The X-ray structures and spectroscopic and magnetic properties of [tetrakis(&mgr;-1-phenylcyclopropane-1-carboxylato-O,O')bis(ethanol-O)dicopper(II)], 1, and catena-poly[[bis(&mgr;-diphenylacetato-O:O')dicopper](&mgr;(3)-diphenylacetato-1-O:2-O':1'-O')(&mgr;(3)-diphenylacetato-1-O:2-O':2'-O')], 2, two extended-chain copper(II) carboxylates with dinuclear paddle-wheel subunits, are reported. 1 crystallizes in the triclinic space group P&onemacr;, with a = 6.8873(3) Å, b = 11.7367(6) Å, c = 13.7899(7) Å, alpha = 107.076(4) degrees, beta = 93.545(4) degrees, gamma = 103.967(4) degrees, Z = 1. The Cu.Cu distance is 2.6009(4) Å, and the Cu.carboxylate O distances are in the range 1.937(2)-1.962(2) Å. The ethanol at the apex forms an unsymmetrical bifurcated H bond to two carboxylate oxygens of another dinuclear unit with O.O distances 2.980(3) and 3.108(3) Å, thereby extending the structure along the a-axis. The magnetic structure consists of isolated antiferromagnetically coupled dinuclear copper units, with a -2J value of 242 cm(-)(1), in concurrence with the EPR parameters, viz., g(x)() = 2.03(1), g(y)() = 2.07(1), g(z)() = 2.35(1), A( parallel) = 0.064(2) cm(-)(1), D = 0.316(15) cm(-)(1), E = 0.005(1) cm(-)(1). The -2J value is the smallest value measured for dinuclear copper carboxylates with oxygen-donor ligands at the axial position and no electron-withdrawing carboxylate R groups. 2 crystallizes in the monoclinic space group P2(1)/c, with a = 15.953(2) Å, b = 5.385(6) Å, c = 28.322(10) Å, beta = 120.22(3) degrees, Z = 2. The compound contains tetrakis(diphenylacetato)dicopper(II) units, forming a polymeric structure along the b-axis by axial coordination of a carboxylate oxygen to copper of a subsequent dinuclear unit, at 2.323(11) Å. The intradimer Cu.Cu distance is 2.594(4) Å; the interdimer Cu.Cu distance is 3.425(5) Å. The -2J value of 321 cm(-)(1) was interpreted as originated from isolated antiferromagnetically coupled dinuclear copper units. The EPR parameters are g(x)() = 2.07(1), g(y)() = 2.02(1), g(z)() = 2.33(1), D = 0.347(10) cm(-)(1), E = 0.0034(5) cm(-)(1). The dinuclear subunits are likely candidates for the catalytically active Cu species in copper(II)-catalyzed oxidation of carboxylic acids.
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http://dx.doi.org/10.1021/ic9614733 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Shenzhen Geim Graphene Center, Shenzhen Key Laboratory of Advanced Layered Materials for Value-added Applications, Tsinghua-Berkeley Shenzhen Institute and Institute of Materials Research, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, PR China.
The electrochemical reduction of CO to CH is promising for carbon neutrality and renewable energy storage but confronts low CH selectivity, especially at high current densities. The key challenge lies in promoting *CO intermediate and *H coupling while minimizing side reactions including C-C coupling and H-H coupling, which is particularly difficult at high current density due to abundant intermediates. Here we report a cooperative strategy to address this challenge using Cu-based catalysts comprising Cu-N coordination polymer and CuO component that can simultaneously manage the key intermediates *CO and *H.
View Article and Find Full Text PDFActa Crystallogr B Struct Sci Cryst Eng Mater
December 2024
School of Chemistry, University College Dublin, Belfield, Dublin 4, D04 N2E5, Ireland.
Hydrothermal synthesis led to four novel 3D pillared-layer metal-organic frameworks: [Cu(4,4'-bipy)(MoO)·0.3HO] (1), [Cu(4,4'-bipy)(MoO)·0.25HO] (2), [Cu(4,4'-bipy)(MoO)·0.
View Article and Find Full Text PDFSmall
November 2024
MIIT Key Laboratory of Thermal Control of Electronic Equipment, School of Energy and Power Engineering, School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.
To address the bottle-neck carbon-carbon coupling issue during electrochemical carbon dioxide reduction (eCORR) to multicarbon (C) products, this work develops an anion-directed strategy (Cl, NO , and SO ) to regulate interatomic distance of Cu diatoms. In comparison to pristine Cu (with a typical Cu-Cu distance of 2.53 Å), Cu-boroimidazole frameworks (BIF)/SO, NO, and Cl material shows elongated diatomic distance of 3.
View Article and Find Full Text PDFChemistryOpen
December 2024
Department of Chemistry, Technical University of Denmark,Building 207, Kemitorvet, DK-2800 Kgs., Lyngby, Denmark.
Multicentre redox metalloproteins undergo conformational changes on electrochemical surfaces, or on enzyme substrate binding. The two-centre copper enzymes, laccase (Type I and TypeII/III Cu) and nitrite reductase (CuNIR) (Type I and Type II Cu) are examples. With some exceptions, these enzymes show no non-turnover voltammetry on Au(111)-surfaces modified by thiol based self-assembled molecular monolayers, but dioxygen or nitrite substrate triggers strong electrocatalytic signals.
View Article and Find Full Text PDFPhys Chem Chem Phys
November 2024
Institute of Fundamental Physics (AbinitSim Unit, ABINITFOT Group), Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
The concept of fluxionality has been invoked to explain the enhanced catalytic properties of atomically precise metal clusters of subnanometer size. Cu isolated in the gas phase is a classical case of a fluxional metal cluster where a conical intersection leads to a Jahn-Teller (JT) distortion resulting in a potential energy landscape with close-lying multiminima and, ultimately, fluxional behavior. In spite of the role of conical intersections in the (photo)stability and (photo)catalytic properties of surface-supported atomic metal clusters, they have been largely unexplored.
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