A two-step quadrature-based variational calculation of ro-vibrational levels and wavefunctions of CO using a bisector- molecule-fixed frame.

In this paper, we propose a new two-step strategy for computing ro-vibrational energy levels and wavefunctions of a triatomic molecule and apply it to CO. A two-step method [J. Tennyson and B. T. Sutcliffe, , 1986, , 1067] uses a basis whose functions are products of -dependent "vibrational" functions and symmetric top functions. is the quantum number for the molecule-fixed component of the angular momentum. For a linear molecule, a two-step method is efficient because the Hamiltonian used to compute the basis functions includes the largest coupling term. The most important distinguishing feature of the two-step method we propose is that it uses an associated Legendre basis and quadrature rather than a -dependent discrete variable representation. This reduces the cost of the calculation and simplifies the method. We have computed ro-vibrational energy levels with up to 100 for CO, on an accurate available potential energy surface which is known as the AMES-2 PES and present a subset of those levels. We have converged most levels up to 20 000 cm to 0.0001 cm.