These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Photodissociation of S2 (X3Σg-, a1Δg, and b1Σg+) in the 320-205 nm Region.
    Author: Sun ZF, Farooq Z, Parker DH, Martin PJJ, Western CM.
    Journal: J Phys Chem A; 2019 Aug 15; 123(32):6886-6896. PubMed ID: 31322887.
    Abstract:
    Photodissociation of vibrationally and electronically excited sulfur dimer molecules (S2) has been studied in a combined experimental and computational quantum chemistry study in order to characterize bound-continuum transitions. Ab initio quantum chemistry calculations are carried out to predict the potential energy curves, spin-orbit coupling, transition moments, and bound-continuum spectra of S2 for comparison with the experimental data. The experiment uses velocity map imaging to measure S-atom production following S2 photoexcitation in the ultraviolet region (320-205 nm). A pulsed electric discharge in H2S produces ground-state S2 X3Σg-(v = 0-15) as well as electronically excited singlet sulfur and b1Σg+(v = 0, 1), and evidence is presented for the production and photodissociation of S2 a1Δg. In a previous paper, we reported threshold photodissociation of S2X3Σg-(v = 0) in the 282-266 nm region. In the present study, S(3PJ) fine structure branching and angular distributions for photodissociation of S2 (X3Σg-(v = 0), a1Δg and b1Σg+) via the B″3Πu, B3Σu- and 11Πu excited states are reported. In addition, photodissociation of the X3Σg-(v = 0) state of S2 to the second dissociation limit producing S(3P2) + S(1D) is characterized. The present results on S2 photodynamics are compared to those of the well-studied electronically isovalent O2 molecule.
    [Abstract] [Full Text] [Related] [New Search]