Coordination chemistry of (c-C5H5)Fe+ in the gas phase at 294 +/- 3 K: reactions with the inorganic ligands H-2, H2O, NH3, CO, N-2, NO, CO2, N2O, andNO2
V. Baranov et Dk. Bohme, Coordination chemistry of (c-C5H5)Fe+ in the gas phase at 294 +/- 3 K: reactions with the inorganic ligands H-2, H2O, NH3, CO, N-2, NO, CO2, N2O, andNO2, INT J MASS, 204(1-3), 2001, pp. 209-221
Experimental results are reported for primary and higher-order gas-phase re
actions of (c-C5H5)Fe+ with H-2, H2O,NH3, CO, N-2, NO, CO2, N2O, and NO2. R
eaction rate coefficients and product distributions were measured with the
selected-ion how tube technique operating at 294 +/- 3 K and a helium buffe
r-gas pressure of 0.35 +/- 0.01 Torr. The measurements provide intrinsic ef
ficiencies for ligation and lead to intrinsic coordination numbers based on
ligation kinetics. The extent of sequential ligation was found to be stron
gly dependent on the nature of the ligand. Single ligation of the (c-C5H5)F
e+ cation was observed with H-2, N-2, N2O, and CO2 whereas multiple ligatio
n was observed with NO, NO2, CO, H2O, and NH3. With NO2 oxygen-atom transfe
r was the dominant reaction channel. Structures have been proposed for the
ligated ions and relative bond energies were investigated using multicollis
ion induced dissociation. (C) 2001 Elsevier Science B.V.