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alpha-Diazo esters are smoothly converted into the corresponding trifluoromethyl thio- or selenoethers by reaction with Me4NSCF3or Me4NSeCF3, respectively, in the presence of catalytic amounts of copper thiocyanate. This straightforward method gives high yields under neutral conditions at room temperature and is applicable to a wide range of functionalized molecules, including diverse alpha-amino acid derivatives. It is well-suited for the late-stage introduction of trifluoromethylthio or -seleno groups into drug-like molecules.

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

 

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The solvothermal reaction of CuSCN with 1,2-bis(diphenylphosphino)ethane (dppe) yielded a coordination polymer, which was characterized to be a complex of CuCN and 1,2-bis(diphenylthiophosphinyl)ethane (dppeS2): [(CuCN)2(dppeS2)]n (1). The identification of complex 1 reveals that CuSCN was decomposed and the sulfur was transferred to dppe, and represents a new example of the transformation of inorganic sulfur to organic sulfur. The weak coordination interactions between CuCN and dppeS 2 indicate that dppeS2 may be substituted by ligands with strong coordination ability. The ligand 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tpt) was chosen as a substitute ligand. Three novel CuCN coordination polymers of tpt were synthesized and characterized: [Cu2(CN) 2(tpt)]n (2) with a 3-D (10,3)-a network, [Cu 2(CN)2(tpt)]n (3) and [Cu2(SCN)(CN) (tpt)]n (4) both with a 2-D (6,3) network, and only complex 2 can be obtained from CuCN directly. Interestingly, compounds 2 and 3 are genuine high-dimensional supramolecular isomers. During the syntheses of 2-4, single crystals of dppeS2 were isolated, which indicates it was substituted by tpt ligand and also confirmed the transformation of sulfur from CuSCN to dppe. The transformation of sulfur can be observed only when the temperature is relative high (>160 C). At 140 C, complex 5 containing only CuSCN was attained and no dppeS2 has been monitored in the resulting filtrate. The Royal Society of Chemistry 2006.

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

 

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Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media. We’ll be discussing some of the latest developments in chemical about CAS: category: copper-catalyst, Name is Copper(I) oxide, belongs to copper-catalyst compound, is a common compound. category: copper-catalystIn an article, authors is , once mentioned the new application about category: copper-catalyst.

Thiazolidinedione derivatives of the formula: STR1 and pharmacologically acceptable salts thereof are novel compounds, which exhibit in mammals blood sugar- and lipid-lowering activity, and are of value as a therapeutic agent for treatment of diabetes and hyperlipemia.

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

 

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Biofilm formation is problematic and hence undesirable in medical and industrial settings. In addition to bacteria, phototrophic organisms are an integral component of biofilms that develop on surfaces immersed in natural waters. 1-Alkyl-3-methyl imidazolium ionic liquids (IL) with varying alkyl chain length were evaluated for their influence on the formation of monospecies (Navicula sp.) and multispecies biofilms under phototrophic conditions. An IL with a long alkyl side chain, 1-hexadecyl-3-methylimidaazolium chloride ([C16(MIM)][Cl]) retarded growth, adhesion and biofilm formation of Navicula sp. at concentrations as low as 5 muM. Interestingly, [C16(MIM)][Cl] was very effective in preventing multispecies phototrophic biofilms on fibre reinforced plastic surfaces immersed in natural waters (fresh and seawater). SYTOX Green staining and chlorophyll leakage assay confirmed that the biocidal activity of the IL was exerted through cell membrane disruption. The data show that [C16(MIM)][Cl] is a potent inhibitor of phototrophic biofilms at micromolar concentrations and a promising agent for biofilm control in re-circulating cooling water systems. This is the first report that ionic liquids inhibit biofilm formation by phototrophic organisms which are important members of biofilms in streams and cooling towers.

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

 

