Photoelectron Spectroscopy of Nickel, Palladium, and Platinum Oxide Anions

The 364-nm negative ion photoelectron spectra of XO and OXO molecules (X=Ni, Pd, and Pt) are reported. The spectra yield the electron affinities (EAs): EA(NiO)=1.455±0.005 eV; EA(PdO)=1.672±0.005 eV; EA(PtO)=2.172±0.005 eV; EA(ONiO)=3.043±0.005 eV; EA(OPdO)=3.086±0.005 eV; EA(OPtO)=2.677±0.005 eV. I...

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Veröffentlicht in:Journal of molecular spectroscopy 2002-11, Vol.216 (1), p.1-14
Hauptverfasser: Ramond, Tanya M, Davico, Gustavo E, Hellberg, Fredrik, Svedberg, Fredrik, Salén, Peter, Söderqvist, Patrick, Lineberger, W.Carl
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Sprache:eng
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Zusammenfassung:The 364-nm negative ion photoelectron spectra of XO and OXO molecules (X=Ni, Pd, and Pt) are reported. The spectra yield the electron affinities (EAs): EA(NiO)=1.455±0.005 eV; EA(PdO)=1.672±0.005 eV; EA(PtO)=2.172±0.005 eV; EA(ONiO)=3.043±0.005 eV; EA(OPdO)=3.086±0.005 eV; EA(OPtO)=2.677±0.005 eV. In addition, for the diatomics, transitions from the anion X̃ 2Π 3/2 and X̃′ 2Π 1/2 states into neutral X̃ 3Σ −, 3Π, and for NiO and PdO, 1Π, are assigned. Several states have been reassigned from those in the existing literature. Anion 2Π 3/2– 2Π 1/2 spin–orbit splittings are measured, as are neutral 3Π 2– 3Π 1 spin–orbit splittings: the XO 3Π 2– 3Π 1 splittings increase from 405±30 cm −1 (NiO) to 805±30 cm −1 (PdO) to 3580±40 cm −1 (PtO). A bond length shortening of 0.03±0.01 Å is measured upon electron detachment from NiO −, resulting in an anion bond length of 1.66±0.01 Å. The bond length does not change upon electron detachment from PdO − using 3.4-eV photons. The Pt–O bond length decreases by 0.035±0.010 Å in the 3Π 1← 2Π 3/2 transition. The spectrum of OPtO displays a significantly more extended vibrational progression than those of ONiO or OPdO, and the O–Pt bond length is found to decrease by 0.07±0.01 Å upon electron detachment. The spectra support the view that the Ni–O bond is largely ionic, the Pd–O bond is somewhat less so, and the Pt–O bond displays a substantial covalent character.
ISSN:0022-2852
1096-083X
DOI:10.1006/jmsp.2002.8669