TY - JOUR

T1 - Weakly bound molecular dimers

T2 - Intramolecular vibrational fundamentals, overtones, and tunneling splittings from full-dimensional quantum calculations using compact contracted bases of intramolecular and low-energy rigid-monomer intermolecular eigenstates

AU - Felker, Peter M.

AU - Bačić, Zlatko

N1 - Funding Information:
Z.B. is grateful to the National Science Foundation for its partial support of this research through Grant No. CHE-1566085. P.F. is grateful to Professor Daniel Neuhauser for the generous sharing of his computer resources.
Publisher Copyright:
© 2019 Author(s).

PY - 2019/7/14

Y1 - 2019/7/14

N2 - We present a method for the efficient calculation of intramolecular vibrational frequencies, and their tunneling splittings, in weakly bound molecular dimers, together with the intermolecular vibrational states within each intramolecular vibrational manifold. The approach involves the partitioning of the dimer's vibrational Hamiltonian into two reduced-dimension Hamiltonians, a rigid-monomer one for the intermolecular vibrations and the other for all intramolecular vibrational degrees of freedom, and a remainder. The eigenstates of the two reduced-dimension Hamiltonians are used to build up a product contracted basis for the diagonalization of the full vibrational Hamiltonian. The key idea is that because of weak coupling between inter- and intra-molecular vibrational modes, the full-dimensional eigenstates in the low-energy portions of the manifolds associated with the intramolecular vibrational excitations can be computed accurately in a compact basis that includes a relatively small number of rigid-monomer intermolecular eigenstates, spanning a range of energies much below those of the intramolecular vibrational states of interest. In the application to the six-dimensional (6D) problem of (HF)2, we show that this approach produces results in excellent agreement with those in the literature, with a fraction of the basis states required by other methods. In fact, accurate energies of the intramolecular vibrational fundamentals and overtones are obtained using 6D bases that include 4D rigid-monomer intermolecular vibrational eigenstates extending to only 500-1000 cm-1, far below the HF-stretch fundamental of about 4000 cm-1. The method thus holds particular promise with respect to calculations on complexes with greater numbers of vibrational degrees of freedom.

AB - We present a method for the efficient calculation of intramolecular vibrational frequencies, and their tunneling splittings, in weakly bound molecular dimers, together with the intermolecular vibrational states within each intramolecular vibrational manifold. The approach involves the partitioning of the dimer's vibrational Hamiltonian into two reduced-dimension Hamiltonians, a rigid-monomer one for the intermolecular vibrations and the other for all intramolecular vibrational degrees of freedom, and a remainder. The eigenstates of the two reduced-dimension Hamiltonians are used to build up a product contracted basis for the diagonalization of the full vibrational Hamiltonian. The key idea is that because of weak coupling between inter- and intra-molecular vibrational modes, the full-dimensional eigenstates in the low-energy portions of the manifolds associated with the intramolecular vibrational excitations can be computed accurately in a compact basis that includes a relatively small number of rigid-monomer intermolecular eigenstates, spanning a range of energies much below those of the intramolecular vibrational states of interest. In the application to the six-dimensional (6D) problem of (HF)2, we show that this approach produces results in excellent agreement with those in the literature, with a fraction of the basis states required by other methods. In fact, accurate energies of the intramolecular vibrational fundamentals and overtones are obtained using 6D bases that include 4D rigid-monomer intermolecular vibrational eigenstates extending to only 500-1000 cm-1, far below the HF-stretch fundamental of about 4000 cm-1. The method thus holds particular promise with respect to calculations on complexes with greater numbers of vibrational degrees of freedom.

UR - http://www.scopus.com/inward/record.url?scp=85068773185&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85068773185&partnerID=8YFLogxK

U2 - 10.1063/1.5111131

DO - 10.1063/1.5111131

M3 - Article

C2 - 31301718

AN - SCOPUS:85068773185

SN - 0021-9606

VL - 151

JO - Journal of Chemical Physics

JF - Journal of Chemical Physics

IS - 2

M1 - 024305

ER -