Photoelectron spectroscopy of hexachloroplatinate-nucleobase complexes: Nucleobase excited state decay observed via delayed electron emission
- 1. Department of Chemistry, University of York, Heslington, York YO10 5DD (United Kingdom)
- 2. Physical Sciences Division, Pacific Northwest National Laboratory, MS K8-88, P.O. Box 999, Richland, Washington 99352 (United States)
Description
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 PtCl62− 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 PtCl62− ⋅ thymine and PtCl62− ⋅ adenine complexes also display very prominent delayed electron emission bands. These results mirror recent results on the related Pt(CN)42− ⋅ nucleobase complexes [A. Sen et al., J. Phys. Chem. B 119, 11626 (2015)]. The observation of delayed electron emission bands in the PtCl62− ⋅ nucleobase spectra obtained in this work, as for the previously studied Pt(CN)42− ⋅ 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
Additional details
Identifiers
- DOI
- 10.1063/1.4935171;
Publishing Information
- Journal Title
- Journal of Chemical Physics
- Journal Volume
- 143
- Journal Issue
- 18
- Journal Page Range
- p. 184307-184307.8
- ISSN
- 0021-9606
- CODEN
- JCPSA6
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47063356
- Subject category
- S74: ATOMIC AND MOLECULAR PHYSICS; S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADENINES; CARBON NITRIDES; COMPLEXES; COULOMB FIELD; CYANIDES; CYTOSINE; ELECTRON DETACHMENT; ELECTRON EMISSION; ELECTRONS; EV RANGE; EXCITATION; EXCITED STATES; PHOTOELECTRON SPECTROSCOPY; PHOTONS; PLATINUM CHLORIDES; SOLVATION; THYMINE
- Descriptors DEC
- AMINES; ANTIMETABOLITES; AROMATICS; AZAARENES; AZINES; BOSONS; CARBON COMPOUNDS; CHLORIDES; CHLORINE COMPOUNDS; DRUGS; ELECTRIC FIELDS; ELECTRON SPECTROSCOPY; ELEMENTARY PARTICLES; EMISSION; ENERGY LEVELS; ENERGY RANGE; ENERGY-LEVEL TRANSITIONS; FERMIONS; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC COMPOUNDS; HYDROXY COMPOUNDS; LEPTONS; MASSLESS PARTICLES; NITRIDES; NITROGEN COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; PLATINUM COMPOUNDS; PLATINUM HALIDES; PNICTIDES; PURINES; PYRIMIDINES; SPECTROSCOPY; TRANSITION ELEMENT COMPOUNDS; URACILS
Optional Information
- Notes
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