Multiphoton ionization and photoelectron spectroscopy of formaldehyde via its 3p Rydberg states

The resonance-enhanced multiphoton ionization (REMPI) spectrum of formaldeh yde, two photon resonant in the region of the (1)A(2)(3p(x)), (1)A(1)(3p(y) ), and B-1(2)(3p(z)) states, is reported. The (1)A(2)(3p(x)) state spectrum is dominated by the nu (')(3) (CH2 scissors), nu (4)' (CH2 out-of-plane be nding), nu (')(5) (CH2 asymmetric stretching), and nu (')(6) (CH2 rock) mod es, with weaker bands observed for excitation of the nu (2)' (CO stretching ) mode. Vibrational analysis of the spectrum provides many new frequencies for the (1)A(2)(3p(x)) state, not resolved or accessible in single photon s pectroscopic measurements. Photoelectron spectroscopy is used to probe the nature of the vibronic levels associated with the (1)A(2)(3p(x)) intermedia te state, to measure vibrational frequencies of the resulting cations, and to identify useful routes for preparing vibrational state-selected H2CO+. I t is found that H2CO[(1)A(2)(3p(x))] is a well-behaved Rydberg state, gener ating cations in the same vibrational level that was populated in the inter mediate. Cations with mode-selective excitation of up to 0.62 eV can be pro duced. Ab initio calculations are used to help assign the cation vibrations . In contrast to the well-behaved (1)A(2)(3p(x)) state, the (1)A(1)(3p(y)) and B-1(2)(3p(z)) states are strongly mixed with each other and with valenc e states. (C) 2001 American Institute of Physics.