A quantum state-resolved insertion reaction: O(1D) + H2(j = 0) → OH(2II, v, N) + H(2S)

X. Liu, J. J. Lin, S. Harich, G. C. Schatz, X. Yang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

116 Scopus citations

Abstract

The O(1D) + H2 → OH + H reaction, which proceeds mainly as an insertion reaction at a collisional energy of 1.3 kilocalories per mole, has been investigated with the high-resolution H atom Rydberg 'tagging' time-of-flight technique and the quasiclassical trajectory (QCT) method, Quantum state-resolved differential cross sections were measured for this prototype reaction. Different rotationally-vibrationally excited OH products have markedly different angular distributions, whereas the total reaction products are roughly forward and backward symmetric. Theoretical results obtained from QCT calculations indicate that this reaction is dominated by the insertion mechanism, with a small contribution from the collinear abstraction mechanism through quantum tunneling.

Original languageEnglish (US)
Pages (from-to)1536-1538
Number of pages3
JournalScience
Volume289
Issue number5484
DOIs
StatePublished - Sep 1 2000

ASJC Scopus subject areas

  • General

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