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Vanadium catalysts were successfully used to oxidize benzene in two-phase reaction system under Udenfriend-like conditions. The selectivity of the reaction changed completely as a function of the type of reducing agents. Relatively high turnover numbers were obtained as the reductant/V molar ratio increased. High selectivity to phenol production was achieved by using ascorbate as reducing agent, while the use of a different reductant (dithiocompounds) changed completely the selectivity toward more oxidized products, i.e., hydroquinone. Thioreducing agents favored the oxidation of the aromatic ring of benzene, while ascorbate selectively favored the introduction of only one oxygen. The exploitation of the reducing capacity of the system was remarkable. The reaction yield depended on the amount of ascorbate present or, more precisely, upon the ascorbate/V molar ratio. Vanadyl concentrations tended to slowly decrease as the benzene oxidation reaction rate increased, generating VVions.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.10049-08-8, Name is Ruthenium(III) chloride, molecular formula is Cl3Ru. In a Article,once mentioned of 10049-08-8, Computed Properties of Cl3Ru

Photoelectrochemical studies of RuS2-coated TiO2 electrodes showed semiconductor sensitization by RuS2 fine particles on TiO2.RuS2 particles of ca. 100 nm size were observed from a scanning electron micrograph of the RuS2/TiO2 electrode surface.RuS2-coated TiO2 electrodes showed continuous wide absorption in the visible spectral region.Photoelectrochemical measurements of several RuS2/TiO2 electrodes, prepared under different conditions, were carried out.The electron-transfer efficiency from RuS2 to TiO2 was affected by the number of RuS2 colloid coatings and the preparation temperature of the RuS2 colloids.A schematic study was carried out on the effect of a heat treatment in order to find the optimum temperature for the maximum sensitization efficiency.A comparison of the absorption of the absorption and action spectra of the RuS2/TiO2 electrode showed that only small RuS2 particles with a critical size distribution could transfer the photo-generated electrons to TiO2.A band-gap value of ca. 2.8 eV was evaluated (from the photocurrent action spectrum) for the RuS2 particles with high sensitization efficiency.A scheme which shows the energy diagram for RuS2 fine particles has been proposed by considering the flat-band potential values derived from the photocurrent onset potentials and the above-mentioned band-gap value.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Carbohydrates are integral to biological signaling networks and cell-cell interactions, yet the detection of discrete carbohydrate-lectin interactions remains difficult since binding is generally weak. A strategy to overcome this problem is to create multivalent sensors, where the avidity rather than the affinity of the interaction is important. Here we describe the development of a series of multivalent sensors that self-assemble via hydrophobic supramolecular interactions. The multivalent sensors are comprised of a fluorescent ruthenium(II) core surrounded by a heptamannosylated beta-cyclodextrin scaffold. Two additional series of complexes were synthesized as proof-of-principle for supramolecular self-assembly, the fluorescent core alone and the core plus beta-cyclodextrin. Spectroscopic analyses confirmed that the three mannosylated sensors displayed 14, 28, and 42 sugar units, respectively. Each complex adopted original and unique spatial arrangements. The sensors were used to investigate the influence of carbohydrate spatial arrangement and clustering on the mechanistic and qualitative properties of lectin binding. Simple visualization of binding between a fluorescent, multivalent mannose complex and the Escherichia coli strain ORN178 that possesses mannose-specific receptor sites illustrates the potential for these complexes as biosensors.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Reference of 10049-08-8. Let’s face it, organic chemistry can seem difficult to learn. Especially from a beginner’s point of view. Like 10049-08-8, Name is Ruthenium(III) chloride. In a document type is Article, introducing its new discovery.

