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Chaos in the classical mechanics of bound and quasi- bound HX-~4He complexes with X = F, Cl, Br, CN

机译:X = F,Cl,Br,CN的束缚和拟束缚HX-〜4He络合物经典力学中的混沌

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摘要

The classical dynamics of weakly bound floppy van der Waals complexes have been extensively studied in the past except for the weakest of all, i.e., those involving He atoms. These complexes are of considerable current interest in light of recent experimental work focussed on the study of molecules trapped in small droplets of the quantum solvent ~4He. Despite a number of quantum investigations, details on the dynamics of how quantum solvation occurs remain unclear. In this paper, the classical rotational dynamics of a series of van der Waals complexes, HX-~4He with X = F, Cl, Br, CN, are studied. In all cases, the ground state dynamics are found to be almost entirely chaotic, in sharp contrast to other floppy complexes, such as HCl-Ar, for which chaos sets in only at relatively high energies. The consequences of this result for quantum solvation are discussed. We also investigate rotationally excited states with J = 1 which, except for HCN- He, are actually resonances that decay by rotational pre-dissociation.
机译:过去,弱束缚的范德华复合物的经典动力学已得到广泛研究,但最弱的除外,即涉及He原子的那些。鉴于最近的实验工作集中在研究量子溶剂〜4He的小液滴中捕获的分子,这些络合物目前具有相当大的兴趣。尽管进行了大量的量子研究,关于量子溶剂化如何发生的动力学的细节仍不清楚。本文研究了一系列范德华配合物HX-〜4He,其中X = F,Cl,Br,CN的经典旋转动力学。在所有情况下,都发现基态动力学几乎完全是混乱的,这与诸如HCl-Ar之类的其他松散配合物形成鲜明对比,后者仅在相对较高的能量下才会陷入混乱。讨论了该结果对量子溶剂化的影响。我们还研究了J = 1的旋转激发态,除HCN- He外,它实际上是由于旋转预解离而衰减的共振。

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