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Photoelectron spectroscopy of hexachloroplatinate-nucleobase complexes: Nucleobase excited state decay observed via delayed electron emission.

Authors :
Sen, Ananya
Matthews, Edward M.
Gao-Lei Hou
Xue-Bin Wang
Dessent, Caroline E. H.
Source :
Journal of Chemical Physics; 2015, Vol. 143 Issue 18, p1-8, 8p, 1 Diagram, 4 Charts, 4 Graphs
Publication Year :
2015

Abstract

We report low-temperature photoelectron spectra of isolated gas-phase complexes of the hexachloroplatinate dianion bound to the nucleobases uracil, thymine, cytosine, and adenine. The spectra display well-resolved, distinct peaks that are consistent with complexes where the hexachloroplatinate dianion is largely intact. Adiabatic electron detachment energies for the hexachloroplatinate-nucleobase complexes are measured as 2.26-2.36 eV. The magnitudes of the repulsive Coulomb barriers (RCBs) of the complexes are all ∼1.7 eV, values that are lower than the RCB of the uncomplexed PtCl<subscript>6</subscript><superscript>2-</superscript> dianion as a result of charge solvation by the nucleobases. In addition to the resolved spectral features, broad featureless bands indicative of delayed electron detachment are observed in the 193 nm photoelectron spectra of the four clusters. The 266 nm spectra of the PtCl<subscript>6</subscript><superscript>2-</superscript>·thymine and PtCl<subscript>6</subscript><superscript>2-</superscript>·adenine complexes also display very prominent delayed electron emission bands. These results mirror recent results on the related Pt(CN)<subscript>4</subscript><superscript>2-</superscript>·nucleobase complexes [A. Sen et al., J. Phys. Chem. B 119, 11626 (2015)]. The observation of delayed electron emission bands in the PtCl<subscript>6</subscript><superscript>2-</superscript>·nucleobase spectra obtained in this work, as for the previously studied Pt(CN)<subscript>4</subscript><superscript>2-</superscript>·nucleobase complexes, is attributed to one-photon excitation of nucleobase-centred excited states that can effectively couple to the electron detachment continuum, producing strong electron detachment. Moreover, the selective, strong excitation of the delayed emission bands in the 266 nm spectra is linked to fundamental differences in the individual nucleobase photophysics at this excitation energy. This strongly supports our previous suggestion that the dianion within these clusters can be viewed as a "dynamic tag" which has the propensity to emit electrons when the attached nucleobase decays over a time scale long enough to allow autodetachment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219606
Volume :
143
Issue :
18
Database :
Complementary Index
Journal :
Journal of Chemical Physics
Publication Type :
Academic Journal
Accession number :
111019282
Full Text :
https://doi.org/10.1063/1.4935171