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旋转分辨红外光谱法研究超声速喷射冷却异戊二烯。

Rotationally Resolved Infrared Spectroscopy of Supersonic Jet-Cooled Isoprene.

机构信息

Department of Chemistry, Connecticut College, New London, Connecticut 06320, United States.

出版信息

J Phys Chem A. 2023 Jun 8;127(22):4873-4879. doi: 10.1021/acs.jpca.3c02272. Epub 2023 May 26.

Abstract

The high-resolution infrared spectrum of isoprene has been observed under supersonic jet-cooled conditions in the region of the ν vibrational band near 992 cm. The spectrum was assigned and fit using a standard asymmetric top Hamiltonian, and an acceptable fit was obtained for transitions to excited state energy levels with ≤ 6, with an error in the fit of 0.002 cm. For excited state energy levels with > 6, a perturbation was present that prevented fitting using the standard asymmetric top Hamiltonian. Based on previous anharmonic frequency calculations and observed vibrational bands of isoprene, the perturbation is most likely caused by Coriolis coupling between the ν and ν vibrations or a combination band that lies near the ν band. The excited state rotational constants from the fit show reasonable agreement with previous anharmonic calculations performed at the MP2/cc-pVTZ level of theory. The jet-cooled spectrum is compared with previous high-resolution measurements of this band at room temperature and shows that understanding the perturbation will be necessary to accurately model this vibrational band.

摘要

在接近 992cm 的 ν 振动带的超音速射流冷却条件下,观察到了异戊二烯的高分辨率红外光谱。使用标准的非对称转子哈密顿量对光谱进行了赋值和拟合,对于激发态能级的跃迁,拟合得到了 ≤ 6 的可接受结果,拟合误差为 0.002cm。对于激发态能级 > 6,存在一个微扰,使得无法使用标准的非对称转子哈密顿量进行拟合。基于先前的非谐频率计算和异戊二烯观察到的振动带,微扰很可能是由 ν 和 ν 振动之间的科里奥利耦合或位于 ν 带附近的组合带引起的。拟合得到的激发态转动常数与在 MP2/cc-pVTZ 理论水平上进行的先前非谐计算吻合较好。射流冷却光谱与该带在室温下的先前高分辨率测量结果进行了比较,表明要准确模拟该振动带,理解微扰将是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5878/10258839/3de7f6acd681/jp3c02272_0002.jpg

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