Experiments in
Bradforth lab
utilize ultrafast laser techniques to investigate the coupling between the
solvent and solute in ICN photodissociation.
The interpretation of the data
heavily depends on the spectral assignment of transient species present of
the solution. Of special interest is the CN radical, for which conflicting
spectral assignments appeared in literature.
Electronic structure of open-shell species in water is a theoretically
difficult problem due to (i) large size of the system, (ii) high level of
theory required for their proper description. The avenue to progress lead
via a combination of classical molecular dynamics and electrostatic
treatment of water. The study revealed an expected blue shift of the
B2Σ+←X2Σ+
transition.
Electronic specrum of the
A2Π←X2Σ+
transition of the CN radical in water
Maximum at 1.44 eV.
The interaction with solvent results in the blue-shifted and widened
absorption lineshape (by 0.12 and 0.19 eV, respectively).
Related Publications
44. P. A. Pieniazek, S. E. Bradforth, and A. I. Krylov
Spectroscopy of the cyano radical in an aqueous environment
J. Phys. Chem. A 110, 4854 – 4865
(2006)
Abstract
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