Vibrational mode selectivity in hyperfine interactions:: Polarization quantum beat spectroscopy of HCF((A)over-tilde1A")

被引:17
作者
Ionescu, I
Fan, HY
Annesley, C
Xin, J
Reid, SA
机构
[1] Marquette Univ, Dept Chem, Milwaukee, WI 53201 USA
[2] Bloomsburg Univ Penn, Dept Phys & Engn Technol, Bloomsburg, PA 17815 USA
关键词
D O I
10.1063/1.1640994
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
We report on the vibrational mode dependence of the F-19 and H-1 hyperfine interaction constants in the A(1)A(') state of HCF, determined using polarization quantum beat spectroscopy. The nuclear spin/overall rotation coupling constants display a pronounced energy dependence and mode selectivity which can be traced to variations in both the A rotational constant and nuclear spin/electron orbital coupling constant a. In particular, modes containing C-F stretching excitation display significantly larger F-19 spin-rotation constants, which is explained in terms of a decrease in back donation of electron density into the C 2p(pi) orbitals. (C) 2004 American Institute of Physics.
引用
收藏
页码:1164 / 1167
页数:4
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