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Synthesis and characterization of a new cyclophosphazene and its ruthenium complex derived from 1,10-phenanthroline-5,6-diol

A new spirocyclic phosphazene derivative has been synthesized from the reaction of 1,10-phenanthroline-5,6-diol with hexachlorocyclotriphosphazatriene in suitable conditions and the Ru(II) complex of the ligand was prepared and characterized. Synthesized compounds have been investigated with the methods of FTIR, 1H NMR, 31P NMR, UV-VIS, MS, fluorescence and elemental analysis.

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Reference£º
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.HPLC of Formula: C20H16Cl2N4Ru. In my other articles, you can also check out more blogs about 15746-57-3

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru. In a Article£¬once mentioned of 15746-57-3, HPLC of Formula: C20H16Cl2N4Ru

A mitochondria-targeting dinuclear Ir-Ru complex as a synergistic photoactivated chemotherapy and photodynamic therapy agent against cisplatin-resistant tumour cells

A mitochondria-targeting hetero-binuclear Ir(iii)-Ru(ii) complex was developed as a photoactivated chemotherapy (PACT) and photodynamic therapy (PDT) bifunctional agent to achieve a synergistic effective therapeutic outcome for the therapy of cisplatin-resistant tumour cells.

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Reference£º
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.37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer, molecular formula is C12H12Cl4Ru2. In a Article£¬once mentioned of 37366-09-9, Recommanded Product: Dichloro(benzene)ruthenium(II) dimer

Design of Ru(II)-NHC-Diamine Precatalysts Directed by Ligand Cooperation: Applications and Mechanistic Investigations for Asymmetric Hydrogenation

A modular synthesis of Ru(II)-NHC-diamine complexes from readily available chiral N-heterocyclic carbenes (NHCs) and chiral diamines is disclosed for the first time. The well-defined Ru(II)-NHC-diamine complexes show unique structure and coordination chemistry including an unusual tridentate coordination effect of 1,2-diphenylethylenediamine. The isolated air- A nd moisture-stable Ru(II)-NHC-diamine complexes act as versatile precatalysts for the asymmetric hydrogenation of isocoumarines, benzothiophene 1,1-dioxides, and ketones. Moreover, on the basis of the identification of reaction intermediates by stoichiometric reactions and NMR experiments, together with the DFT calculations, a possible catalytic cycle was proposed.

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Reference£º
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.15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru. In a Article£¬once mentioned of 15746-57-3, Quality Control of: Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

Ancillary ligand determination of the spin location in both oxidised and reduced forms of diruthenium complexes bridged by bis-bidentate 1,4-bis(2-phenolato)-1,4-diazabutadiene

The rare bridging mode of 1,4-bis(2-phenolato)-1,4-diazabutadiene = glyoxalbis(2-hydroxyanil) (L2-) is adopted in {(-L 2-)[RuII(bpy)2]2}2+ (12+), obtained as bis-perchlorate. Four well accessible redox forms of 1n (n = 4+, 3+, 2+, +) have been characterised by UV-VIS-NIR spectroelectrochemistry. The (3+) and (+) intermediates have also been investigated by EPR, both showing radical-type signals close to g = 2. This observation stands in stark contrast to EPR results previously obtained for the related {(-L)[Ru(acac)2]2}n, n = + and -, both of which exhibit metal-centred spin. In combination with the UV-VIS-NIR spectra these results suggest the preferential involvement of the multistep ligand redox system Ln- in the electron transfer processes. The relative stabilisation of RuII by pi-accepting bpy is made responsible for the oxidation of the ligand L2- instead of the metal. The Royal Society of Chemistry 2007.

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

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A Tris(bipyridine)ruthenium(II)-beta-cyclodextrin derivative: Synthesis, luminescent properties, and application in electrochemiluminescence DNA sensors

Miraculous metallocyclodextrin: A new polynuclear metallocyclodextrin complex, tris(bpyRu)-beta-CD (bpy=bipyridine), was successfully synthesized. This complex possesses molecular-recognition functions and unique luminescent properties. A tris(bpyRu)-beta-CD film was fabricated and utilized in a electrochemiluminescence (ECL) DNA sensor based on its molecular-recognition and luminescence characteristics (see scheme). Copyright

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

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Reference of 37366-09-9. Let¡¯s face it, organic chemistry can seem difficult to learn. Especially from a beginner¡¯s point of view. Like 37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer. In a document type is Article, introducing its new discovery.

