Correlation between Bond-Length Change and Vibrational Frequency Shift in Hydrogen-Bonded Complexes Revisited

被引:9
|
作者
Zhang Yu [1 ]
Ma Ning [1 ]
Wang Wei-Zhou [1 ]
机构
[1] Luoyang Normal Univ, Coll Chem & Chem Engn, Luoyang 471022, Henan Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen-bonded complex; Correlation; Bond-length change; Vibrational frequency shift; Density functional theory; HYBRID DENSITY FUNCTIONALS; NONCOVALENT INTERACTIONS; LARGE MOLECULES; LONG-RANGE; ACCURACY; THERMODYNAMICS; APPLICABILITY; ENERGIES; COST;
D O I
10.3866/PKU.WHXB201112303
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 correlation between the X - H bond-length change and the corresponding X - H stretching frequency shift upon X - H center dot center dot center dot Y (Y is an electron donor) hydrogen bond formation is the basis for the spectroscopic detection and investigation of the hydrogen bond. However, this view has been questioned in a recent report, suggesting that the widely accepted correlation between the bond-length change and the frequency shift in hydrogen-bonded complexes is unreliable (McDowell, S. A. C.; Buckingham, A. D. J. Am. Chem. Soc. 2005, 127, 15515.). In this work, several robust computational methods have been used to investigate this issue. The results clearly show that a computational artifact leads to the conclusion incorrectly reported by McDowell and Buckingham and that the correlation between the X - H bond-length change and the corresponding X - H stretching frequency shift is still very good in the hydrogen-bonded complexes studied.
引用
收藏
页码:499 / 503
页数:5
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