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Cubane pyridine-acetylacetonate cluster complexes with the M3CuS

The reactions between [Mo3(mu3-S)(mu2- S)3(Acac)3(Py)3]PF6 (HAcac is acetylacetone, Py is pyridine) and CuX (X = Cl, I, SCN) afford heterometallic cubane clusters [Mo3(CuX)(mu3-S)4(Acac) 3(Py)3]PF6. The structures of two new compounds, [Mo3(CuCl)S4(Acac)3(Py) 3]PF6 ? 3.25CH2Cl2 ? 0.5C6H5CH3 and [Mo3(CuI)S 4(Acac)3(Py)3]PF6 ? 4C 6H6, are determined by X-ray diffraction analysis. All synthesized compounds are characterized by elemental analysis and IR spectra. According to the vibrational spectra, the thiocyanate complex in the solid state is a mixture of the bond isomers [Mo3(CuNCS)S4(Acac) 3(Py)3]PF6 and [Mo3(CuSCN)S 4(Acac)3(Py)3]PF6, whereas in solution this complex exists as a isothiocyanate form.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Stabilizing CuPd Nanoparticles via CuPd Coupling to WO2.72 Nanorods in Electrochemical Oxidation of Formic Acid

Stabilizing a 3d-transition metal component M from an MPd alloy structure in an acidic environment is key to the enhancement of MPd catalysis for various reactions. Here we demonstrate a strategy to stabilize Cu in 5 nm CuPd nanoparticles (NPs) by coupling the CuPd NPs with perovskite-type WO2.72 nanorods (NRs). The CuPd NPs are prepared by controlled diffusion of Cu into Pd NPs, and the coupled CuPd/WO2.72 are synthesized by growing WO2.72 NRs in the presence of CuPd NPs. The CuPd/WO2.72 can stabilize Cu in 0.1 M HClO4 solution and, as a result, they show Cu, Pd composition dependent activity for the electrochemical oxidation of formic acid in 0.1 M HClO4 + 0.1 M HCOOH. Among three different CuPd/WO2.72 studied, the Cu48Pd52/WO2.72 is the most efficient catalyst, with its mass activity reaching 2086 mA/mgPd in a broad potential range of 0.40 to 0.80 V (vs RHE) and staying at this value after the 12 h chronoamperometry test at 0.40 V. The synthesis can be extended to obtain other MPd/WO2.72 (M = Fe, Co, Ni), making it possible to study MPd-WO2.72 interactions and MPd stabilization on enhancing MPd catalysis for various chemical reactions.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Extracurricular laboratory:new discovery of Cuprous thiocyanate

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! Read on for other articles about Related Products of 1111-67-7!, Synthetic Route of 1111-67-7

Synthetic Route of 1111-67-7, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 1111-67-7, molcular formula is CCuNS, introducing its new discovery.

Thiolate layers on metal sulfides characterised by XPS, ToF-SIMS and NEXAFS spectroscopy

Surface spectroscopic characterisation of some Cu and Ag thiolate multilayers on metal and metal sulfide substrates was undertaken to establish unequivocally the composition and possible orientation of the multilayer species. This information was sought to attempt to explain the undiminished floatability of sulfide minerals observed for collector coverage exceeding a monolayer. The thiol collectors investigated were dithiophosphate and 2-mercaptobenzothiazole (MBT), and bulk CuMBT and AgMBT complexes were prepared for comparison with the corresponding multilayers. Surface optimised synchrotron X-ray photoelectron spectra and partial electron yield near-edge X-ray absorption fine structure (NEXAFS) spectra confirmed that the Cu dithiolate, detected by secondary ion mass spectroscopy (SIMS), was no more than a minor constituent of the corresponding multilayer. The photoelectron spectra for multilayer CuMBT and AgMBT were similar to those for the corresponding bulk complexes. NEXAFS spectroscopy detected some CuII in bulk CuMBT prepared from cupric ions but not cuprous. The SIMS data were consistent with multilayer patches or islands on top of a chemisorbed monolayer and hence continued exposure of the monolayer in the presence of the multilayer. For each multilayer investigated, the SIMS data provided no evidence to support a multinuclear cluster structure as is present in the corresponding bulk thiolate, but nor could they exclude such a possibility. Angle-dependent NEXAFS spectroscopy at the N K-edge confirmed that MBT monolayers were aligned and revealed that the metal thiolate multilayer was not aligned relative to the substrate, but might nevertheless have been ordered in a cluster structure. It was surmised that undiminished floatability of sulfide minerals with multilayer collector coverage could probably be attributed to the patch-wise nature of the multilayer.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Accurate thermodynamic modeling of ionic liquids/metal salt mixtures: Application to carbon monoxide reactive absorption

For the first time, a theoretical semipredictive approach based on the soft-Statistical Associating Fluid Theory equation of state is presented to model the complexation reaction between carbon monoxide (CO) in a combined ionic liquid (IL) plus a copper(I) metallic salt media in terms of the gas solubility as a function of temperature, pressure, and composition. Two different degrees of molecular approximation are tested. In the first approach, the IL-metal salt mixture is treated as a single compound whose parameters are modified according to the concentration of the metallic salt. In the second approach, both compounds are treated as independent species, enhancing the predictive capability of the model. The complexation between CO molecules and the metal salt is reproduced by adding specific cross-association interaction sites that simulate the reaction. The density of the doped IL and the CO solubility are described in quantitative agreement with the experimental data at different operating conditions.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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A facile deposition method for CuSCN: Exploring the influence of CuSCN on J-V hysteresis in planar perovskite solar cells

