More items are visible when logged in!

Quantum-chemical calculations

  • Quantum-chemical calculation of spectroscopic parameters

    Speaker: Professor Cristina Puzzarini
    Institute: University of Bologna
    Country: Italy
    Speaker Link:

    Cristina Puzzarini

    Department of Chemistry “Giacomo Ciamician”, University of Bologna

    Video Recording

    Video is available only for registered users.


    Implementation of very accurate ab initio methods on one hand and improvements in computer facilities on the other hand allow the determination of structural, molecular, and spectroscopic properties of small- to medium-size molecules to a very high accuracy. The predictive capabilities have such an accuracy that theoretical calculations can guide, support and even challenge experimental determinations. To perform accurate quantum-chemical calculations of spectroscopic parameters, post-HF methods, such as the coupled cluster ones, should be employed in conjunction with extrapolative and additive techniques in order to account for basis set and wave function truncation errors as well as to include important corrections, such as those related to core correlation and vibrational effects.
    Concerning rotational spectra, the starting point is the computation of an accurate equilibrium geometry for the evaluation of the corresponding rotational constants.  Next, quadratic and cubic force constants allow the determination of vibrational corrections to rotational constants together with the quartic and sextic centrifugal-distortion constants. Finally, accurate dipole moment components and, when needed, quadrupole-coupling constants complete the list of the needed quantities. The most effective strategy relies on coupled-cluster (CC) evaluations (at the CC singles and doubles augmented by a perturbative treatment of triple excitations, CCSD(T)) of equilibrium geometries, properties, and, possibly, quadratic force constants in a normal-mode representation (i.e., harmonic frequencies), also considering extrapolation to the complete basis set (CBS) limit and core− valence correlation (CV) contributions. These results can be complemented by density functional theory (DFT) evaluations of the anharmonic contributions (employing hybrid or double hybrid functionals, like B3LYP and B2PLYP, in conjunction with medium-sized basis sets). For larger molecules, benchmark studies suggest that the computationally expensive (and slowly converging) evaluation of harmonic frequencies at the CCSD(T)/CBS level augmented by CV corrections can be replaced by effective B2PLYP computations without any dramatic reduction of the accuracy for both rotational and vibrational spectroscopy investigations.
    Concerning vibrational spectroscopy, the simulation of fully anharmonic spectra including fundamental, overtones, and combination bands  requires, in addition to the quantities discussed above for the rotational spectra, quartic (at least semi-diagonal) force constants together with second and third derivatives of the electric dipoles (for IR spectra). Once again, hybrid and double hybrid functionals perform very well in the computation of anharmonic contributions, provided that, for the evaluation of the electric dipoles, diff use functions are properly included in the basis set. Subsequently, the vibrational problem can be solved by either variational or perturbative approaches. For semi-rigid molecules, second-order vibrational perturbation theory (VPT2) is particularly effective, provided that nearly resonant contributions are treated by means of a variational approach, thus leading to the so-called generalized VPT2 model (GVPT2).