Electronic structure and UV spectrum of hexachloroplatinate dianions in vacuo

We present a joint experimental and theoretical study of the electronic spectrum of hexachloroplatinate dianion. We have measured electronic photodissociation and photodetachment spectra of mass-selected PtCl62− ions in vacuo and compare these with calculated band positions from time-dependent densi...

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Hauptverfasser: Kaufman, Sydney H. (VerfasserIn) , Weber, J. Mathias (VerfasserIn) , Pernpointner, Markus (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 20 November 2013
In: The journal of chemical physics
Year: 2013, Jahrgang: 139, Heft: 19, Pages: 1-10
ISSN:1089-7690
DOI:10.1063/1.4830407
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1063/1.4830407
Verlag, lizenzpflichtig, Volltext: https://aip.scitation.org/doi/10.1063/1.4830407
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Verfasserangaben:Sydney H. Kaufman, Mathias J. Weber, and Markus Pernpointner
Beschreibung
Zusammenfassung:We present a joint experimental and theoretical study of the electronic spectrum of hexachloroplatinate dianion. We have measured electronic photodissociation and photodetachment spectra of mass-selected PtCl62− ions in vacuo and compare these with calculated band positions from time-dependent density functional theory and from relativistic calculations. Excitation of an electronic transition of the dianion leads to resonant enhancement of the photodetachment cross section superimposed on direct detachment. Photoexcitation results in loss of Cl− and Cl0, depending on photon energy. The photofragmentation spectrum for formation of the PtCl4− fragment ion mirrors the UV/vis absorption spectrum of PtCl62− in solution with a small solvatochromic shift.
Beschreibung:Gesehen am 22.04.2021
Beschreibung:Online Resource
ISSN:1089-7690
DOI:10.1063/1.4830407