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    Characterization of Large-Amplitude Motions and Hydrogen Bonding Interactions in the Thiophene–Water Complex by Rotational Spectroscopy

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    Date
    2021-04-21
    Author
    Silva, Weslley G. D. P.
    van Wijngaarden, Jennifer
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    Abstract
    The rotational fingerprint of the thiophene–water complex was investigated for the first time using Fourier transform microwave spectroscopy (7–20 GHz) aided by quantum mechanical calculations. Transitions for a single species were observed and the rotational constants for the parent and 18O isotopomers are consistent with a geometry that is highly averaged over a barrierless large amplitude motion of water that interconverts two equivalent forms corresponding to the global minimum (B2PLYP-D3(BJ)/def2-TZVP). In this effective geometry, the water lies above the thiophene ring close to its σv plane of symmetry. The observed transitions are split by a second water-centered tunneling motion that exchanges its two protons by internal rotation about its C2 axis with a calculated barrier of ~2.7 kJ mol-1 (B2PLYP-D3(BJ)/def2-TZVP). Based on quantum theory of atoms in molecules, non covalent interaction and symmetry-adapted perturbation theory analyses, the observed geometry enables two intermolecular interactions (O–H…π and O–H…S) whose electrostatic and dispersive contributions favour formation of the thiophene-water complex.
    URI
    http://hdl.handle.net/1993/36042
    DOI
    10.1021/acs.jpca.1c02086
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    • Faculty of Science Scholarly Works [209]
    • University of Manitoba Scholarship [1981]

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