Hydrogen-hydrogen bonding: A stabilizing interaction in strained chelating rings of metal complexes in aqueous phase

被引:54
作者
Cukrowski, Ignacy [1 ]
Matta, Cherif F. [2 ,3 ]
机构
[1] Univ Pretoria, Dept Chem, ZA-0002 Pretoria, South Africa
[2] Mt St Vincent Univ, Dept Chem & Phys, Halifax, NS B3M 2J6, Canada
[3] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4J3, Canada
基金
新加坡国家研究基金会; 加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
THEORETICAL ELECTRON-DENSITY; DIHYDROGEN BOND; MECHANICS; MOLECULES; BIPHENYL;
D O I
10.1016/j.cplett.2010.09.013
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
Two H center dot center dot center dot H close contacts, classically associated with steric hindrance, were found to be H-H closed-shell bonding interactions which stabilize a zinc(II) complex with nitrilotri-3-propanoic acid, [Zn(NTPA)(H2O)(2)](-), by ca. 11 kcal/mol in aqueous phase. The strain energy of three 6-member rings (ca. 40 kcal/mol) is significantly offset by these interactions the presence of which is indicated by the presence of a bond path, an elevated delocalization index, and a lowering of the atomic energy of each hydrogen atom involved in an H center dot center dot center dot H interaction by similar to 4-5 kcal/mol. The difference between relevant bond path angles and geometrical bond angles in the 6-member coordination rings correlates well with strain energy and formation constants. Unexpectedly, the bite angle N-Zn-O is found to be the least strained. (c) 2010 Elsevier B. V. All rights reserved.
引用
收藏
页码:66 / 69
页数:4
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