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High resolution spectroscopic studies of sulfur-32 trioxide (O-16) and sulfur-34 trioxide (O-16).

机译:高分辨光谱学研究三氧化硫32(O-16)和三氧化硫34(O-16)。

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摘要

The two sulfur isotopomers of sulfur trioxide, 32S 16O3 and 34S16O3, have been studied via high resolution infrared and Coherent anti-Stokes Raman (CARS) spectroscopy. The ν1 symmetric SO stretching Q-branches observed by the latter are quite different, being especially complex for 32S16O3. Understanding this band structure required analysis of infrared-active hot bands originating from the ν2 and ν4 bending mode levels to the states 2ν2 (l = 0), ν2 + ν 4 (l= ±1), and 2ν4 (l = 0, ±2). These upper states are strongly coupled to the ν 1 symmetric stretching mode levels via Fermi resonance and indirect Coriolis interactions, causing the CARS spectra of these two molecules to be highly perturbed and quite different in appearance.; From the analysis of 11000 32S16O 3 and 7000 34S16O3 infrared transitions, accurate rovibrational constants have been determined for these mixed states, leading to respective values for ν1, aB1 , and aC1 of 1064.924(11), 0.000 840 93(64), and 0.000 418 19(58) cm −1 for 32S16O3 and 1064.920(84), 0.000 834 5(54), and 0.000 410(11) cm−1 for 34S16O3. These parameters reproduce the respective CARS spectra very well and permit determination of accurate rotational constants for the equilibrium structure of SO3. The results are Be values of 0.349 763 96(64) and 0.349 760 61(334) cm−1 and re values of 141.734 027(130) and 141.734 704(677) pm for 32S 16O3 and 34S16O3 respectively, values that agree within the uncertainties of the measurements. The structure of SO3 is thus one of the best determined configurations of any nonlinear polyatomic molecules.; As part of the analysis, the infrared-active ν2 and ν 4 bending modes were found to be strongly coupled via Coriolis and l-resonance interactions. These interactions cause noticeable wavenumber and intensity perturbations in the ν2, ν4 spectra. Although the emphasis of this work was to fit the transitions, an accompanying analysis of the intensities yielded an average value of ±0.62(8) for the dipole derivative ratio (∂μx/∂Q 4x)/(∂μz/∂Q2) and a positive sign for the product of this ratio with the ζy 24 Coriolis constant, for which experiment gives ±0.5940(15). The sign of individual terms are not determinable from experiment but ab initio calculations were done which indicate that the signs of ∂μ x/∂Q4x and ∂μz/∂ Q2 are both positive and hence ζy 24 is also positive.
机译:三氧化硫的两个硫同位素异构体, 32 S 16 O 3 34 S 16 O 3 。后者观察到的ν 1 对称SO拉伸 Q 分支有很大不同,对于 32 S 16 特别复杂。 super> O 3 。要了解这种能带结构,就需要分析从ν 2 和ν 4 弯曲模式能级到状态2ν 2 的红外活动热带( l = 0),ν 2 4 l =±1)和2ν 4 l = 0,±2)。这些较高的状态通过费米共振和间接科里奥利相互作用强烈地耦合到ν 1 对称拉伸模态水平,从而使这两个分子的CARS光谱受到高度干扰,并且在外观上存在很大差异。通过分析11000 32 S 16 O 3 和7000 34 S 16 O 3 红外跃迁,已经为这些混合态确定了精确的振动常数,从而得出ν 1 a B 1 a C 1 分别为1064.924(11),0.000 840 93(64)和0.000 418 19(58)cm -1 32 S 16 O 3 和1064.920(84),0.000 834 5(54)和0.000 410(11)cm −1 表示 34 S 16 O 3 。这些参数很好地再现了各自的CARS光谱,并可以确定SO 3 平衡结构的精确旋转常数。结果为 B e 值0.349 763 96(64)和0.349 760 61(334)cm -1 r <对于 32 S 16 O 3 的sub> e 值为141.734 027(130)和141.734 704(677)pm sub>和 34 S 16 O 3 ,这些值在测量的不确定性内是一致的。因此,SO 3 的结构是任何非线性多原子分子的最佳确定构型之一。作为分析的一部分,发现红外活动的ν 2 和ν 4 弯曲模式通过科里奥利和 l 共振强烈耦合。互动。这些相互作用在ν 2 ,ν 4 光谱中引起明显的波数和强度扰动。尽管这项工作的重点是适应过渡,但伴随强度的分析得出的偶极导数比(∂μ x /∂ Q的平均值为±0.62(8) 4x )/(∂μ z /∂ Q 2 )和一个正号该比率与ζ y 24 科里奥利常数的乘积,实验得出±0.5940(15)。单个术语的符号不能从实验中确定,而是进行了从头算起计算,这表明∂μ x /∂ Q < sub> 4x 和∂μ z /∂ Q 2 均为正,因此ζ y 24 也是肯定的。

著录项

  • 作者

    Barber, Jeffrey Brian.;

  • 作者单位

    Oregon State University.;

  • 授予单位 Oregon State University.;
  • 学科 Chemistry Physical.; Physics Molecular.; Physics Atmospheric Science.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 p.3293
  • 总页数 124
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
  • 关键词

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