Visinoni R, Giorgianni S, Baldacci A, Ghersetti S
Dipartimento di Chimica Fisica, Università di Venezia, Venezia, I-30123, Italy
J Mol Spectrosc. 1998 Aug;190(2):248-61. doi: 10.1006/jmsp.1998.7598.
The two mid-infrared bands of the CF2&dbond;CHF molecule, nu5 centered at 1172.673 cm-1 and nu6 + nu9 at 1155.105 cm-1, were measured on a tunable diode laser spectrometer with a resolution near the Doppler limit. These vibrations of A' species give rise to a/b hybrid bands, even though our analysis has pointed out that the intensity of the a-type component is predominant. Most of the J and K structure has been resolved in different subbranches, and the rovibrational analysis led to the assignment of about 1400 (J </= 60, Ka </= 22, Kc </= 60) and 90 (J </= 56, Ka </= 5, Kc </= 56) lines of the nu5 and nu6 + nu9 bands, respectively. Using Watson's A-reduction Hamiltonian in the Ir representation, a set of accurate spectroscopic constants for the upper states has been derived from transitions free of major resonance effects. The rotational structure of the nu5 vibration also exhibits effects of Coriolis perturbation by a state identified as nu7 + nu11. Parameters for the perturber were determined from the interaction effects near the observed crossings, using a dyad model including first-order b-Coriolis interaction. Copyright 1998 Academic Press.
在一台分辨率接近多普勒极限的可调谐二极管激光光谱仪上,测量了CF2═CHF分子的两个中红外波段,中心位于1172.673 cm-1的ν5波段和1155.105 cm-1的ν6 + ν9波段。这些A' 类振动产生了a/b混合带,尽管我们的分析指出a型成分的强度占主导。大部分J和K结构已在不同子分支中得到分辨,转动振动分析分别确定了ν5波段和约1400条(J ≤ 60,Ka ≤ 22,Kc ≤ 60)以及ν6 + ν9波段的约90条(J ≤ 56,Ka ≤ 5,Kc ≤ 56)谱线。利用Ir表示中的沃森A约化哈密顿量,从无主要共振效应的跃迁中导出了一组上能级的精确光谱常数。ν5振动的转动结构还表现出被确定为ν7 + ν11的一个态的科里奥利微扰效应。利用包含一阶b - 科里奥利相互作用的并矢模型,根据观测交叉点附近的相互作用效应确定了微扰体的参数。版权所有1998年学术出版社。