The Absolute Best Science Experiment for Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru, belongs to ruthenium-catalysts compound, is a common compound. In a patnet, once mentioned the new application about 15746-57-3, Application In Synthesis of Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

Two ruthenium(II) complexes of newly designed pyrrol-azo ligands(L) and bipyridine(bpy) formulated as [Ru(L)(bpy)2]ClO4, where HL1= (4-chloro-phenyl)-(1H-pyrrol-2-yl)-diazene (1) complex 1 and HL2= (4-nitro-phenyl)-(1H-pyrrol-2-yl)-diazene for 2, were isolated in pure form. The complexes were characterized by physicochemical and spectroscopic methods. The electrochemical behavior of the complexes showed the Ru(III)/Ru(II) couple at different potentials with quasi-reversible voltammograms. The study of cytotoxicity effects of 1 and 2 on human breast cancer cells (,were isolated in pure form. The complexes were characterized by physicochemical and spectroscopic methods. The electrochemical behavior of the complexes showed the Ru(III)/Ru(II) couple at different potentials with quasi-reversible voltammograms. The study of cytotoxicity effects of 1 and 2 on human breast cancer cells (MCF 7, MDA-MB 231) and cervical cancer cell (HeLa) taking Cisplatin as a positive reference showed that 1 exhibited higher cytotoxicity against cancer cell lines than 2, but less activity than Cisplatin. The interaction of 1 with calf thymus DNA (CT-DNA) using absorption, emission spectral studies, viscosity-measurement, and electrochemical techniques has been used to determine the binding constant Kband the linear Stern-Volmer quenching constant KSV. The results indicate that 1 strongly interacts with CT-DNA in groove binding mode. The interaction of bovine serum albumin (BSA) with 1 was also investigated with the help of spectroscopic tools. Absorption spectroscopy proved the formation of a BSA-[Ru(L1)(bpy) 2]ClO4 complex.

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

A new application about Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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Ruthenium complexes containing pdon (pdon = 1,10-phenanthroline-5,6-dione) were synthesized. Their spectroscopic and electrochemical properties were examined. The molecular structure with [Ru(pdon)(bpy)2](ClO 4)2 ([1](ClO4)2) (bpy = 2,2?-bipyridyl) was determined by single crystal X-ray diffraction. The optically transparent thin-layer electrochemical measurements confirm that the quinone form of [1](ClO4)2 is reduced to the semi-quinone state in acetonitrile (E? = -8 mV). Comparing the model complex, [1](ClO4)2, and metal-free pdon, the positive charge on two carbon atoms of the o-quinone group is bigger than that of metal-free pdon. The assemblies of the complexes were finally examined using ligand substitution.

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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 new click-adduct 4,5-di(2-pyridyl)-1,2,3-triazole acts as a doubly-chelating anionic bridging ligand that forms dinuclear ruthenium(ii) complexes which exhibit strong metal-metal interactions. The Royal Society of Chemistry.

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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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Novel redox-active DNA labeling tags with tunable electrochemical potentials are modularly synthesized using (a) bis-substituted Ru2+ or Os2+ precursors (R2bpy)2ML2, (b) substituted 2,4-pentanediones or hydroxamic acids bearing a functionalized linker, and (c) modified nucleotides. DNA polymerase efficiently incorporates the metal-containing nucleotide triphosphate into DNA oligonucleotides. Copyright

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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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With the radical 2?,5?-dihydro-4?,5?,5?-trimethyl-spiro-[4,5- diazafluorene-9,2?-imidazol]-1-oxyl L a series of transition metal complexes has been prepared: [ML3](SbF6)2· 4H2O with M2+ = Mn2+ (1), Fe2+ (2), Co2+ (3), Ni2+ (4), Zn2+ (5). Reaction of L with Cu2+ in methanol yielded different products depending on the counterion. In the presence of weakly coordinating anions the Cu(I) complexes [Cu2L3](SbF6)2 · H2O (6), [Cu2L3](OTf)2 · 2MeOH (7) and [Cu2L3](ClO4)2 (8) were formed. Stronger coordinating counter ions gave the complexes CuL2Cl2 · H2O (9), CuL2Br2 · H2O (10) and CuL2(NO3)2 (11). Also the synthesis of [Ag2L3](SbF6)2 · 2H2O (12), Pd(L)Cl2 · H2O (13), Pt(L)Cl2 · H2O (14), Ni(L)Cl2 (15a), Ni(L)Cl2 · 4H2O (15b) and [Ru(bipy)2(L)]Cl2 · 4H2O (16) is reported. The magnetic moments of 1-6 and 10 correspond in the range 200-300 K to those expected for noninteracting spins of the metal ion and the radicals. At low temperatures spin pairing of metal and radical spins is observed for 1-3.