The band edges of p-GaInP2 are observed to migrate toward negative potentials during current flow under illumination in solutions with pH ranging from 1 to 14.5. The migration is not caused by a change in the pH of the semiconductor microenvironment but is a result of accumulation of photogenerated electrons at the p-GaInP2/water interface due to poor interfacial kinetics. This less than optimal interfacial charge-transfer rate can be catalyzed by treating the surface with transition-metal ions (e.g., RuIII, RhIII, CoIII, OsIII) which results in a suppression of band edge migration. As compared to an unmodified p-GaInP2 surface, the metal-ion treatment does not induce any appreciable band edge shift in the dark but effectively suppresses the band edge migration under illumination. RuIII and RhIII are found to act as better hydrogen-evolution catalysts than electrodeposited Pt.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Application of 10049-08-8, Chemistry can be defined as the study of matter and the changes it undergoes. You’ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.10049-08-8, Name is Ruthenium(III) chloride, molecular formula is Cl3Ru. In a patent, introducing its new discovery.

A new series of panchromatic ruthenium(II) sensitizers derived from carboxylated terpyridyl complexes of tris-thiocyanato Ru(II) have been developed. Black dye containing different degrees of protonation {(C2H5)3NH}[Ru(H3tcterpy)(NCS) 3] 1, {(C4H9)4N}2[Ru(H2 tcterpy)(NCS)3] 2, {(C4H9)4N}3[Ru(Htcterpy)(NCS) 3] 3, and {(C4H9)4N}4[Ru(tcterpy)(NCS) 3] 4 (tcterpy = 4,4?,4?-tricarboxy-2,2?:6?,2?-terpyridine) have been synthesized and fully characterized by UV-vis, emission. IR, Raman, NMR, cyclic voltammetry, and X-ray diffraction studies. The crystal structure of complex 2 confirms the presence of a RuIIN6 central core derived from the terpyridine ligand and three N-bonded thiocyanates. Intermolecular H-bonding between carboxylates on neighboring terpyridines gives rise to 2-D H-bonded arrays. The absorption and emission maxima of the black dye show a bathochromic shift with decreasing pH and exhibit pH-dependent excited-state lifetimes. The red-shift of the emission maxima is due to better pi-acceptor properties of the acid form that lowers the energy of the CT excited state. The low-energy metal-to-ligand charge-transfer absorption band showed marked solvatochromism due to the presence of thiocyanate ligands. The Ru(II)/(III) oxidation potential of the black dye and the ligand-based reduction potential shifted cathodically with decreasing number of protons and showed more reversible character. The adsorption of complex 3 from methoxyacetonitrile solution onto transparent TiO2 films was interpreted by a Langmuir isotherm yielding an adsorption equilibrium constant, Kads, of (1.0 ± 0.3) × 105 M-1. The amount of dye adsorbed at monolayer saturation was (na = 6.9 ± 0.3) × 10-8 mol/mg of TiO2, which is around 30% less than that of the cis-di(thiocyanato)bis(2,2?-bipyridyl-4,4?-dicarboxylate) ruthenium(II) complex. The black dye, when anchored to nanocrystalline TiO2 films achieves very efficient sensitization over the whole visible range extending into the near-IR region up to 920 nm, yielding over 80% incident photon-to-current efficiencies (IPCE). Solar cells containing the black dye were subjected to analysis by a photovoltaic calibration laboratory (NREL, U.S.A.) to determine their solar-to-electric conversion efficiency under standard AM 1.5 sunlight. A short circuit photocurrent density obtained was 20.5 mA/cm2, and the open circuit voltage was 0.72 V corresponding to an overall conversion efficiency of 10.4%.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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The nitrosation of [Ru(NH3)6]2+ in hydrochloric acid and alkaline ammonia media has been studied; the patterns of interconversion of ruthenium complexes in reaction solutions have been proposed. In both cases, nitrogen(II) oxide acts as the nitrosation agent. The procedure for the synthesis of [Ru(NO)(NH3)5]Cl3 ? H2O (yield 75-80%), the main nitrosation product of [Ru(NH 3)6]2+, has been optimized. Thermolysis of [Ru(NO)(NH3)5]Cl3 ? H2O in a helium atmosphere has been studied; the intermediates have been identified. One of these products is polyamidodichloronitrosoruthenium(II) whose subsequent decomposition gives an equimolar mixture of ruthenium metal and dioxide. The structure of trans-[RuNO(NH3)4Cl]Cl2, formed in the second stage of thermolysis and as a by-product in the nitrosation of [Ru(NH3)6]Cl2, has been determined by X-ray diffraction. Nauka/Interperiodica 2007.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 10049-08-8, Cl3Ru. A document type is Article, introducing its new discovery., Application In Synthesis of Ruthenium(III) chloride

