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Observation and interpretation of a time-delayed mechanism in the hydrogen exchange reaction

Althorpe, S.C.; Fernandez-Alonso, F.; Bean, B.D.; Ayers, J.D.; Pomerantz, A.E.; Zare, R.N.; Wrede, E.

Authors

S.C. Althorpe

F. Fernandez-Alonso

B.D. Bean

J.D. Ayers

A.E. Pomerantz

R.N. Zare



Abstract

Extensive theoretical(1-13) and experimental(2,13-22) studies have shown the hydrogen exchange reaction H + H-2 --> H-2 + H to occur predominantly through a 'direct recoil' mechanism: the H-H bonds break and form concertedly while the system passes straight over a collinear transition state, with recoil from the collision causing the H-2 product molecules to scatter backward. Theoretical predictions agree well with experimental observations of this scattering process(15-20,22). Indirect exchange mechanisms involving H-3 intermediates have been suggested to occur as well(8-13), but these are difficult to test because bimolecular reactions cannot be studied by the femtosecond spectroscopies(23) used to monitor unimolecular reactions. Moreover, full quantum simulations of the time evolution of bimolecular reactions have not been performed. For the isotopic variant of the hydrogen exchange reaction, H + D-2 --> HD + D, forward scattering features(21) observed in the product angular distribution have been attributed(21,12) to possible scattering resonances associated with a quasibound collision complex. Here we extend these measurements to a wide range of collision energies and interpret the results using a full time-dependent quantum simulation of the reaction, thus showing that two different reaction mechanisms modulate the measured product angular distribution features. One of the mechanisms is direct and leads to backward scattering, the other is indirect and leads to forward scattering after a delay of about 25 femtoseconds.

Citation

Althorpe, S., Fernandez-Alonso, F., Bean, B., Ayers, J., Pomerantz, A., Zare, R., & Wrede, E. (2002). Observation and interpretation of a time-delayed mechanism in the hydrogen exchange reaction. Nature, 416(6876), 67-70. https://doi.org/10.1038/416067a

Journal Article Type Article
Publication Date 2002-03
Deposit Date Apr 12, 2007
Journal Nature
Print ISSN 0028-0836
Electronic ISSN 1476-4687
Publisher Nature Research
Peer Reviewed Peer Reviewed
Volume 416
Issue 6876
Pages 67-70
DOI https://doi.org/10.1038/416067a
Public URL https://durham-repository.worktribe.com/output/1572114