Getting down to the Fundamentals of Hydrogen Bonding: Anharmonic Vibrational Frequencies of (HF)2 and (H2O)2 from Ab Initio Electronic Structure Computations

J Coleman Howard; Jessica L Gray; Amanda J Hardwick; Linh T Nguyen; Gregory S Tschumper

doi:10.1021/ct500860v

Getting down to the Fundamentals of Hydrogen Bonding: Anharmonic Vibrational Frequencies of (HF)2 and (H2O)2 from Ab Initio Electronic Structure Computations

J Chem Theory Comput. 2014 Dec 9;10(12):5426-35. doi: 10.1021/ct500860v.

Authors

J Coleman Howard¹, Jessica L Gray¹, Amanda J Hardwick¹, Linh T Nguyen¹, Gregory S Tschumper¹

Affiliation

¹ Department of Chemistry and Biochemistry, University of Mississippi , University, Mississippi 38677-1848 United States.

PMID: 26583226
DOI: 10.1021/ct500860v

Abstract

This work presents a systematic investigation into the basis set convergence of harmonic vibrational frequencies of (H2O)2 and (HF)2 computed with second-order Møller-Plesset perturbation theory (MP2) and the coupled-cluster singles and doubles method with perturbative connected triples, CCSD(T), while employing correlation-consistent basis sets as large as aug-cc-pV6Z. The harmonic vibrational frequencies presented here are expected to lie within a few cm(-1) of the complete basis set (CBS) limit. For these important hydrogen-bonding prototype systems, a basis set of at least quadruple-ζ quality augmented with diffuse functions is required to obtain harmonic vibrational frequencies within 10 cm(-1) of the CBS limit. In addition, second-order vibrational perturbation theory (VPT2) anharmonic corrections yield CCSD(T) vibrational frequencies in excellent agreement with experimental spectra, differing by no more than a few cm(-1) for the intramonomer fundamental vibrations. D0 values predicted by CCSD(T) VPT2 computations with a quadruple-ζ basis set reproduce the experimental values of (HF)2 and (H2O)2 to within 2 and 21 cm(-1), respectively.