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A coating composition comprising a rosin compound, a polymer containing organosilyl ester groups, and an antifoulant as essential components is disclosed. This rosin-based coating composition gives a coating film which forms no residue layer on the surface thereof over long-term immersion, is hence free from physical defects such as cracks and peeling and capable of maintaining a sufficiently high rate of film erosion and preventing the attachment of marine organisms over a long period of time has satisfactory suitability for recoating, and has the satisfactory ability to prevent marine-organism attachment over the out-fitting period.

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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 power conversion efficiency of perovskite solar cells (PSCs) has been certified as ?22.1%, approaching the best single crystalline silicon solar cells. The improvement in the performance of PSCs could be achieved through the testing of novel materials in the device. This review briefly discusses the systematic introduction about several inorganic and organic electron-transporting materials (ETMs) and hole-transporting materials (HTMs) for efficient PSCs. The transport mechanism of electrons and holes in different ETMs/HTMs is also discussed on the basis of energy band diagrams with respect to the perovskite absorber. Moreover, the introduction of appropriate interfacial materials, hybrid ETMs, and doping is discussed to optimize the interfacial electronic properties between the perovskite layer and the charge-collecting electrode.

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

 

Our Top Choice Compound: Cu2O

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The invention concerns a heterocyclene derivative of the formula I wherein Ar1 is optionally substituted phenyl, naphthyl or a 9- or 10-membered bicyclic heterocyclic moiety; A1 is a direct link to X1 or (1-3C)alkylene; X1 is oxy, thio, sulphinyl, sulphonyl or imino; Ar2 is optionally substituted 5-membered heterocyclene moiety; R1 is (1-4C)alkyl, (3-4C)alkenyl or (3-4C)alkynyl; and R2 and R3 together form a group of the formula -A2-X2-A3- which, together with the carbon atom to which A2 and A3 are attached, defines a ring having 5 to 7 ring atoms, wherein each of A2 and A3 is (1-3C)alkylene and X2 is oxy, thio, sulphinyl or sulphonyl; or a pharmaceutically-acceptable salt thereof. The compounds of the invention are inhibitors of the enzyme 5-lipoxygenase

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

 

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A stereoselective [5+2] cycloaddition reaction using a new five-carbon unit, that has a dicobalt acetylene complex moiety and an enol silyl ether moiety, was developed. In the presence of a Lewis acid, the five-carbon unit reacted with an enol triisopropylsilyl ether to give a 1-acetyl-2- silyoxycycloheptane derivative, in which the three contiguous substituents on the seven-membered ring arrange cis to each other.

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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 magnetic properties of chalcogenide spinel CuCr2Se4 nanocrystals have been studied as a function of crystallite size (15-30 nm). A solution-based method is used for the facile synthesis of the nanocrystals with good size control. They have close to cubic morphology with a narrow size distribution and exhibit superparamagnetic behavior at room temperature. The Curie temperature and saturation magnetization of the nanocrystals are lower as compared with the bulk and decrease with decreasing nanocrystal size. A similar trend is observed in the paramagnetic state for the Curie-Weiss temperature and effective magnetic moment. The low temperature magnetization behavior can be qualitatively explained by spin glass dynamics.

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

 

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A triply-interpenetrating diamondoid coordination polymer [Cu 4(SCN)4(tpom)]·2H2O (1, tpom = tetrakis(4-pyridyloxymethylene)methane) was prepared, which is built from an unprecedented pseudohalide cubane cluster Cu4(SCN)4 and tetrahedral tpom ligand. 1 exhibits high thermal stability and temperature-dependent photoluminescence behaviors resembling those of Cu 4Cl4 complexes.

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

 

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(Hetero)aryl, benzylic, and alkyl zinc halides were thiolated with N-thiophthalimides at 25 C within 1 h in the presence of 5?10 % Cu(OAc)2?H2O to furnish the corresponding polyfunctionalized thioethers in good yields. This electrophilic thiolation was extended to the introduction of trifluoromethylthio (SCF3), thiocyanate (SCN), and selenophenyl (SePh) groups. The utility of this method was shown in a seven-step synthesis of a potent cathepsin D inhibitor in 34 % overall yield.

