High-resolution infrared spectroscopy of acrolein: The 91, 81, 71, and 61 fundamentals and other vibrational states between 1250 and 1650 cm-1

被引:0
作者
McKellar, A. R. W. [1 ]
Billinghurst, B. E. [2 ]
机构
[1] Natl Res Council Canada, Ottawa, ON K1A 0R6, Canada
[2] Univ Saskatchewan, Canadian Light Source, 44 Innovat Blvd, Saskatoon, SK S7N 0X4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Acrolein; Propenal; Infrared; Synchrotron; Coriolis; Perturbation; MICROWAVE-SPECTRUM; TRANS-ACROLEIN; ABSORPTION SPECTRA; DIPOLE-MOMENT; S-TRANS; CIS; CONSTANTS; CH2CHCHO;
D O I
10.1016/j.jms.2021.111563
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Vibrational states of trans-acrolein (propenal) between 1250 and 1650 cm (-1) are analyzed using high-resolution (asymptotic to 0.001 cm (-1)) infrared absorption spectra. There are four fundamentals in this range, all of which have A ' symmetry: v(9), v(8), v(7), and v(6). Six additional states are directly observed via hot or combination bands: v(10) + v(18), v(9) + v(18), v(8) + v(18), v(7) + v(18), v(16) + v(17), and v(15) + v(17). These ten vibrational states are analyzed in two large multi-state fits, along with 25 additional states which are not directly observed but which affect the observed states by means of many perturbations. The fits involve a total of 239 adjustable variables and account for 6030 (out of 6108) assigned lines with an average error of < 0.0004 cm( -1). But there are about 53 further vibrational states in the region of interest which are not included here. Due to this high density of states, the multi-state fits are incomplete, as well as cumbersome and not unique. Therefore individual fits for each of the four fundamentals are also described, but even with many perturbed transitions omitted they fit much less well.
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页数:7
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