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

Discovery of Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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The attachment of two polyethylene glycol tails (n = 7, MW = 350) to ruthenium tris(bipyridine) via ester links on the 4,4′-positions of one of the bipyridine ligands yields a highly viscous (eta ? 107 cP) molten salt (abbreviated [Ru(bpy)2(bpy(CO2MePEG350)2)](ClO4)2) that glasses at ca. – 5 C. At room temperature, the ionic conductivity of the melt is sufficiently high that application of 2.4 V across the fingers of a Pt interdigitated electrode array (IDA) coated with the melt leads to the electrolytic development of serial concentration gradient microstructures of Ru(III/II) and Ru(II/I) states. At the intersection of the two concentration gradients, in the interior of the coating, reaction between the Ru(III) and Ru(I) states leads to ECL emission with an efficiency of 0.2% photons/electron. Cooling a concentration gradient-containing film to -20 C under voltage bias, so as to preserve the gradient microstructure, yields a film that has an emission efficiency of 0.1%, a current and light emission response that rapidly changes with the applied voltage bias, and a diode- like current-voltage profile with a ca. 100 rectification ratio.

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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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A water-soluble metallo-supramolecular polymer MSP-f-6Np, which possesses a regular pore aperture of 1.4 nm, has been assembled from a structurally flexible naphthalene-appended [Ru(bipy)3]2+ complex and cucurbit[8]uril. As the first periodic metallo-supramolecular polymer formed by a flexible building block, MSP-f-6Np exhibits a hydrodynamic diameter of 122 and 164 nm at 0.1 and 2.0 mM of the monomer concentrations. Synchrotron small angle X-ray scattering experiments confirm that MSP-f-6Np possesses porosity periodicity in both the solution and solid states. Compared with a control, the new highly ordered porous system displays enhanced photocatalytic activity for the degradation of organic dyes.

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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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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. 15746-57-3, C20H16Cl2N4Ru. A document type is Article, introducing its new discovery., HPLC of Formula: C20H16Cl2N4Ru

Covalently linked bipyridyl ligands (L-L) with alkyl linkages varying from (-CH2-)2 to (-CH2-)12 were used to prepare ruthenium oxo dimers of the form [(bpy) (H2O)RuO(L-L)Ru(2O) (bpy)]4+. The bridging alkyl linkage increases the stability of these oxo dimers by maintaining the relative proximity of the two ruthenium centers even when the oxo bridge is cleaved. These complexes have been characterized by electronic spectroscopy and electrochemistry. The electrochemistry in CH3CN/0.1M TBAP exhibits a reversible one-electron oxidation followed by a second reversible two-electron oxidation which becomes catalytic in aqueous solution. The catalytic generation of dioxygen from water was observed upon bulk electrolysis of the oxo dimer at +1.39 V.

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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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A one-pot synthesis of three new macrocycles containing two, three or four 2,2′-bipyridine units is described; the X-ray analysis of the bis-bipyridine ligand reveals a cyclophane type structure; the X-ray structure of one of the diastereoisomers of the dinuclear ruthenium complex is also described and shows two metal centres held in close proximity.

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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 disclosure provides methods of converting a lower alcohol (e.g., ethanol) to a higher alcohol (e.g., butanol) in the presence of a water stable transition metal catalyst comprising a Group VIII transition metal and a polydentate nitrogen donor ligand. The methods described in the disclosure can be carried out in the presence of water and achieve high purities of the higher alcohols.

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