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• W2440314827 abstract "Raman vibrational shifts of small parahydrogen (pH2), orthodeuterium (oD2), and paratritium (pT2) clusters with respect to the free molecules are calculated by combining a first order perturbation theory approach with Langevin equation Path Integral Ground State (LePIGS) simulations [J. Phys. Chem. A 2013, 117, 7461]. Our theoretical predictions are compared to existing cryogenic free jet expansion results for pure (pH2)N clusters [Phys. Rev. Lett. 2004, 92, 223401] and to new measurements for (oD2)N clusters reported here. This method has been successfully used before to predict the Raman vibrational shifts of (pH2)N clusters [J. Chem. Phys. 2014, 141, 014310]. The 6-D interaction potential of Hinde [J. Chem. Phys. 2008, 128, 154308] is reduced to 1-D using the Adiabatic Hindered Rotor approximation to yield effective pair potentials for both molecules being in the ground vibrational state, and for one of them carrying one quantum of vibrational excitation. These reduced 1-D potentials are fitted to a Morse Long Range analytic form for later convenience. Good agreement between experiment and theory is found for the smaller clusters, but significant deviations remain for the larger ones." @default.
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• W2440314827 date "2015-11-12" @default.
• W2440314827 modified "2023-10-14" @default.
• W2440314827 title "Raman Vibrational Shifts of Small Clusters of Hydrogen Isotopologues" @default.
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• W2440314827 doi "https://doi.org/10.1021/acs.jpca.5b08852" @default.
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