Can You Really Do Chemisty Experiments About Dichloro(benzene)ruthenium(II) dimer

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37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer, molecular formula is C12H12Cl4Ru2, belongs to ruthenium-catalysts compound, is a common compound. In a patnet, once mentioned the new application about 37366-09-9, name: Dichloro(benzene)ruthenium(II) dimer

(Figure Presented) Alkane and arene join together: Various arenes were coupled directly with simple cycloalkanes. The reaction was catalyzed by ruthenium under oxidative conditions to give substituted cycloalkylarenes regioselectively (see scheme).

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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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In an article, published in an article, once mentioned the application of 15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II),molecular formula is C20H16Cl2N4Ru, is a conventional compound. this article was the specific content is as follows.SDS of cas: 15746-57-3

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

Discovery of Dichloro(benzene)ruthenium(II) dimer

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 37366-09-9 is helpful to your research., Application of 37366-09-9

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A ruthenium-dioxolene-amine complex, [RuIII(NH 2-L)(Bu2sq)](PF6)2·0.5H 2O (NH2-L = bis(2-pyridylmethyl)-2-aminoethylamine, Bu2sq- = 3,5-di-tert-butylsemiquinonate), was newly prepared. The complex undergoes spontaneous one-electron reduction under basic conditions in MeOH and works as an electrocatalyst in the oxidation of benzyl alcohol to benzaldehyde under electrolysis at +0.4 V (vs SCE).

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

Top Picks: new discover of 15746-57-3

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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., COA of Formula: C20H16Cl2N4Ru

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

Awesome and Easy Science Experiments about Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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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

Discovery of Dichloro(benzene)ruthenium(II) dimer

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New series of half-sandwich ruthenium(II) complexes supported by a group of bidentate pyridylpyrazole and pyridylimidazole ligands [(eta6-C6H6)Ru(L2)Cl][PF6] (1), [(eta6-C6H6)Ru(HL3)Cl][PF6] (2), [(eta6-C6H6)Ru(L4)Cl][PF6] (3), and [(eta6-C6H6)Ru(HL5)Cl][PF6] (4) [L2, 2-[3-(4-chlorophenyl)pyrazol-1-ylmethyl]pyridine; HL3, 3-(2-pyridyl)pyrazole; L4, 1-benzyl-[3-(2?-pyridyl)]pyrazole; HL5, 2-(1-imidazol-2-yl)pyridine] are reported. The molecular structures of 1-4 both in the solid state by X-ray crystallography and in solution using 1H NMR spectroscopy have been elucidated. Further, the crystal packing in the complexes is stabilized by C-H?X (X = Cl and pi), N-H?Cl, and pi-pi interactions.

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

The important role of Dichloro(benzene)ruthenium(II) dimer

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The invention discloses a ruthenium complex, with a light-activated antibacterial function, which has the structure I shown : Wherein, R is selected from H or – OCH. 3 ;X. A monovalent anion, representing a balanced charge, which has the ability, to penetrate cell membranes and bacteria, does not possess the ability, to penetrate the nucleus but has a strong lethality on the bacteria under light conditions, to overcome the resistance, of bacteria to traditional chemotherapeutic antibiotics, and the invention also discloses a preparation method and application, of the complex. (by machine translation)

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

Can You Really Do Chemisty Experiments About Dichloro(benzene)ruthenium(II) dimer

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C12H12Cl4Ru2, you can also check out more blogs about37366-09-9

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p53 is a key tumor suppressor gene involved in key cellular processes and implicated in cancer therapy. However, it is inactivated in more than 50% of all cancers due to mutation or overexpression of its negative regulators. This leads to drug resistance and poor chemotherapeutic outcome as most clinical drugs act via a p53-dependent mechanism of action. An attractive strategy to circumvent this resistance would be to identify new anticancer drugs that act via p53-independent mode of action. In the present study, we identified 9 Ru (II)-Arene Schiff-base (RAS) complexes able to induce p53-independent cytotoxicity and discuss structural features that are required for their p53-independent activity. Increasing hydrophobicity led to an increase in cellular accumulation in cells with a corresponding increase in efficacy. We further showed that all nine complexes demonstrated p53-independent activity. This was despite significant differences in their physicochemical properties, suggesting that the iminoquinoline ligand, a common structural feature for all the complexes, is required for the p53-independent activity.

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

Some scientific research about Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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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