Site-dependent photodissociation of vibronically excited CD3 NH2 molecules

Ran Marom, Tal Weiss, Salman Rosenwaks, Ilana Bar

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The mechanism of H and D atom loss, following ultraviolet photolysis of methylamine- d3, CD3 NH2, has been studied via electronic action and Doppler spectroscopies. The N-H bond is preferentially cleaved and the yield of both H and D photofragments increases gradually, but differently, as higher vibrational states on the first excited electronic state, Ã, are accessed, leading to some drop in H/D branching ratios. The average translational energies of the H photofragments are somewhat higher than those of D, implying lower energy content left in the internal degrees of freedom of the CD3 NH than in the CD2 NH2 partner fragment. These results provide evidence for discrimination between the two channels and mechanistic insight into the N-H and C-D bond cleavage.

Original languageEnglish
Article number244310
JournalJournal of Chemical Physics
Volume132
Issue number24
DOIs
StatePublished - 28 Jun 2010

ASJC Scopus subject areas

  • General Physics and Astronomy
  • Physical and Theoretical Chemistry

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