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

 

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Charge-selective disordered hetero-junctions were formed in evaporated In2S3 layers by diffusing at 200 C CuI from a CuSCN source. The thicknesses of In2S3 layers and diffusion times were varied between 5 and 80 nm and between 2 and 19 min, respectively. In some cases CuSCN layers were etched back with pyridine. Spectral and time-dependent surface photovoltage measurements were carried out in the capacitor arrangement. It was observed that a competing process of charge separation and relaxation was initiated together with the formation of the charge-selective In2S3/In2S3:Cu hetero-junction. Modulated SPV amplitude for different annealing times and thicknesses of the evaporated In2S3 layers. Copyright

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

 

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In the presence of phosphine chalcogenoniobates such as Li3[NbS4] · 4 CH3CN (I), (NEt4)4[Nb6S17] · 3 CH3CN (II) and (NEt4)2[NbE?3(EBu)] (IIIa: E? = E = S; IIIb: E = Se, E? = S; III c: E = E? = Se) respectively react with copper and gold salts to give a number of new heterobimetallic niobium copper(gold) chalcogenide clusters. These clusters show metal chalcogenide units already known from the complex chemistry of the tetrachalcogenometalates [ME4]n- (M = V, n = 3, E = S; M = Mo, W, n = 2, E = S, Se). The compounds 1-8 owe a central tetrahedral [NbE4] structural unit, which coordinates eta2 from two to five coinage metal atoms, employing the chalcogenide atoms of the [NbE4] edges. The compounds 9-11 have a [M?2Nb2E4] (M? = Cu, Au) heterocubane unit in common, involving a metal metal bond between the niobium atoms, while the compounds 12 and 13 show a complete and 14 an incomplete [M?3NbE3X] heterocubane structure (X = Cl, Br). 15 consists of a Cu6Nb2 cube with the six planes capped by mu4 bridging selenide ligands forming an octahedra. The compounds 1-15 are listed below: (NEt4)?1[Cu2NbSe 2S2(dppe)2] · 2 DMF (1), [Cu3NbS4(PPh3)4] (2), [Au3NbSe4(PPh3)4] · Et2O (3), [Cu4NbS4Cl(PCy3)4] (4), [Cu4NbS4Cl(PBu3)4] · 0,5 DMF (5), [Cu4NbSe4(NCS)(PBu3)4] · DMF (6), [Cu4NbS4(NCS)(dppm)4] · Et2O (7), [Cu5NbSe4Cl2(dppm)4] · 3 DMF (8), [Cu2Nb2S4Cl2(PMe3) 6] · DMF (9), [Au2Nb2Se4Cl2(PMe3) 6] · DMF (10), (NEt4)2[Cu3Nb2S 4(NCS)5(dppm)2(dmf)] · 4 DMF (11), [Cu3NbS3Br(PPh3)3(dmf) 3]Br · [CuBr(PPh3)3] · PPh3 · OPPh3 · 3 DMF (12), [Cu3NbS3Cl2(PPh3) 3(dmf)2] · 1.5 DMF (13), (NEt4)[Cu3NbSe3Cl3(dmf)3] (14), [Cu6Nb2Se6O2(PMe3) 6] (15). The structures of these compounds were obtained by X-ray single crystal structure analysis. WILEY-VCH Verlag GmbH, D-69451 Weinheim, 2001.

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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 properties recently reported on the Cu(I)-iodide pyrimidine nonporous 1D-coordination polymer [CuI(ANP)]n (ANP = 2-amino-5-nitropyridine) showing reversible physically and chemically driven electrical response have prompted us to carry a comparative study with the series of [CuX(ANP)]n (X = Cl (1), X = Br (2), X = CN (4), and X = SCN (5)) in order to understand the potential influence of the halide and pseudohalide bridging ligands on the physical properties and their electrical response to vapors of these materials. The structural characterization of the series shows a common feature, the presence of -X-Cu(ANP)-X- (X = Cl, Br, I, SCN) double chain structure. Complex [Cu(ANP)(CN)]n (4) presents a helical single chain. Additionally, the chains show supramolecular interlinked interactions via hydrogen bonding giving rise to the formation of extended networks. Their luminescent and electrical properties have been studied. The results obtained have been correlated with structural changes. Furthermore, the experimental and theoretical results have been compared using the density functional theory (DFT). The electrical response of the materials has been evaluated in the presence of vapors of diethyl ether, dimethyl methylphosphonate (DMMP), CH2Cl2, HAcO, MeOH, and EtOH, to build up simple prototype devices for gas detectors. Selectivity toward gases consisting of molecules with H-bonding donor or acceptor groups is clearly observed. This selective molecular recognition is likely due to the 2-amino-5-nitropyridine terminal ligand.

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