Inorganic hole?transporting materials (HTMs) are a promising class of compounds for improving the long-term stability of perovskite solar cells. In this study, copper(I) thiocyanate (CuSCN) has been applied as an HTM in planar-structured thin film perovskite solar cells based on methylammonium lead(II) triiodide. A common obstacle associated with the deposition of inorganic HTMs in perovskite-based solar cell devices is the damaging effect of polar solvents, required during the solution-processed deposition step, on the underlying perovskite film. Here we describe a novel fabrication method that allows the deposition of a CuCSN layer on perovskite film, achieving a maximum power conversion efficiency of 9.6%. The magnitude of J-V hysteresis is found to be strongly dependent on the HTM used, with the phenomenon being much more prevalent in the CuSCN- and spiro-OMeTAD-based devices compared to CuI-based devices. Interestingly, CuSCN and CuI showed significantly different J-V hysteresis behaviors despite their similar physicochemical properties. Further characterization by open circuit voltage decay (OCVD) measurements revealed that the relaxation of the perovskite polarization depends on the light intensity and the adjacent HTM layer. We propose that the stronger J-V hysteresis in CuSCN compared to CuI is a result of defects generated during the deposition process and possible degradation at the material interfaces while other possibilities are also discussed.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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An IrRu alloy nanocactus on Cu2-xS@IrSy as a highly efficient bifunctional electrocatalyst toward overall water splitting in acidic electrolytes

Development of highly active and durable bifunctional electrocatalysts for overall water splitting is vital for the economical production of H2 as an alternative energy source. Herein, we report the synthesis of Cu2-xS@IrSy@IrRu nanoparticles (CIS@IrRu NPs), which show excellent catalytic performances for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in an acidic electrolyte. Benefiting from the optimal composition of IrRu and the stable IrSy shell, the cactus-like IrRu NPs show high electrocatalytic activity and stability. The cactus-like IrRu NPs exhibit optimal HER and OER performances and high stability at a ratio of Ir/Ru 1.00:1.07. In overall water splitting, the CIS@Ir48Ru52 NPs achieve a current density of 10 mA cm-2 at a cell voltage of only 1.47 V in 0.1 M HClO4 electrolyte and show negligible degradation after 100 h of continuous operation in the stability test.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Can You Really Do Chemisty Experiments About Copper(I) oxide

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Process for the preparation of hydroxybiphenyls

A process for the production of a hydroxybiphenyl by the hydrolysis of a bromobiphenyl, at a temperature below 300 C., in the presence of both a copper-based catalyst and a separate cocatalyst selected from amongst halides, phosphates, nitrates, alcoholates, silicates, alcohols, carboxylic acids, sulfonic acids, organic sulfur-containing compounds, carbon monoxide, quinolines, tertiary amines, ammoniums, phosphines, phosphoniums, cyanides and palladium.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Ultraflexible and High-Performance Multilayer Transparent Electrode Based on ZnO/Ag/CuSCN

Driven by huge demand for flexible optoelectronic devices, high-performance flexible transparent electrodes are continuously sought. In this work, a flexible multilayer transparent electrode with the structure of ZnO/Ag/CuSCN (ZAC) is engineered, featuring inorganic solution-processed cuprous thiocyanate (CuSCN) as a hole-transport antireflection coating. The ZAC electrode exhibits an average transmittance of 94% (discounting the substrate) in the visible range, a sheet resistance (Rsh) of 9.7 Omega/sq, a high mechanical flexibility without Rsh variation after bending 10 000 times, a long-term stability of 400 days in ambient environment, and a scalable fabrication process. Moreover, spontaneously formed nanobulges are integrated into ZAC electrode, and light outcoupling is significantly improved. As a result, when applied into super yellow-based flexible organic light-emitting diode, the ZAC electrode provides a high-current efficiency of 23.4 cd/A and excellent device flexibility. These results suggest that multilayer thin films with ingenious material design and engineering can serve as a promising flexible transparent electrode for optoelectronic applications.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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A coordination polymer based on twofold interpenetrating three-dimensional four-connected nets of 42638 topology, [CuSCN(bpa)] [bpa = 1,2-bis(4-pyridyl)ethane]

The novel coordination polymer [CuSCN(bpa)] [bpa= 1,2-bis(4-pyridyl)ethane] consists of two interpenetrating three-dimensional four-connected frameworks of rare 42638 topology, each being constructed from the cross-linkage of infinite zigzag [CCuSCN)2](?) chains by bpa ligands.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Quinoline derivatives

The invention has an object to provide a novel quinoline derivative of the following formula (I) which has no benzyl group in the 5-position and shows hypoglycemic effect, particularly, by oral administration: STR1 in which R1 is hydrogen; an alkyl group of 1-6 carbon atoms, an amino group of the formula of –NR4 R5 in which each of R4 and R5 independently is hydrogen, alkyl of 1-6 carbon atoms, phenyl, pyridyl, pyrimidyl or benzoyl; or a phenyl group, a naphthyl group, a cycloalkyl group having 3 to 8 carbon atoms, or a 5 to 8 membered heterocyclic group comprising, as ring-constituting atoms, 1 to 2 nitrogens, oxygens or sulfurs and remaining carbon atoms, each of which may have, as a substituent, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, halogen, hydroxyl, halogenoalkyl of 1-6 carbon atoms, halogenoalkoxy of 1-6 carbon atoms, nitro, amino, phenyl, thienyl, furyl, thiazolyl or pyridyl; Z is O, S, C=O, or CH2 ; E is S or O; m is an integer of 0 to 4; p is an integer of 0 to 4; q is an integer of 0 to 4; and the double line composed of a broken line and a solid line means a single or double bond.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”