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氦纳米液滴中非交替烃的电子光谱。

Electronic spectroscopy of nonalternant hydrocarbons inside helium nanodroplets.

作者信息

Birer Ozgür, Moreschini Paolo, Lehmann Kevin K, Scoles Giacinto

机构信息

Chemistry Department, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

J Phys Chem A. 2007 Dec 13;111(49):12200-9. doi: 10.1021/jp071175z. Epub 2007 Sep 20.

Abstract

We have recorded the electronic spectra of three polycyclic aromatic hydrocarbons (acenaphtylene, fluoranthene, and benzo(k)fluoranthene) containing a five-member ring and their van der Waals complexes with argon and oxygen with a molecular beam superfluid helium nanodroplet spectrometer. Although the molecules, which differ by addition of one or two fused benzene rings to acenaphtylene, have the same point group symmetry, the spectral lineshapes show distinct differences in the number of zero phonon lines and shapes of the phonon wings. Whereas the smallest molecule (acenaphtylene) has the most complicated line shape, the largest molecule (benzo(k)fluoranthene) shows different lineshapes for different vibronic transitions. The van der Waals complexes of fluoranthene exhibit more peaks than the theoretically allowed number of isomeric complexes with argon/oxygen. The current models of molecular solvation in liquid helium do not adequately explain these discrepancies.

摘要

我们使用分子束超流氦纳米液滴光谱仪记录了三种含有五元环的多环芳烃(苊烯、荧蒽和苯并[k]荧蒽)及其与氩气和氧气形成的范德华复合物的电子光谱。尽管这些分子通过在苊烯上添加一个或两个稠合苯环而有所不同,但它们具有相同的点群对称性,光谱线形在零声子线的数量和声子翼的形状上显示出明显差异。最小的分子(苊烯)具有最复杂的线形,而最大的分子(苯并[k]荧蒽)在不同的振转跃迁中显示出不同的线形。荧蒽的范德华复合物展现出的峰数比理论上允许的与氩气/氧气形成的异构体复合物的数量更多。目前关于液氦中分子溶剂化的模型无法充分解释这些差异。

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