De. Clemmer et al., STATE-SPECIFIC REACTIONS OF FE-2((A(6)D,A(4)F) WITH D2O AND REACTIONSOF FEO+ WITH D), Journal of physical chemistry, 98(26), 1994, pp. 6522-6529
Reactions of Fe+ with D2O and FeO+ with D-2 are studied as a function
of translational energy in a guided-ion beam tandem mass spectrometer.
In the former system, the only products observed from single-collisio
n events are FeD+ and FeOD+. These products are formed in endothermic
reactions. At low energies, the FeOD2+ adduct is also observed, a resu
lt of secondary stabilizing collisions with D2O. Results for Fe+ produ
ced in two different sources are analyzed to yield state-specific cros
s sections for reaction of the a(6)D ground and a(4)F first excited st
ates of Fe+. In the reaction of FeO+ with D-2, three ionic products (F
e+, FeD+ and FeOD+) are observed. An inefficient exothermic process th
at forms Fe+ + D2O is observed, consistent with known thermochemistry;
however, formation of Fe+ + D2O also occurs via another more efficien
t pathway that involves a reaction barrier of similar to 0.6 eV. The F
eOD+ channel also proceeds via a pathway involving a reaction barrier
of the same energy. Results for both the Fe+ + D2O and FeO+ + D-2 syst
ems are used to derive potential energy surfaces for these systems.