A Dicopper Platform that Stabilizes the Formation of Pentanuclear Coinage Metal Hydride Complexes
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[1] M. Lutz,et al. Cooperative H2 Activation on Dicopper(I) Facilitated by Reversible Dearomatization of an “Expanded PNNP Pincer” Ligand , 2019, Chemistry.
[2] Takayuki Nakajima,et al. Synergistic Cu2 Catalysts for Formic Acid Dehydrogenation. , 2019, Journal of the American Chemical Society.
[3] S. Buchwald,et al. CuH-Catalyzed Enantioselective Ketone Allylation with 1,3-Dienes: Scope, Mechanism, and Applications. , 2018, Journal of the American Chemical Society.
[4] Daniel S. Levine,et al. Dicopper Alkyl Complexes: Synthesis, Structure, and Unexpected Persistence , 2018, Organometallics.
[5] R. O'hair,et al. How to Translate the [LCu2(H)]+‐Catalysed Selective Decomposition of Formic Acid into H2 and CO2 from the Gas Phase into a Zeolite. , 2018 .
[6] A. White,et al. Selective Reduction of CO2 to a Formate Equivalent with Heterobimetallic Gold- - -Copper Hydride Complexes. , 2017, Angewandte Chemie.
[7] B. Kure,et al. A Fluxional Cu8 H6 Cluster Supported by Bis(diphenylphosphino)methane and its Facile Reaction with CO2. , 2017, Chemistry.
[8] D. Paley,et al. Cationic Copper Hydride Clusters Arising from Oxidation of (Ph3P)6Cu6H6. , 2017, Journal of the American Chemical Society.
[9] Micah S. Ziegler,et al. Dicopper Cu(I)Cu(I) and Cu(I)Cu(II) Complexes in Copper-Catalyzed Azide-Alkyne Cycloaddition. , 2017, Journal of the American Chemical Society.
[10] P. Dugourd,et al. Selectivity Effects in Bimetallic Catalysis: Role of the Metal Sites in the Decomposition of Formic Acid into H2 and CO2 by the Coinage Metal Binuclear Complexes [dppmMM′(H)]+ , 2017 .
[11] G. Bertrand,et al. Spectroscopic Evidence for a Monomeric Copper(I) Hydride and Crystallographic Characterization of a Monomeric Silver(I) Hydride. , 2017, Angewandte Chemie.
[12] G. Reid,et al. Synthesis, Structural Characterization, and Gas-Phase Unimolecular Reactivity of Bis(diphenylphosphino)amino Copper Hydride Nanoclusters [Cu3(X)(μ3-H)((PPh2)2NH)3](BF4), Where X = μ2-Cl and μ3-BH4. , 2016, Inorganic chemistry.
[13] T. Cundari,et al. A Dinitrogen Dicopper(I) Complex via a Mixed-Valence Dicopper Hydride. , 2016, Angewandte Chemie.
[14] C. Philouze,et al. Room-Temperature Characterization of a Mixed-Valent μ-Hydroxodicopper(II,III) Complex. , 2016, Inorganic chemistry.
[15] G. Lalic,et al. Coinage Metal Hydrides: Synthesis, Characterization, and Reactivity. , 2016, Chemical reviews.
[16] Daniel S. Levine,et al. Aryl Group Transfer from Tetraarylborato Anions to an Electrophilic Dicopper(I) Center and Mixed-Valence μ-Aryl Dicopper(I,II) Complexes. , 2016, Journal of the American Chemical Society.
[17] W. E. van Zyl,et al. Polyhydrido Copper Clusters: Synthetic Advances, Structural Diversity, and Nanocluster-to-Nanoparticle Conversion. , 2016, Accounts of chemical research.
[18] M. Chiang,et al. Diselenophosphate-Induced Conversion of an Achiral [Cu20H11{S2P(OiPr)2}9] into a Chiral [Cu20H11{Se2P(OiPr)2}9] Polyhydrido Nanocluster. , 2015, Angewandte Chemie.
[19] B. Kure,et al. Facile insertion of carbon dioxide into Cu₂(μ-H) dinuclear units supported by tetraphosphine ligands. , 2014, Chemistry, an Asian journal.
[20] J. Bacsa,et al. Bonding and reactivity of a μ-hydrido dicopper cation. , 2013, Angewandte Chemie.
[21] J. Norton,et al. Electron transfer from hexameric copper hydrides. , 2013, Journal of the American Chemical Society.
[22] B. Lipshutz,et al. Asymmetric CuH-catalyzed hydrosilylations en route to the C-9 epimer of amphidinoketide iota. , 2007, Organic letters.
[23] Martin Oestreich,et al. Vom Schleifen eines “Rohdiamanten”: die “Cu-H”-Katalyse mit Silanen , 2007 .
[24] M. Oestreich,et al. Polishing a diamond in the rough: "Cu--H" catalysis with silanes. , 2007, Angewandte Chemie.
[25] B. Lipshutz,et al. CuH in a bottle: a convenient reagent for asymmetric hydrosilylations. , 2005, Angewandte Chemie.
[26] N. Mankad,et al. Synthesis, Structure, and Alkyne Reactivity of a Dimeric (Carbene)copper(I) Hydride , 2004 .
[27] S. Buchwald,et al. Copper-catalyzed asymmetric conjugate reduction as a route to novel beta-azaheterocyclic acid derivatives. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[28] B. Lipshutz,et al. Asymmetric hydrosilylation of aryl ketones catalyzed by copper hydride complexed by nonracemic biphenyl bis-phosphine ligands. , 2003, Journal of the American Chemical Society.
[29] M. R. McLean,et al. Neutron diffraction structure analysis of a hexanuclear copper hydrido complex, H6Cu6[P(p-tolyl)3]6: an unexpected finding , 1989 .
[30] C. Raston,et al. Lewis-Base Adducts of Group 11 Metal(I) Compounds. 49. Structural Characterization of hexameric and pentameric (triphenylphosphine)copper(I) hydrides , 1989 .
[31] J. Stryker,et al. Selective hydride-mediated conjugate reduction of .alpha.,.beta.-unsaturated carbonyl compounds using [(Ph3P)CuH]6 , 1988 .
[32] G. Doyle,et al. Mixed copper/iron clusters. The preparation and structure of the large planar cluster anions, Cu3Fe3(CO)123- and Cu5Fe4(CO)163-. , 1986, Journal of the American Chemical Society.