Articles you may be interested inExploring the dynamics of reaction N + SiH 4 with crossed molecular-beam experiments and quantum-chemical calculations

We applied the velocity map imaging technique under high-resolution conditions to study ion pair products of the vacuum ultraviolet photodissociation of methyl chloride. We obtained rotationally resolved kinetic energy release spectra that directly provide vibrational frequencies and rotational constants of the fundamental carbocation, CH3+. The technique is analogous to photoelectron spectroscopy, with the chloride anion playing the role of a "heavy electron." The approach shows promise as a general probe of ionic species not amenable to study by traditional methods.

We showcase the use of high-resolution ion imaging with complementary state-resolved and "universal" vacuum ultraviolet probes to address a broad range of fundamental problems in chemical reaction dynamics. Examples from our recent work include applications in state-correlated unimolecular reactions, ion pair dissociation dynamics and spectroscopy, crossed-beam reactive scattering, and atomic angular momentum polarization in photodissociation. These studies are all directed to achieving a detailed understanding of atomic and molecular interactions, with particular emphasis on reaction mechanisms outside the scope of transition state theory; on spectroscopy and dynamics of highly excited, transient species; on nonadiabatic reaction mechanisms; and on chemical dynamics in polyatomic systems.