THE XE-CL2 CONUNDRUM - VANDERWAALS COMPLEX OR LINEAR MOLECULE

被引:20
作者
PROSERPIO, DM
HOFFMANN, R
JANDA, KC
机构
[1] CORNELL UNIV,DEPT CHEM,ITHACA,NY 14853
[2] UNIV PITTSBURGH,DEPT CHEM,PITTSBURGH,PA 15260
[3] CORNELL UNIV,CTR MAT SCI,ITHACA,NY 14853
关键词
D O I
10.1021/ja00019a014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present an approximate molecular orbital analysis of the potential energy surface for XeCl2, supported by qualitative perturbation theoretic analysis of the bonding in these species. Three minima are located on the XeCl2 surface: the observed Xe...Cl2 van der Waals complex, the linear Cl-Xe-Cl molecule, and between them an unexpected strongly bent ClXeCl intermediate. The latter is characterized by a qualitatively different electronic configuration and is likely to have barriers between it and the two other potential minima. Possible experimental methods to observe both the intermediate geometry and the linear molecule are discussed. The reaction pathways for the conversion of the van der Waals isomer of XeCl2 to the more stable linear isomer passes through the newly predicted bent isomer and thus proceeds through two curve-crossing regions. This explains why the van der Waals isomer can be observed in the gas phase.
引用
收藏
页码:7184 / 7189
页数:6
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