Acceleration of correlation-corrected vibrational self-consistent field calculation times for large polyatomic molecules

Acceleration of the correlation-corrected Vibrational self-consistent field (CC-VSCF) method for anharmonic calculations of vibrational states of polyatomic molecules is described. The acceleration assumes pairwise additive interactions between different normal modes, and employs orthogonality of the single-mode vibrational wave functions. This greatly reduces the effort in computing correlation effects between different vibrational modes, which is treated by second order perturbation theory in CC-VSCF. The acceleration can improve the scaling of the overall computational effort from N-6 to N-4, where N is the number of vibrational modes. Sample calculation times, using semiempirical potential surfaces (PM3), ire given for a series of glycine peptides. Large Computational acceleration, and significant reduction of the scaling of the effort with system size, is found and discussed.