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碲化氢3ν2、ν1 + ν2和ν2 + ν3谱带的高分辨率研究。

High Resolution Study of the 3nu2, nu1 + nu2, and nu2 + nu3 Bands of H2Te.

作者信息

Flaud J, Arcas P, Burger H, Polanz O

机构信息

CNRS, Universite Pierre et Marie Curie, 4, Place Jussieu, Paris Cedex 05, 75252, France

出版信息

J Mol Spectrosc. 1997 Apr;182(2):315-32. doi: 10.1006/jmsp.1996.7204.

Abstract

High-resolution Fourier transform spectra of a natural sample of hydrogen telluride and of monoisotopic H2130Te have been recorded in the 3.2-4-0 μm spectral region where the 3nu2, nu1 + nu2, and nu2 + nu3 bands of this molecule absorb. The (030) rotational levels were least-squares fitted using a Watson-type Hamiltonian whereas it proved necessary to consider the strong Coriolis interaction coupling the (110) and the (011) rotational levels. In this way all the experimental levels were calculated to within their experimental uncertainty and precise sets of vibrational energies and rotational and coupling constants were obtained for the (030), (110), and (011) vibrational states of H2130Te, H2128Te, H2126Te, H2125Te, H2124Te, H2123Te, and H2122Te. The band centers for the most abundant isotopic species, namely H2130Te, are:nuo(3nu2) = 2565.4428, nuo(nu1 + nu2) = 2911.4098, nuo(nu2 + nu3) = 2915.9599 cm-1 Copyright 1997Academic Press

摘要

碲化氢天然样品以及单同位素H₂¹³⁰Te的高分辨率傅里叶变换光谱已在3.2 - 4.0μm光谱区域记录,该分子的3ν₂、ν₁ + ν₂和ν₂ + ν₃带在此区域吸收。使用沃森型哈密顿量对(030)转动能级进行最小二乘拟合,而事实证明有必要考虑耦合(110)和(011)转动能级的强科里奥利相互作用。通过这种方式,所有实验能级的计算误差在实验不确定度范围内,并获得了H₂¹³⁰Te、H₂¹²⁸Te、H₂¹²⁶Te、H₂¹²⁵Te、H₂¹²⁴Te、H₂¹²³Te和H₂¹²²Te的(030)、(110)和(011)振动态的精确振动能、转动常数和耦合常数集。最丰富的同位素物种H₂¹³⁰Te的带中心为:ν₀(3ν₂)=2565.4428,ν₀(ν₁ + ν₂)=2911.4098,ν₀(ν₂ + ν₃)=2915.9599 cm⁻¹ 版权所有1997学术出版社

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