The binding energies of one and two water molecules to the first transition-row metal positive ions. II
- 1 February 1990
- journal article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 92 (3) , 1876-1878
- https://doi.org/10.1063/1.458068
Abstract
The binding energy of H2O to transition-metal ions is determined not only by the electrostatic interaction, but by 4s4p and 3d4s hybridization and by 4s to 3d promotion on the metal. All of the M(H2O)+2 systems are linear except for Mn(H2O)+2 and Zn(H2O)+2, which we show to be bent with 7A1 and 2A1 ground states, respectively. The O–Mn–O bond angle is 94° and the O–Zn–O bond angle is 99°. These systems bend to allow 4s4p hybridization, which reduces the repulsion. For Mn+, the 3dn4s1–3dn+1 separation is too large to allow 3d4s hybridization or 4s to 3d promotion. For Zn+ the ground-state 3d104s1 occupation precludes 4s to 3d promotion or 3d4s hybridization.Keywords
This publication has 7 references indexed in Scilit:
- Production of hydrated metal ions by fast ion or atom beam sputtering. Collision-induced dissociation and successive hydration energies of gaseous copper+ with 1-4 water moleculesJournal of the American Chemical Society, 1989
- The binding energies of one and two water molecules to the first transition-row metal positive ionsThe Journal of Chemical Physics, 1989
- Gas-phase water and hydroxyl binding energies for monopositive first-row transition metal ionsJournal of the American Chemical Society, 1989
- Sequential solvation of atomic transition-metal ions. The second solvent molecule can bind more strongly than the firstJournal of the American Chemical Society, 1989
- A modified coupled pair functional approachThe Journal of Chemical Physics, 1986
- The coupled pair functional (CPF). A size consistent modification of the CI(SD) based on an energy functionalThe Journal of Chemical Physics, 1985
- Gaussian Basis Set for Molecular Wavefunctions Containing Third-Row AtomsThe Journal of Chemical Physics, 1970