Table of Contents
Journal of Quantum Chemistry
Volume 2014, Article ID 860179, 8 pages
http://dx.doi.org/10.1155/2014/860179
Research Article

Anharmonic Spectroscopic Investigation of Tellurophene and Its Perdeuterated Isotopomer: Application of Second-Order Perturbation Theory

Department of Chemistry, University of Catania, Viale A. Doria 6, 95125 Catania, Italy

Received 15 July 2013; Revised 25 September 2013; Accepted 25 September 2013; Published 2 January 2014

Academic Editor: Daniel Glossman-Mitnik

Copyright © 2014 Andrea Alparone. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Vibrational spectra of tellurophene and of its perdeuterated isotopomer were computed using the DFT-B3LYP functional with the LANL2DZ(d,p) basis set. The frequencies of fundamental and overtone transitions were obtained in vacuum under the harmonic approximation and anharmonic second-order perturbation theory (PT2). On the whole the anharmonic corrections reduce the harmonic wavenumber values, in many cases better reproducing the observed fundamental frequencies. The largest anharmonic effects are found for the C–H and C–D stretching vibrations, characterized by relatively high anharmonic coupling constants (up to ca. 120 cm−1). For the C–H/C–D stretches, the harmonic H→D isotopic frequency red-shifts overestimate the observed data by 47–63 cm−1 (5.9–8.1%), whereas the PT2 computations exhibit significantly better performances, predicting the experimental data within 1–19 cm−1 (0.1–2.4%).