Guided ion beam mass spectrometry is used to examine the kinetic energ
y dependence of reactions of the second row transition metal cations,
Y+, Zr+, Nb+, and Mo+, with molecular hydrogen and its isotopologues.
By using a meter long flow tube ion source, we are able to create Zr+,
Nb+, and Mof ions that are believed to be in their electronic ground
state terms and primarily in the lowest spin-orbit levels and Y+ mostl
y in its ground state. Corresponding state-specific reaction cross sec
tions are obtained. Analysis of the cross section data yields 0 K bond
dissociation energies of D-0(Y+-H) = 2.65 +/- 0.08 eV, D-0(Zr+-H) = 2
.26 +/- 0.08 eV, D-0(Nb+-H) = 2.28 +/- 0.07 eV, and D-0(Mo+-H) 1.72 +/
- 0.06 eV. This thermochemistry is compared with theoretical calculati
ons and previous experimental measurements. Results for the HD reactio
ns indicate that Y+(D-3) reacts via a statistical mechanism, Zr+(F-4),
Nb+(D-5), and Mo+(S-6) react via largely statistical mechanisms, and
Y+(S-1) shows complex behavior. The reaction mechanisms and reactivity
differences among these ions are explained by using simple molecular
orbital concepts and by referring to potential energy surfaces calcula
ted by Das and Balasubramanian.