VCI Calculations Based on Canonical and Localized Normal Coordinates for Non-Abelian Molecules: Accurate Assignment...

Vibrational configuration interaction calculations (VCI) have been performed to study the impact of the nature of the underlying coordinate systems, i.e., canonical vs localized normal coordinates, on accurate vibrational structure calculations for non-Abelian molecules. Once the correlation space is represented by real-valued primitive Hartree products, the assignment of vibrational states beyond the fundamentals is usually a tedious task and is further complicated by the use of non-symmetry-adapted coordinates. Our recently presented approach based on sparse grid integration of overlap integrals of the VCI wave function with the corresponding harmonic oscillator wave function has been used to determine and assign all fundamentals and vibrational overtones of allene and its deuterated isotopologue. Excellent agreement with available experimental results is observed in all cases.