Photodissociation of triplet and singlet states of the CCO radical

The tripler and singlet states of the ketenylidene (CCO) radical are investigated using fast radical beam photofragment translational spectroscopy, in which CCO is generated by laser photodetachment of CCO- and subsequently photodissociated, and anion photoelectron spectroscopy. In the photodissociation experiment, two bands in which the upper state of CCO predissociates are studied, Photodissociation from excitation of the (A) over tilde (II)-I-3-(X) over tilde(3) Sigma(-) band in CCO is observed from 16 666-23 529 cm(-1); resonances are observed and assigned to excited vibrational levels involving all three vibrational modes. We also report the first observation of the (c) over tilde(1)II-(a) over tilde(1) Delta band in CCO. Here, the (a) over tilde Delta state of CCO is generated by laser photodetachment at higher photon energy than was used to generate the (X) over tilde(3) Sigma state, The (c) over tilde(1)II state is approximately located by photoelectron spectroscopy of CCO-, and the photodissociation experiment shows that the origin of the (c) over tilde(1)II-(a) over tilde(1) Delta band occurs around 17 170 cm(-1). Kinetic-energy release spectra from both bands yield accurate values for the C-CO bond dissociation energy and heat of formation of CCO: D-0(C-CO)=2.24+/-0.02 eV (51.7+/-0.5 kcal/mol) and Delta H-f,298(0)(CCO)=4.04+/-0.02 eV (91.1 +/-0.5 kcal/mol). Although the translational-energy distributions resulting from excitation to the (A) over tilde(3)II and (c) over tilde(1)II states are clearly nonstatistical, consideration of the potential-energy surfaces indicates that dissociation from both states occurs via radiationless transitions to the (X) over tilde(3) Sigma(-) state. (C) 1998 American Institute of Physics.