화학공학소재연구정보센터
Journal of the American Chemical Society, Vol.124, No.46, 13896-13902, 2002
Evidence for orbital-specific electron transfer to oriented haloform molecules
Beams of hyperthermal K atoms cross beams of the oriented haloforms CF3H, CCl3H, and CBr3H, and transfer of an electron mainly produces K+ and the X- halide ion which are detected in coincidence. As expected, the steric asymmetry of CCl3H and CBr3H is very small and the halogen end is more reactive. However, even though there are three potentially reactive centers on each molecule, the F- ion yield in CF3H is strongly dependent on orientation. At energies close to the threshold for ion-pair formation (similar to5.5 eV), H-end attack is more reactive to form F-. As the energy is increased, the more productive end switches, and F-end attack dominates the reactivity. In CF3H near threshold the electron is apparently transferred to the sigma*(CH) antibonding orbital, and small signals are observed from electrons and CF3- ions, indicating "activation" of this orbital. In CCl3H and CBr3H the steric asymmetry is very small, and signals from free electrons and CX3- ions are barely detectable, indicating that the sigma*(CH) antibonding orbital is not activated. The electron is apparently transferred to the sigma(CX)* orbital which is believed to be the LUMO. At very low energies the proximity of the incipient ions probably determines whether salt molecules or ions are formed.