Literature DB >> 28009861

Structures of protonated hydrogen sulfide clusters, H+(H2S)n, highlighting the nature of sulfur-centered intermolecular interactions.

Dandan Wang1, Asuka Fujii1.   

Abstract

Unique intermolecular structures of protonated hydrogen sulfide clusters, H+(H2S)n, are revealed by infrared spectroscopy and ab initio calculations. The identified intermolecular structures are significantly different from those of the corresponding protonated water clusters, H+(H2O)n, in spite of the common hydrogen bond coordination ability between hydrogen sulfide and water. Protonated hydrogen sulfide clusters have the Eigen type ion core, H3S+, in the size range of n = 3-9. After the first hydrogen bonded shell formation is completed at n = 4, further solvation prefers a new shell bound by the charge-dipole interaction rather than the second hydrogen bonded shell. Thus, closely solvated structures, in which 7 molecules, at maximum, directly interact with the Eigen type ion core, are formed. The beginning of the second hydrogen bonded shell is found at n = 9. Competition among intermolecular interactions in H+(H2S)n is discussed.

Entities:  

Year:  2017        PMID: 28009861     DOI: 10.1039/c6cp07342e

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  2 in total

1.  Spectroscopic observation of two-center three-electron bonded (hemi-bonded) structures of (H2S) n+ clusters in the gas phase.

Authors:  Dandan Wang; Asuka Fujii
Journal:  Chem Sci       Date:  2017-01-11       Impact factor: 9.825

2.  The S∴π hemibond and its competition with the S∴S hemibond in the simplest model system: infrared spectroscopy of the [benzene-(H2S) n ]+ (n = 1-4) radical cation clusters.

Authors:  Dandan Wang; Keigo Hattori; Asuka Fujii
Journal:  Chem Sci       Date:  2019-06-19       Impact factor: 9.825

  2 in total

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