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Published on: January 4, 2018
Time-resolved gas-phase kinetic study of the germylene addition reaction, GeH(2) + C(2)D(2)
1Instituto de Quimica-Fisica Rocasolano, C.S.I.C., C/Serrano 119, 28006 Madrid, Spain. r.becerra@iqfr.csic.es
Abstract:
Time-resolved studies of germylene, GeH(2), generated by laser flash photolysis of 3,4-dimethyl-1-germacyclopent-3-ene, have been carried out to obtain rate coefficients for its bimolecular reaction with C(2)D(2). The reaction was studied in the gas phase, mainly at a total pressure of 1.3 kPa (in SF(6) bath gas) at five temperatures in the range 298-558 K. Pressure variation measurements over the range 0.13-13 kPa (SF(6)) at 298, 397 and 558 K revealed a small pressure dependence but only at 558 K. After correction for this, the second-order rate coefficients gave the Arrhenius equation: log(k infinity/cm3 molecule(-1) s(-)1) = (-10.96 +/- 0.05) + (6.16 +/- 0.37 kJ mol-1)/RT ln 10. Comparison with the reaction of GeH(2) + C(2)H(2) (studied earlier) showed a similar behaviour with almost identical rate coefficients. The lack of a significant isotope effect is consistent with a rate-determining addition process and is explained by irreversible decomposition of the reaction intermediate to give Ge((3)P) + C(2)H(4). This result contrasts with that for GeH(2) + C(2)H(4)/C(2)D(4) and those for the analogous silylene reactions. The underlying reasons for this are discussed.
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