Near ultraviolet photodissociation spectroscopy of Mn(+)(H2O) and Mn(+)(D2O).

The electronic spectra of Mn(+)(H2O) and Mn(+)(D2O) have been measured from 30,000 to 35,000 cm(-1) using photodissociation spectroscopy. Transitions are observed from the (7)A1 ground state in which the Mn(+) is in a 3d(5)4s(1) electronic configuration, to the (7)B2 (3d(5)4py) and (7)B1 (3d(5)4px) excited states with T0 = 30,210 and 32,274 cm(-1), respectively. Each electronic transition has partially resolved rotational and extensive vibrational structure with an extended progression in the metal-ligand stretch at a frequency of ∼450 cm(-1).

Vibrational spectroscopy of Co⁺(CH₄)n and Ni⁺(CH₄)n (n = 1-4).

Vibrational spectra of M(+)(CH4)m(Ar)(3-m) and M(+)(CH4)n (M = Co, Ni; m = 1, 2; n = 3, 4) in the C-H stretching region (2500-3100 cm(-1)) are measured using photofragment spectroscopy, monitoring the loss of argon or methane. Interaction with the metal leads to large red shifts in the C-H stretches for proximate hydrogens. The extent of this shift is sensitive to the coordination (η(2) vs η(3)) and to the metal-methane distance.