15min:

C. LINTON, Centre for Laser Atomic and Molecular Sciences and Physics Department, University of New Brunswick, Fredericton, NB, Canada E3B 5A3; A. G. ADAM, L. E. DOWNIE, A. D. GRANGER, Centre for Laser Atomic and Molecular Sciences and Department of Chemistry, University of New Brunswick, Fredericton, NB, Canada E3B 6E2 ; A. J. ROSS, P. CROZET, Laboratoire de Spectrométrie Ionique et Moléculaire (UMR 5579 CNRS), Bâtiment A. Kastler, Université Lyon I, Domaine Scientifique de la Doua, 69622 Villeurbanne Cedex, France; W. S. HOPKINS, The University Chemical Laboratory, Department of Chemistry, Univeristy of Cambridge, Lensfield Road, Cambridge, UK, CB2 1EW .

High resolution excitation spectra have been obtained of the 0-0 band of the B ~²A₁ X ²A₁ transition of four isotopologues, CaO¹²CH₃, CaO¹³CH₃, CaO¹²CD₃ and CaO¹³CD₃ of calcium monomethoxide. The deuterated species were found to have unexpectedly complicated spectra, and definitive rotational assignments were possible only from investigation by optical optical double resonance (OODR) population depletion spectroscopy. This confirmed the assignment of the CaO¹²CD₃ spectrum, and proved crucial in assigning the K structure and spin components for CaO¹³CD₃. The B ~²A₁ state was found to be well described by the symmetric rotor model with C_3v symmetry for both hydride species but, for the deuterides, the K-structure and spin rotation splittings were irregular, especially for CaO¹³CD₃ where the K = 0 and 1 levels were heavily perturbed. The results of the OODR experiments will be presented, highlighting the assignment, K structure, spin rotation splitting and perturbations in the B ~²A₁ state of the deuterides.