论文标题

在AR存在下,二氧化碳弯曲模式的对称破坏模式

Symmetry breaking of the bending mode of CO2 in the presence of Ar

论文作者

Gartner, T. A., Barclay, A. J., McKellar, A. R. W., Moazzen-Ahmadi, N.

论文摘要

在二氧化碳NU3基本振动区域(〜2340 cm-1)的区域中检测到与(0111)< - (0110)二氧化碳相对应的弱红外光谱(0110),使用可调的Opo laser激光源来探测脉冲的Supersonic Supersonic SliT SLIT SLIT SLIT SLIT SLIT SLIT SLIT SLIT SLIT SLIT EXPATION。 While this method was previously thought to cool clusters to the lowest rotational states of the ground vibrational state, here we show that under suitable jet expansion conditions, sufficient population remains in the first excited bending mode of CO2 (1-2%) to enable observation of vibrationally hot CO2-Ar, and thus to investigate the symmetry breaking of the intramolecular bending mode of CO2 in the presence of Ar.二氧化碳单体的弯曲模式将其分裂为平面和平面模式,并通过科里奥利相互作用牢固地连接。频谱的分析可直接测量平面 /平面外分裂为0.8770 cm-1。进行计算以确定我们结果的关键特征,即两种分子内弯曲模式的能量变化的符号和幅度与量子化学势能表面一致。分子内相互作用的这一方面几乎没有得到以前的实验和理论考虑。因此,我们提供了一种额外的途径,可以通过该途径研究弯曲模式中这种最简单二聚体的分子内动力学。对于其他弱结合的复合物,应该可能会出现类似的结果。

The weak infrared spectrum of CO2-Ar corresponding to the (0111) <-- (0110) hot band of CO2 is detected in the region of the carbon dioxide nu3 fundamental vibration (~2340 cm-1), using a tunable OPO laser source to probe a pulsed supersonic slit jet expansion. While this method was previously thought to cool clusters to the lowest rotational states of the ground vibrational state, here we show that under suitable jet expansion conditions, sufficient population remains in the first excited bending mode of CO2 (1-2%) to enable observation of vibrationally hot CO2-Ar, and thus to investigate the symmetry breaking of the intramolecular bending mode of CO2 in the presence of Ar. The bending mode of CO2 monomer splits into an in-plane and an out-of-plane mode, strongly linked by a Coriolis interaction. Analysis of the spectrum yields a direct measurement of the in-plane / out-of-plane splitting measured to be 0.8770 cm-1. Calculations were carried to determine if key features of our results, i.e., the sign and magnitude of the shift in the energy for the two intramolecular bending modes, are consistent with a quantum chemical potential energy surface. This aspect of intramolecular interactions has received little previous experimental and theoretical consideration. Therefore, we provide an additional avenue by which to study the intramolecular dynamics of this simplest dimer in its bending modes. Similar results should be possible for other weakly-bound complexes.

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