O
Oanh P. Lam
Researcher at University of Erlangen-Nuremberg
Publications - 23
Citations - 1284
Oanh P. Lam is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: Uranium & Spectral line. The author has an hindex of 19, co-authored 23 publications receiving 1173 citations. Previous affiliations of Oanh P. Lam include University of California, San Diego & Lawrence Berkeley National Laboratory.
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Journal ArticleDOI
Concerted proton-electron transfer in the oxidation of hydrogen-bonded phenols.
Ian J. Rhile,Todd F. Markle,Hirotaka Nagao,Antonio G. DiPasquale,Oanh P. Lam,Mark A. Lockwood,Katrina Rotter,James M. Mayer +7 more
TL;DR: Three phenols with pendant, hydrogen-bonded bases (HOAr-B) have been oxidized in MeCN with various one-electron oxidants, among the first detailed analyses of CPET reactions where the proton and electron move to different sites.
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Insights into the mechanism of carbonate formation through reductive cleavage of carbon dioxide with low-valent uranium centers
TL;DR: Uranium(IV) bridging oxo complexes have been determined to be the intermediate in these transformations.
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Structural and spectroscopic characterization of a charge-separated uranium benzophenone ketyl radical complex.
TL;DR: The reaction of [((t-Bu)ArO) 3tacn)U (III)] with 4,4'-di- tert-butylbenzophenone affords a unique isolable U(IV) ketyl radical species and attempts at isolation were unsuccessful and resulted in methoxide complex from H abstraction and dinuclear para-coupled complex.
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Activation of elemental S, Se and Te with uranium(III): bridging U–E–U (E = S, Se) and diamond-core complexes U–(E)2–U (E = O, S, Se, Te)
TL;DR: In this paper, a trisaryloxide chelating ligand was used to generate the mid-valent U(IV)/(U(IV) dinuclear bis-μ-chalcogenide complexes [Na(DME)3]2[{((AdArO)3N)U}2(μ-O)2] with the diamond-core structural motif.
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Uranium-mediated carbon dioxide activation and functionalization
Oanh P. Lam,Karsten Meyer +1 more
TL;DR: In this article, the authors present accounts of carbon dioxide activation and functionalization mediated by uranium complexes in various oxidation states from low-valent (+3), mid-vialent (+4), to high-valency (+5).