| Autor: |
Hsu, Po-Jen, Mizuide, Atsuya, Kuo, Jer-Lai, Fujii, Asuka |
| Zdroj: |
Physical Chemistry Chemical Physics (PCCP); 11/21/2024, Vol. 26 Issue 43, p27751-27762, 12p |
| Abstrakt: |
While preferential hydrogen bond network structures of cold protonated alcohol clusters H+(ROH)n are generally switched from a linear type to a cyclic one at n = 4–5, those of protonated 2,2,2-trifluoroethanol (TFE) clusters maintain linear type structures at least in the size range of n = 3–7. To explore the origin of the strong linear type network preference of H+(TFE)n, infrared spectra of protonated mixed clusters H+(TFE)m(ethanol)n (m + n = 5) were measured. An efficient structure sampling technique using parallelized basin-hopping algorithms and deep-learning neural network potentials is developed to search for essential isomers of the mixed clusters. Vibrational simulations based on the harmonic superposition approximation were compared with the observed spectra to identify the major isomer component at each mixing ratio. It was found that the formation of the cyclic structure occurs only in n ≥ 3 of the mixed clusters, in which the proton solvating sites and the double acceptor site are occupied by ethanol. The crucial role of the stability of the double acceptor site in the cyclic structure formation is discussed. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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