PHOTODISSOCIATION SPECTROSCOPY AND PHOTOFRAGMENT IMAGING OF THE Fe⁺(acetylene) AND Fe⁺(benzene)₁,₂ COMPLEXES TO PROBE DISSOCIATION ENERGIES
Blais, John R. C.
Loading…
Permalink
https://hdl.handle.net/2142/122686
Description
Title
PHOTODISSOCIATION SPECTROSCOPY AND PHOTOFRAGMENT IMAGING OF THE Fe⁺(acetylene) AND Fe⁺(benzene)₁,₂ COMPLEXES TO PROBE DISSOCIATION ENERGIES
Author(s)
Blais, John R. C.
Contributor(s)
Duncan, Michael A
Dynak, Nathan John
Colley, Jason E.
Issue Date
2023-06-23
Keyword(s)
Photodissociation and photochemistry
Abstract
Tunable laser photodissociation spectroscopy and photofragment imaging experiments are employed to investigate the dissociation energies of the Fe⁺(acetylene), Fe⁺(benzene), and Fe⁺(benzene)₂ ion-molecule complexes. In the spectroscopy experiment, continuous dissociation is observed above a certain energy threshold throughout the visible wavelength region for all three complexes. Photofragment imaging of the Fe⁺ photoproduct in the cases of Fe⁺(acetylene) and Fe⁺(benzene), and imaging of the benzene⁺ charge transfer photoproduct of Fe⁺(benzene), provide upper limits on the dissociation energies of these two complexes. The dissociation energies measured from this two-pronged approach agree nicely with values determined previously by collision-induced dissociation. However, these values are inconsistent with those produced from computational chemistry at the DFT level, despite the implementation of functionals recommended for transition metal chemistry.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.