Journal of Physical Chemistry A, Vol.113, No.49, 13742-13751, 2009
Experimental and Theoretical Investigation of the Charge-Separation Energies of Hydrated Zinc(II): Redefinition of the Critical Size
In the preceding article, the hydration energies of Zn2+(H2O)(n) Complexes, where n = 6-10, were measured using threshold collision-induced dissociation (CID) in a guided ion beam tandem mass spectrometer (GIBMS) coupled with an electrospray ionization (ESI) source. The present investigation explores the charge-separation processes observed, Zn2+(H2O)(n) -> ZnOH+(H2O)(m) + H+(H2O)(n-m-1), and the competition between this process and the loss of water. Our results demonstrate that charge-separation processes Occur at variable complex sizes of it = 6, 7, and 8, prompting a redefinition of the critical size for charge separation. Experimental kinetic energy-dependent cross sections are analyzed to yield 0 K threshold energies for the charge-separation products and the effects of competition with this channel oil the energies for losing one and two water ligands after accounting for multiple collisions, kinetic shifts, and energy distributions. A complete reaction coordinate is calculated for the it = 7 complex dissociating into ZnOH+(H2O)(3) + H+(H2O)(3). Calculated rate-limiting transition states for n = 6-8 are also compared to experimental threshold measurements for the charge-separation processes.