Ab initio studies of π-water tetramer complexes

Evolution of optimal structures, binding energies, and vibrational spectra of π-(H2O)n (n=1-4) complexes

Tarakeshwar Pilarisetty, Kwang S. Kim, S. Djafari, K. Buchhold, B. Reimann, H. D. Barth, B. Brutschy

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

The optimal structures, binding energies, and harmonic vibrational frequencies of clusters containing a substituted benzene molecule microsolvated by four water molecules, termed as π-(water tetramer) clusters (π: p-difluorobenzene, fluorobenzene, benzene, toluene) have been evaluated at the second order perturbation level of theory (MP2) using both the 6-31+G* and aug-cc-pVDZ basis sets. In sharp contrast to the complexes of smaller water clusters with these π systems, wherein the water subcluster is most strongly bound to toluene, the water tetramer is most strongly bound to fluorobenzene. This exceptionally high binding energy results from both a π⋯OH H-bond and a competing σ F⋯OH bond between the water tetramer moiety and the aromatic molecule. The magnitudes of the many-body energy terms and their contribution to the binding energies of these π-(water tetramer) systems indicates that the contributions of three- and higher-order terms are much smaller when compared to the neutral water clusters. The two-body terms associated with the π- and σ-type of interaction indicates that in both the fluorobenzene and p-difluorobenzene complexes, the increase in the size of the water cluster enhances the π-H-bonding interaction and weakens the σ F⋯H interaction. This observation is in consonance with the calculated and experimentally observed redshifts of the OH vibrational frequencies. Thus, with an increase in the size of a water cluster bound to the fluorinated π system, there is a lowering of the redshift induced by the σ F⋯H interaction and an increase in the redshift due to the π-H interaction. The calculated redshift of the π H-bonded OH mode is very much dependent on the basis set, with larger basis sets yielding shifts which are in better agreement with the experimentally determined shifts.

Original languageEnglish (US)
Pages (from-to)4016-4024
Number of pages9
JournalJournal of Chemical Physics
Volume114
Issue number9
StatePublished - Mar 1 2001
Externally publishedYes

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Vibrational spectra
Binding energy
vibrational spectra
energy spectra
binding energy
Water
Fluorobenzenes
water
Toluene
Benzene
Molecules
interactions
toluene
benzene
molecules
shift
harmonics
perturbation

ASJC Scopus subject areas

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

Cite this

Ab initio studies of π-water tetramer complexes : Evolution of optimal structures, binding energies, and vibrational spectra of π-(H2O)n (n=1-4) complexes. / Pilarisetty, Tarakeshwar; Kim, Kwang S.; Djafari, S.; Buchhold, K.; Reimann, B.; Barth, H. D.; Brutschy, B.

In: Journal of Chemical Physics, Vol. 114, No. 9, 01.03.2001, p. 4016-4024.

Research output: Contribution to journalArticle

Pilarisetty, Tarakeshwar ; Kim, Kwang S. ; Djafari, S. ; Buchhold, K. ; Reimann, B. ; Barth, H. D. ; Brutschy, B. / Ab initio studies of π-water tetramer complexes : Evolution of optimal structures, binding energies, and vibrational spectra of π-(H2O)n (n=1-4) complexes. In: Journal of Chemical Physics. 2001 ; Vol. 114, No. 9. pp. 4016-4024.
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