J
Jon R. Schoonover
Researcher at Los Alamos National Laboratory
Publications - 102
Citations - 4050
Jon R. Schoonover is an academic researcher from Los Alamos National Laboratory. The author has contributed to research in topics: Excited state & Infrared spectroscopy. The author has an hindex of 40, co-authored 102 publications receiving 3930 citations. Previous affiliations of Jon R. Schoonover include Eastern New Mexico University & University of Ferrara.
Papers
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Journal ArticleDOI
Molecular-Level Electron Transfer and Excited State Assemblies on Surfaces of Metal Oxides and Glass
Thomas J. Meyer,Gerald J. Meyer,Brian W. Pfennig,Brian W. Pfennig,Jon R. Schoonover,Jon R. Schoonover,Cliff J. Timpson,Cliff J. Timpson,Jennifer F. Wall,Jennifer F. Wall,Claus Kobusch,Claus Kobusch,Xiaohong Chen,Xiaohong Chen,Brian M. Peek,Brian M. Peek,Craig G. Wall,Craig G. Wall,Wei Ou,Wei Ou,Bruce W. Erickson,Bruce W. Erickson,Carlo Alberto Bignozzi,Carlo Alberto Bignozzi +23 more
TL;DR: In this article, a general procedure is described for the attachment to antimony-doped tin dioxide (Sb), tin doped indium oxide (In203:Sn), or glass surfaces of molecules with known electron transfer or excited state properties.
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Influence of electronic delocalization in metal-to-ligand charge transfer excited states
Geoffrey F. Strouse,Jon R. Schoonover,Richard Duesing,Stephen Boyde,Wayne E. Jones,Thomas J. Meyer +5 more
TL;DR: In this paper, it was shown that the excited electron in the Ru complex is localized over the bbpe ligand, and that the extended lifetimes are a delocalization effect caused by decreased bond displacement changes in the excited state.
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Electronic coupling in cyano-bridged ruthenium polypyridine complexes and role of electronic effects on cyanide stretching frequencies
Carlo Alberto Bignozzi,Roberto Argazzi,Jon R. Schoonover,Keith C. Gordon,R. Brian Dyer,Franco Scandola +5 more
TL;DR: In this paper, spectroscopic and electrochemical properties of a series of polynuclear complexes containing cyano-bridged ruthenium polypyridine units are consistent with a valence-localized model.
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Application of time-resolved infrared spectroscopy to electronic structure in metal-to-ligand charge-transfer excited states.
TL;DR: D density functional theory calculations on the ground and excited states of fac-[Re(I)(bpy)(CO)3(4-Etpy)](+) provide assignments for the nu(CO) modes in the MLCT excited state and support the importance of pi(4,4'-X2bpy*-)-pi( CO) mixing.
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Time-Resolved Vibrational Spectroscopy of Electronically Excited Inorganic Complexes in Solution.
TL;DR: Time-resolved vibrational spectroscopic studies of electronic excited states in solution were reviewed by Morris and Woodruff in 1987 and with the advances made recently in TRIR spectroscopy, infrared spectra can now be measured on the time scales previously obtained only by the transient Raman method.