Spectroscopy and reactivity of size-selected Mg+-ammonia clusters

• Published in: The Journal of chemical physics Vol. 121; no. 17; pp. 8375 - 8384
• Main Authors: Lee, James I., Sperry, David C., Farrar, James M.
• Format: Journal Article
• Language: English
• Published: United States 01.11.2004
• Subjects: AMMONIUM COMPOUNDS; ATOMIC CLUSTERS; BRANCHING RATIO; CHEMICAL BONDS; DISSOCIATION; GROUND STATES; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; INTERNAL CONVERSION; MAGNESIUM COMPOUNDS; MAGNESIUM IONS; PHOTON-MOLECULE COLLISIONS; PHOTONS; REACTIVITY; SOLVATION; SOLVENTS; SPECTRA; SPECTRAL SHIFT; SPECTROSCOPY; VIBRATIONAL STATES
• ISSN: 0021-9606; 1089-7690
• DOI: 10.1063/1.1802498

Photodissociation spectra for mass-selected Mg+(NH3)n clusters for n=1 to 7 are reported over the photon energy range from 7000 to 38 500 cm−1. The singly solvated cluster, which dissociates primarily via a N–H bond cleavage, exhibits a resolved vibrational structure corresponding to two progressions in the intracluster Mg+–NH3 modes. The addition of the second, third, and fourth solvent molecules results in monotonic redshifts that appear to halt near 8500 cm−1, where a sharp feature in the electronic spectrum is correlated with the formation of a Mg+(NH3)4 complex with Td symmetry and the closing of the first solvation shell. The spectra for the clusters with 5 to 7 solvent molecules strongly resemble that for the tetramer, suggesting that these solvent molecules occupy a second solvation shell. The wavelength-dependent branching-ratio measurements show that increasing the photon energies generally result in the loss of additional solvent molecules but that enhancements for a specific solvent number loss may reveal special stability for the resultant fragments. The majority of the experimental evidence suggests that the decay of these clusters occurs via the internal conversion of the initially excited electronic states to the ground state, followed by dissociation. In the case of the monomer, the selective cleavage of a N–H bond in the solvent suggests that this internal-conversion process may populate regions of the ground-state surface in the vicinity of an insertion complex H–Mg+–NH2, whose existence is predicted by ab initio calculations.