Platinum group metal complexes of the general compositions M(Ligand)Cl3 [M = Ru(III), Ir(III)] and M(Ligand)Cl2 [M = Pd(II), Pt(II) have been synthesized [Ligand = 2,3,8,9-tetraphenyl-1,4,7,10-tetraazacyclododeca-1,3,7,9-tetraene(L 1), dibenzo[e,k]-2,3,-tetraphenyl-1,4,710-tetraazacyclododeca-1,3,7,9- tetraene (L2) and dibenzo[e,k]-2,3,8,9-tetramethyl-1,4,7,10-tetraazacyclododeca-1,3,7,9-tetraene (L3)]. The complexes have been characterized on the basis of elemental analyses, molar conductance, magnetic susceptibility measurements and electronic spectral studies. Sharp bands were observed in the electronic spectra of the complexes. The 8 values could not be reported as the spectra and been recorded in Nujol mulls. The Ru(III) and Ir(III) complexes have been found to stabilize an octahedral geometry while a square-planar geometry is assigned to the Pd(II) and Pt(II) complexes.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: Ruthenium(III) chloride. In my other articles, you can also check out more blogs about 10049-08-8

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Systematic fabrication of nanoparticle stabilizers can substantially modify the properties of prepared nanoparticles; here the synthesis of solubility adjustable nanoparticles is achieved by employing a family of polarity modulated stabilizers. The Royal Society of Chemistry 2009.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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A method for alkylation of at least one or more amino groups or mono-substituted amino groups, each on a carbon atom of a triazine ring of 1,3,5-triazine derivatives (melamine, melamine derivatives and various kinds of guanamine derivatives and the like), which includes reacting the 1,3,5-triazine derivatives having at least one or more amino groups or mono-substituted amino groups with alcohols in the presence of a catalyst of a metal of group VII and/or group VIII in the periodic table. The object of the invention is to provide a method for alkylation of 1,3,5-triazine derivatives, which includes alkylating amino groups or mono-substituted amino groups in carbon atoms of a 1,3,5-triazine ring, whereby substituted 1,3,5-triazine derivatives which are a group of useful compounds and which are widely used as intermediates of fine chemicals such as agricultural chemicals, medications, dye-stuffs, paints and the like, as resin materials and as flame-retardant materials can be easily produced in high yields.

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Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI

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The structure of oxide layers of the RuO2-IrO2/Ti electrode system and the thermal decomposition processes of RuCl3 and IrCl3 to form their respective oxides have been mainly analyzed by EXAFS (extended X-ray absorption fine structure) and XRD (X-ray diffraction). Upon heating of the respective chlorides in air, both chlorides convert into their respective oxides. The coordination numbers of the oxide ions around both the ruthenium and iridium ions increased with an increase in the calcination temperature and attained 6, which is the theoretical value of the standard samples of rutile RuO2 and IrO2. The changes in the coordination number with respect to the calcination temperature were accompanied by changes in the lattice constants of these oxides. This suggests that the deviation of these parameters from the standard sample is caused by the lattice defects of the oxide ions. A dependence of the radial distribution functions of EXAFS on the composition of the RuO2-IrO2/Ti electrode system showed that RuO2 forms a solid solution with IrO2 for the binary oxide electrode system.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI