Photodissociation spectroscopy of Mg+-H2O and Mg+-D2O

• Published in: The Journal of chemical physics 1992-12, Vol.97 (12), p.8886-8895
• Main Authors: WILLEY, K. F, YEH, C. S, ROBBINS, D. L, PILGRIM, J. S, DUNCAN, M. A
• Format: Article
• Language: English
• Subjects: Atomic and molecular physics; Exact sciences and technology; Molecular properties and interactions with photons; Photon interactions with molecules; Physics
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.463363

Mg+–H2O ion–molecule complexes are produced in a pulsed supersonic nozzle cluster source. These complexes are mass selected and studied with laser photodissociation spectroscopy in a reflectron time-of-flight mass spectrometer system. An electronic transition assigned as 2B2←X 2A1 is observed with an origin at 28 396 cm−1. The spectrum has a prominent progression in the metal-H2O stretching mode with a frequency (ω′e) of 518.0 cm−1. An extrapolation of this progression fixes the excited state dissociation energy (D′0) at 15 787 cm−1. The corresponding ground state value (D″0) is 8514 cm−1 (24.3 kcal/mol). The solvated bending mode, and symmetric and asymmetric stretching modes of water are also active in the complex, as are the magnesium bending modes. A second electronic transition assigned as 2B1←X 2A1 is observed with an origin at 30 267 cm−1 and a metal stretch frequency for Mg+–H2O of 488.5 cm−1 (ΔG1/2). Spectra of both excited states are also observed for Mg+–D2O. Partially resolved rotational structure is analyzed for both isotopes, leading to the conclusion that the complex has a structure with C2v symmetry. This study was guided by ab initio calculations by Bauschlicher and co-workers, which provide accurate predictions of the electronic transition energies, vibrational constants, and dissociation energies.