The CuTe Molecule: Theoretical investigation of the electronic structure and dipole moments of the ground and lowest excited states with rovibrational calculations

The multireference configuration interaction calculation MRSDCI (with Davidson correction) has been performed to investigate the potential energy curves, the transition electronic energies T e , the spectroscopic constants (R e , ω e and B e ), the transition and permanent dipole moments , and the vibrational levels corresponding to the ground and 18 excited electronic states of the molecule CuTe in the representation 2S+1 Λ (+/-) (neglecting the spin–orbit effects), whereas the PECs and the spectroscopic constants have been calculated for 27 states in the representation Ω (+/-) [including the spin–orbit (SO) effects]. The ground state equilibrium bond length and the vibrational frequency have also been investigated using the density functional theory (DFT), where different density functionals with different basis sets have been tested. This study represents the first theoretical study of the excited states of the CuTe molecule. Comparison of the present results with the available experimental ones shows an overall satisfying agreement.