比的ρ差值(|Δρ|)与相互作用能差值(ΔE)之间的关系。结果表明,对于r(H...O)在2.05至2.3528 Å范围内,随着r(H...O)增加,一个ρ(H...O)呈下降趋势,另一个ρ(H...O)呈上升趋势。对于r(H...O)在2.3528至2.85 Å范围内,随着r(H...O)增加,两个ρ(H...O)均呈下降趋势。在二聚体的势能面上,一个ρ(H...O)与另一个ρ(H...O)之间的差值越小,结构越稳定。随着r(H...O)增加,ν(N - H)的蓝移程度减小。随着r(H...O)增加,两个N原子的s特征协同下降趋势导致ν(N - H)蓝移程度减小。在2.05至2.55 Å范围内,随着r(H...O)伸长,一个σ*(N - H)中的电子密度增加会削弱ν(N - H)的蓝移程度,同时,随着r(H...O)伸长,另一个σ*(N - H)中的电子密度减小会增强ν(N - H)的蓝移程度。在2.55至2.85 Å范围内,随着r(H...O)增加,两个σ*(N - H)中的电子密度协同上升趋势导致ν(N - H)蓝移程度减小。