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Copper(I)-catalysed reactions of cis-PtCl2(L)2 (L= PEt3, L2 = dppe, dppp) with buta-1,3-diyne have given the corresponding diynyl complexes, cis-Pt(C?CC?CH)2(L)2 (L= PEt3 1, L2 = dppe 2, dppp 3) whose solid-state structures have been determined from single crystal X-ray diffraction studies. Theoretical calculations were carried out to probe the electronic structure of these diynyl complexes. Complex 2 reacts with Co2(CO)8 to give a bis-adduct 5 and with Ru3(mu-dppm)(CO)10 to give a mono-adduct 6; in both, the least hindered C?C triple bond(s) is(are) coordinated. Lithiation (LiBut) of 2 gives a dilithio derivative, which has been converted to dimethyl 7 or mono-SiMe3 8 or -Au(PPh3) 9 complexes. Cu(I) and Ag(I) (MI) adducts (quot;tweezerquot; complexes) have been obtained from reactions of 2 with MISCN or [MI(NCMe)4]+. An ES mass spectrometric study of the interactions of 2 with Group 1 cations and with Tl+ is also described; comparative experiments with {W(CO)3Cp}2(mu-C8), in which the four C?C triple bonds do not have a “tweezer” conformation, have also been carried out. The degree of association is determined by the competitive solvation of the Group 1 cation. Coupling of the buta-1,3-diynyl complexes with Pt(OTf)2(L?)2 gives homo- or mixed-ligand molecular squares cyclo-{(L)2Pt(mu-C?CC?C)2Pt(L?) 2}2 (L, L? = PEt3, L2, L?2 = dppe, dppp; not all combinations), of which the molecular structure of cyclo-{Pt(mu-C?CC?C)(dppe)}4 17 is described (as solvates containing dmso). The molecular squares form adducts with substituted ammonium triflates [NH2R2][OTf] (R = Et, Pri, Cy; NH2R2 = dbuH) and with Group 11 cations [MI(NCMe)]+.

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

 

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The development of new antifouling coatings with respect to the marine environment is actually crucial. The aim of the present work is to concept an erodible paint formulated with biodegradable polyester as binders and which combines two modes of prevention: chemical and physical repelling of biofouling. This system is principally dedicated to disturb durable settlement of microfouling. Each component was chosen according to its specific properties: chlorhexidine is a bisdiguanide antiseptic with antibacterial activity, zinc peroxide is an inorganic precursor of high instable entities which react with seawater to create hydrogen peroxide, Tween 85 is a non ionic surfactant disturbing interactions between colonizing organisms and surface. Obtained results highlighted the interest on mixing such molecules to obtain a promising coating with lower toxicity than traditional systems.

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

 

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Analytical procedures based on ion chromatography utilising an anion exchange column and UV detection are described for the quantification of thiosulfate, polythionates and gold thiosulfate both in leach solutions and adsorbed on anion exchange resins. The analysis of resins involves a two step perchlorate strip, and since perchlorate is used as the chromatography eluent, the high background concentration in the sample has little effect on the retention. Results are reported for the analysis of gold thiosulfate leach solutions and it is shown that tetrathionate and pentathionate are the dominant reaction products from thiosulfate oxidation at pH 8.5 and 9, whilst trithionate and sulfate are formed at pH 10.4. An increase in thiosulfate consumption when increasing pH from 8.5 to 9 is attributed to the increase in the rate of copper(I) oxidation with increasing ammonia concentration. However, the rate of thiosulfate consumption is higher at pH 9.0 than pH 10.4, and this is explained in terms of the differing reaction products. The adsorption of thiosulfate, polythionates and gold thiosulfate onto anion exchange resins is also discussed with reference to the quantification of the equilibrium solution and resin concentration of each species. Isotherms for gold on resin vs. gold in solution are reported for solutions of various polythionate concentrations.

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

 

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Thermal microgravimetry, mass spectrometry, and X-ray diffractometry were used to investigate the ability of NO2 to oxidize copper.NO2 oxidizes a copper plate with formation of oxide film consisting of Cu2O (predominant) and CuO.The oxidation obeys a cubic law, and proceeds faster than in oxygen.An oxidation mechanism is presented on the basis of kinetic and structural data.

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

 

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The solvothermal reactions of CuX (X = CN, SCN) with Cu(pyzca)2 (pyzca = pyrazine-2-carboxylate) afforded compounds Cu2(CN)(pyzca) (1) and CuI (SCN) Cu0.5II (pyzca) (2), respectively. They are both characterized by infrared spectroscopy, elemental analysis and X-ray single-crystal analysis. The structure of 1 exhibits a (728)2(7383) network which has not been reported for the (3, 4)-connected nets, while that of 2 displays a (63)(658) network which belongs to the ins topology.

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

 

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Thermal decomposition of Bi(SCN)3, Cd(SCN)2, Pb(SCN)2 and Cu(SCN)2 has been studied. The thermal analysis curves and the diffraction patterns of the solid intermediate and final products of the pyrolysis are presented. The gaseous products of the decomposition (SO2 and CO2) were detected and quantitatively determined. Thermal, X-ray and chemical analyses have been used to establish the nature of the reactions occurring at each stage in the decomposition.

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