AN APPROACH TO UNDERSTANDING BOND-LENGTH BOND-ANGLE RELATIONSHIP

被引:18
作者
SHIRLEY, WA
HOFFMANN, R
MASTRYUKOV, VS
机构
[1] CORNELL UNIV, CTR MAT SCI, ITHACA, NY 14853 USA
[2] CORNELL UNIV, CTR THEORY, COMPUTAT SCI & ENGN GRP, ITHACA, NY 14853 USA
[3] UNIV TEXAS, DEPT CHEM & BIOCHEM, AUSTIN, TX 78712 USA
[4] MOSCOW MV LOMONOSOV STATE UNIV, DEPT CHEM, ELECTRON DIFFRACT LAB, MOSCOW 119899, RUSSIA
关键词
D O I
10.1021/j100012a024
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
In many studies the relationship between a bond's length and the angle formed with an adjacent bond has been shown to be inverse; larger bond angles result in shorter bond lengths. Mastryukov and co-workers, however, have found some bonds that lengthen at extreme angles. In this work, the bond length/bond angle relationship was reexamined to gain understanding of the normal behavior and this occasional turnover in behavior at large angles. The correlation between bond lengths and adjacent bond angles in CX(4), CXH(3), and CHX(3) (X = H, Cl, F) has been studied by extended Huckel and air initio Hartree-Fock/STO-3G techniques. In these molecules, the angle between three of the bonds and the fourth unique bond was varied, thus retaining C-3v symmetry. We examined the overlap populations between each of the atoms and the central carbon as a function of angle. In the case of the ab initio calculations, we also allowed all bond lengths to relax. We present arguments to explain the normal and direct behavior on the basis of overlap populations, Walsh diagrams, ab initio Optimized bond lengths, and consideration of the nonbonded, X ... X, interactions. We are able to explain the anomalous behavior at large angles in two ways: (a) from a decomposition of the molecular orbitals and the delicate balance of s and p character in them and (b) from the adjustments the electronic structure makes to the uncomfortably short X ... X contacts.
引用
收藏
页码:4025 / 4033
页数:9
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