Intramolecular symmetry-adapted perturbation theory with a single-determinant wavefunction

We introduce an intramolecular energy decomposition scheme for analyzing non-covalent interactions within molecules in the spirit of symmetry-adapted perturbation theory (SAPT). The proposed intra-SAPT approach is based upon the Chemical Hamiltonian of Mayer [Int. J. Quantum Chem. 23(2), 341-363 (1983)] and the recently introduced zeroth-order wavefunction [ J. F. Gonthier and C. Corminboeuf, J. Chem. Phys. 140(15), 154107 (2014)]. The scheme decomposes the interaction energy between weakly bound fragments located within the same molecule into physically meaningful components, i.e., electrostatic-exchange, induction, and dispersion. Here, we discuss the key steps of the approach and demonstrate that a single-determinant wavefunction can already deliver a detailed and insightful description of a wide range of intramolecular non-covalent phenomena such as hydrogen bonds, dihydrogen contacts, and pi - pi stacking interactions. Intra-SAPT is also used to shed the light on competing intra-and intermolecular interactions.


Published in:
Journal of Chemical Physics, 143, 22, 224107
Year:
2015
Publisher:
American Institute of Physics
ISSN:
0021-9606
Laboratories:




 Record created 2015-11-18, last modified 2018-12-03


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