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• W2890919700 endingPage "39" @default.
• W2890919700 startingPage "28" @default.
• W2890919700 abstract "Theoretical studies of the potential energy surfaces (PESs) and bound state calculations were performed for Ar–AgX (X = F, Cl, Br, and I) complexes. A two-dimensional intermolecular PES was constructed at the level of single and double excitation coupled-cluster method with a non-iterative perturbation treatment of triple excitations [CCSD(T)] plus aug-cc-pVQZ basis set supplemented with bond functions for each complex. The global minimum was assigned as the collinear structure of Ar–Ag–X, while the local minimum was assigned as the anti-linear structure of Ar–X–Ag. Both Ar–Ag and Ar–X distances display us an increasing trend from Ar–AgF to Ar–AgI complexes. Based on the bound state results, the intermolecular vibrational modes of collinear and anti-linear isomers were studied in detail via the wavefunction analysis. Due to the very low well depth for the anti-linear structure, an obvious delocalization effect was observed for each complex, except for Ar–AgI. Furthermore, our calculated results suggest that the anti-linear isomer of Ar–AgBr and Ar–AgI could be observed in experiment. The rotational energy levels were also determined based on the ab initio PESs via the bound state calculations. The microwave spectrum for the collinear isomer of each complex was predicted with the maximal percentage error of 1.55% for the complex Ar–AgF. A simple method of coordinate translation was used to re-interpolate the PES for each isotopomer to determine the isotope effects for Ar–AgX complexes and the deduced results are in good agreement with those of experimental observation. The microwave spectrum can be much better reproduced with an equivalent percentage error of 0.07% cm−1 for each isotopomer based on a scaled PES. Finally, we checked the effects of the basis set superposition error (BSSE) correction and core correlation, and found that the BSSE correction has great influence on the intermolecular interactions for the Ar–AgX complexes." @default.
• W2890919700 created "2018-09-27" @default.
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• W2890919700 date "2018-11-01" @default.
• W2890919700 modified "2023-10-02" @default.
• W2890919700 title "Theoretical studies of Ar–AgX (X = F, Cl, Br, I) complexes: Potential energy surfaces, intermolecualr vibrations and microwave spectra" @default.
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• W2890919700 doi "https://doi.org/10.1016/j.jms.2018.09.001" @default.
• W2890919700 hasPublicationYear "2018" @default.
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