| Autor: |
Miller, Thomas M., Viggiano, A. A., Miller, Amy E. Stevens, Morris, Robert A., Henchman, Michael, Paulson, John F., Van Doren, Jane M. |
| Předmět: |
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| Zdroj: |
Journal of Chemical Physics; 4/15/1994, Vol. 100 Issue 8, p5706, 9p |
| Abstrakt: |
We report the first measurements of rate constants for formation and reaction of the hydrated-hydride ion H3O-. We studied the Kleingeld–Nibbering reaction [Int. J. Mass Spectrom. Ion Phys. 49, 311 (1983)], namely, dehydrogenation of formaldehyde by hydroxide to form hydrated-hydride ion and carbon monoxide. The OD-+H2CO reaction is about 35% efficient at 298 K, with OD-/OH- exchange occurring in about half the reactions. H3O- was observed to undergo thermal dissociation in a helium carrier gas at room temperature with a rate constant of 1.6×10-12 cm3 s-1. We also studied a new reaction in which H3O- is formed: The association of OH- with H2 in a He carrier gas at low temperatures. The rate coefficient for this ternary reaction is 1×10-30 cm6 s-1 at 88 K. Rate coefficients and product branching fractions were determined for H3O- reactions with 19 neutral species at low temperatures (88–194 K) in an H2 carrier. The results of ion-beam studies, negative-ion photoelectron spectroscopy, and ion-molecule reaction data allow us to specify the hydride–water bond energy D0298(H--H2O)=14.4±1.0 kcal mol-1 (0.62±0.04 eV). The heat of formation of H3O-, -37.5±1.0 kcal mol-1, and the proton affinity of H3O-, 386.0±1.0 kcal mol-1, are derived from these results. Dissociation of H3O- into OH- and H2 requires 4.5±1.0 kcal mol-1 energy. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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