Complexation of n SO2 molecules (n = 1, 2, 3) with formaldehyde and thioformaldehyde.

Citation data:

The Journal of chemical physics, ISSN: 1089-7690, Vol: 140, Issue: 3, Page: 034302

Publication Year:
2014
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Repository URL:
https://digitalcommons.usu.edu/chem_facpub/615; https://works.bepress.com/steve_scheiner/319
PMID:
25669374
DOI:
10.1063/1.4861432
Author(s):
Azofra, Luis Miguel; Scheiner, Steve
Publisher(s):
AIP Publishing; Hosted by Utah State University Libraries
Tags:
Physics and Astronomy; Chemistry; Complexation; n SO2; Formaldehyde; Thioformaldehyde
article description
Ab initio and density functional theory calculations are used to examine complexes formed between H2CO and H2CS with 1, 2, and 3 molecules of SO2. The nature of the interactions is probed by a variety of means, including electrostatic potentials, natural bond orbital, atoms in molecules, energy decomposition, and electron density redistribution maps. The dimers are relatively strongly bound, with interaction energies exceeding 5 kcal/mol. The structures are cyclic, containing both a O/S⋯S chalcogen bond and a CH⋯O H-bond. Addition of a second SO2 molecule leads to a variety of heterotrimer structures, most of which resemble the original dimer, where the second SO2 molecule engages in a chalcogen bond with the first SO2, and a C⋯O attraction with the H2CX. Some cooperativity is apparent in the trimers and tetramers, with an attractive three-body interaction energy and shortened intermolecular distances.