The reaction between silylene and ammonia: Some gas-phase kinetic and quantum chemical studies

Abstract

Time-resolved kinetic studies of the reaction of silylene, SiH2, generated by 193 nm laser flash photolysis of silacyclopent-3-ene, have been carried out in the presence of ammonia, NH3. Second order kinetics were observed. The reaction was studied in the gas phase at 10 Torr total pressure in SF6 bath gas at each of the three temperatures, 299, 340 and 400 K. The second order rate constants (laser pulse energy of 60 mJ +) fitted the Arrhenius equation: $${\rm log}(k/{\rm cm}^3 {\rm molecule}^{-1} {\rm s}^{-1}) = (-10.37 \pm 0.17) + (0.36 \pm 1.12\, {\rm kJ mol}^{-1})/{\rm RT}\,{\rm In}$$ noindent Experiments at other pressures showed that these rate constants were unaffected by pressure in the range 10–100 Torr, but showed small decreases in value at 3 and 1 Torr. There was also a weak intensity dependence, with rate constants decreasing at laser pulse energies of 30 mJ +. Ab initio calculations at the G3 level of theory, show that SiH2+NH3 should form an initial adduct (donor-acceptor complex), but that energy barriers are too great for further reaction of the adduct. This implies that SiH2+NH3 should be a pressure dependent association reaction. The experimental data are inconsistent with this and we conclude that SiH2 decays are better explained by reaction of SiH2 with the amino radical, NH2, formed by photodissociation of NH3 at 193 nm. The mechanism of this previously unstudied reaction is discussed.