Infrared Spectroscopy and Structures of Cobalt Carbonyl Cations, Co(CO)(n)(+) (n=1-9)

Abstract

Cobalt carbonyl cations of the form Co(CO)(n)(+) (n = 1-9) are produced in a molecular beam by laser vaporization in a pulsed nozzle source. These ions, and their corresponding "argon-tagged" analogues, Co(CO)(n)(Ar)(m)(+), are studied with mass-selected infrared photodissociation spectroscopy in the carbonyl stretching region. The number of infrared-active bands, their frequency positions, and their relative intensities provide distinctive patterns allowing determination of the geometries and electronic structures of these complexes. CO(CO)(5)(+) has a completed coordination sphere, consistent with its expected 18-electron stability, and it has the same structure (D-3h trigonal bipyramid) as its neutral isoelectronic analog Fe(CO)(5). The carbonyl stretches in CO(CO)(5)(+) are less red-shifted than those in Fe(CO)(5) because of charge-induced reduction in the pi back-bonding. Co(CO)(1-4)(+) complexes have triplet ground states, but the spin changes to a singlet for the Co(CO)(5)(+) complex