The static and dynamic electronic (hyper)polarizabilities of the equilibrium conformations of 2,2′-bithiophene (anti-gauche and syn-gauche) were computed in the gas phase. The calculations were carried out using Hartree-Fock (HF), Møller-Plesset second-order perturbation theory (MP2), and density functional theory methods. The properties were evaluated for the second harmonic generation (SHG), and electrooptical Pockels effect (EOPE) nonlinear optical processes at the typical =1064 nm of the Nd:YAG laser. The anti-gauche form characterized by the S-C2-C2′-S dihedral angle of 137° (MP2/6-311G) is the global minimum on the potential energy surface, whereas the syn-gauche rotamer (S-C2-C2′-S = 48°, MP2/6-311G) lies ca. 0.5 kcal/mol above the anti-gauche form. The structural properties of the gauche structures are rather similar to each other. The MP2 electron correlation effects are dramatic for the first-order hyperpolarizabilities of the 2,2′-bithiophenes, decreasing the HF values by ca. a factor of three. When passing from the anti-gauche to the syn-gauche conformer, the static and frequency-dependent first-order hyperpolarizabilities increase by ca. a factor of two. Differently, the electronic polarizabilities and second-order hyperpolarizabilities of these rotamers are rather close to each other. The syn-gauche structure could be discriminated from the anti-gauche one through its much more intense SHG and EOPE signals. © 2013 Andrea Alparone.
CITATION STYLE
Alparone, A. (2013). Second harmonic generation, electrooptical pockels effect, and static first-order hyperpolarizabilities of 2,2′-bithiophene conformers: An HF, MP2, and DFT theoretical investigation. Advances in Physical Chemistry, 2013. https://doi.org/10.1155/2013/394697
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