Your browser doesn't support javascript.
loading
Roaming Dynamics in the Photodissociation of Formic Acid at 230 nm.
Ma, Yujie; Liu, Jiaxing; Li, Fangfang; Wang, Fengyan; Kitsopoulos, Theofanis N.
Affiliation
  • Ma Y; Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Centre of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , P. R. China.
  • Liu J; Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Centre of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , P. R. China.
  • Li F; Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Centre of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , P. R. China.
  • Wang F; Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Centre of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , P. R. China.
  • Kitsopoulos TN; Department of Dynamics at Surfaces, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany; Institute of Electronic Structure and Laser, FORTH, Heraklion, Greece; Department of Chemistry , University of Crete , Heraklion , Greece.
J Phys Chem A ; 123(17): 3672-3677, 2019 May 02.
Article in En | MEDLINE | ID: mdl-30969120
ABSTRACT
Roaming dynamics is observed in the photodissociation of formic acid (HCOOH) at 230 nm by using the slice imaging method. In combination with rotational state selective (2 + 1) resonance-enhanced multiphoton ionization of the CO fragments, the speed distributions of the CO fragments exhibit a low recoil velocity at low rotational levels of J = 9 and 20, while the velocity distributions of CO at high rotational levels of J = 30 and 48 show a relatively large recoil velocity. The experimental results indicate that the roaming of OH radical should be related with the formation of CO + H2O channel at the present photolysis energy. Unlike the roaming pathways occurring in H2CO that can be described by loose flat potential, our CO speed distribution analysis suggests the presence of a "tight" flat potential in the roaming dynamics of HCOOH molecules.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem A Journal subject: QUIMICA Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem A Journal subject: QUIMICA Year: 2019 Type: Article