Molecular beam measurements of the rotational state distribution of reactively scattered products: RbBr from Rb + HBr

Mosch, J.E.; Safron, S. A.; Toennies, J. P.

doi:10.1016/0009-2614(74)80123-5

Cited by 23 publications

(1 citation statement)

References 13 publications

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“…model parameters describing the dependence of reaction probability on collision energy and approach distance (10); on alignment of state-selected reagent molecules (1 1); variation of the total reaction cross section with collision energy (12) and vibrational (13) or rotational (14) excitation; and analysis of the velocity (IS), rotational energy (16), and spatial orientation of angular momentum (17) of the reactively scattered salt molecules. For several M + H X systems, the electron-jump process has been directly observed, in collisional production of ion-pairs (18) and also in electron spin resonance spectra of a matrix-isolated u * radical corresponding to the HC1-K+ complex (19).…”

Section: Introductionmentioning

confidence: 99%

Molecular beam kinetics: reactions of H and D atoms with alkali halides

Siska¹,

Herschbach²

1994

Can. J. Chem.

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Angular distributions of alkali atoms produced in crossed-beam reactions of H and D atoms (at -2800 K) with KF, CsF, KC1, CsC1, and KBr (at -1100-1200 K) have been measured. For these systems, the reaction exoergicity varies from ADo -17 kcall mol for H + KF to -4 kcaVmol for H + KBr; the thermal distribution of the reactant energy peaks near 12 kcallmol with E -9 kcaYmo1 in relative translation and W -3 kcallmol in vibration and rotation of the alkali halide. Kinematic analysis of the data is canied out by means of a least-squares procedure that includes averaging over the parent beam velocity distributions. The main results are (1) The reaction cross sections Q, vary from -1 to 30 A ' . The magnitude correlates with ADO and with the identity of the halogen for a given alkali, decreasing as F -+ C1+ Br. For a given halogen, Q, is 2-3 times larger for the Cs reaction than for K and about 2 times larger for D than for H. (2) Temperature-dependence measurements for the CsCl case indicate the activation energy (in excess of endoergicity) is near zero. (3) The preferred direction of the reactively scattered alkali atoms with respect to the incident alkali halide varies with the halogen, from mainly forward for the KBr reaction to more sideways for the KF and CsF reactions. (4) The partitioning of energy between product translation E' (M relative to HX) and internal excitation W' (vibration and rotation of HX) can only be roughly estimated; our data are consistent with E' -Wand W' -E + ADo but a definitive analysis will require product velocity distributions or spectra. These results are discussed in terms of a dynamical model akin to Polanyi's DIPR model. This postulates that the motion of H or D is approximately separable from that of the heavier atoms and the preferred reaction geometry corresponds to a triangular H-X-M complex. [Traduit par la rtdaction]

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