Abstract
The preparation of methyl iodide (CH(3)I) in selected rovibrational states [nu(7)=1 (C-H stretch); J] by infrared (IR) excitation prior to vacuum ultraviolet (VUV) photoionization has greatly simplified the observed pulsed field ionization-photoelectron (PFI-PE) spectra, allowing the direct determination of the rotational constants B(+)(C(+))=0.254+/-0.003 cm(-1) for CH(3)I(+)(X (2)E(3/2);nu(7) (+)) and the ionization energy (76 896.9+/-0.2 cm(-1)) for CH(3)I(+)(X (2)E(3/2);nu(7) (+)=1,J(+)=3/2)<--CH(3)I(X (1)A(1);nu(7)=1,J=0). The IR-VUV-PFI-PE and IR-VUV-photoion measurements also provide relative state-to-state (nu(7) (+)=1, J(+)<--nu(7)=1, J) cross sections for the photoionization process.
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