Metalloradical Reactivity of RuI and Ru0 Stabilized by an Indole-Based Tripodal Tetraphosphine Ligand

The tripodal, tetradentate tris(1-(diphenylphosphanyl)-3-methyl-1H-indol-2-yl)phosphane PP3-ligand 1 stabilizes Ru in the RuII, RuI, and Ru0 oxidation states. The octahedral [(PP3)RuII(Cl)2] (2), distorted trigonal bipyramidal [(PP3)RuI(Cl)] (3), and trigonal bipyramidal [(PP3)Ru0(N2)] (4) complexes were isolated and characterized by single-crystal X-ray diffraction, NMR, EPR, IR, and ESI-MS. Both open-shell metalloradical RuI complex 3 and the closed-shell Ru0 complex 4 undergo facile (net) abstraction of a Cl atom from dichloromethane, resulting in formation of the corresponding RuII and RuI complexes 2 and 3, respectively.

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

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Synthesis of 2-hydroxymethyl-5-amine methyl furan the method of the compound (by machine translation)

Synthesis of 2-hydroxymethyl-5-amine methyl furan the method of the compound belongs to the field of chemical synthesis. The method in accordance with the following steps: to measure complex two price rutheniums, amine substrate, 5-hydroxy methyl furfural is dissolved in a solvent, in order to 5-hydroxymethyl-furfural as the raw material, hydrogen as reducing agent, two price rutheniums complex as a catalyst, for the reductive amination, wherein amine substrate, two price rutheniums complex, 5-hydroxy methyl furfural amount-of-substance ratio of 1.0-2.0: 0.001-0.01: 1 ; the hydrogen pressure is 1.0-2.0 MPa; the reaction temperature is 30-100 C; the reaction time is:4-36h; synthesis of 2-hydroxymethyl-5-amine methyl furfuran compound. The beneficial results of this invention are: ruthenium complex as the catalyst, hydrogen as reducing agent, the operation is simple, low cost of raw materials, the reaction efficiency is high. (by machine translation)

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

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Monocationic mu-diborolyl triple-decker complexes [CpCo(mu-1,3-C 3B2Me5)M(ring)]+: Synthesis, structures, and electrochemistry

Cationic triple-decker complexes with a bridging diborolyl ligand, [CpCo(mu-1,3-C3B2Me5)M(ring)]+ (M(ring) = CoCp (2a), CoCp* (2b), RhCp (3a), RhCp* (3b), IrCp (4a), IrCp* (4b), Ru(C6H6) (5a), Ru(p-MeC 6H4Pri) (5b), Ru(C6Me6) (5c), Ru(eta6-cycloheptatriene) (6)), were synthesized by reaction of CpCo(mu-1,3-C3B2Me5)Tl with [M(ring)Hal2]2. The structures of 2aBPh4, 2bPF6, 4aPF6, 5aOTf, and 5cPF6 were determined by X-ray diffraction. The electron-transfer ability of the complexes has been ascertained by electrochemical and spectroelectrochemical techniques. In general, they are able to shuttle reversibly in the sequence 2+/+/0/-, plausibly affording completely delocalized mixed-valence derivatives. DFT calculations revealed structural changes accompanying redox processes and satisfactorily predicted the potentials for the first reduction and first oxidation.

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Reference£º
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.15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru. In a Article£¬once mentioned of 15746-57-3, Application In Synthesis of Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

[Ru(bpy)2(dppz-NH2)]2+ complex (dppz-NH2: 7-Amino-dipyrido [3,2-a : 2′,3′-c]phenazine) as a useful photosensitizing unit for the construction of photoinduced energy transfer systems

7-Amino-dipyrido[3,2-a:2′,3′-c]phenazine (dppz-NH2) has a diimine coordination site, a rigid and extended pi conjugation system, and a reactive amino group within the molecule, and [Ru(bpy)2(dppz-NH2)]2+ was synthesized as a useful photosensitizing unit for the construction of photoinduced energy-transfer systems. Anthraquinone, anthracene, and [Os(bpy)3]2+ derivatives having a carboxylic acid function were used as energy-accepting units, and were successfully connected to [Ru(bpy)2(dppz-NH2)]2+ through an amide bond. Electronic spectral and electrochemical studies of the resultant complexes were carried out, and it was shown that effective excited electron or energy transfer took place from the Ru(II) polypyridyl center to these units. In the case of the heterodinuclear Ru(II)/Os(II) complex, emission from the Ru(II) polypyridyl center was effectively quenched and that from the Os(II) polypyridyl center was increased compared to the reference Os(II) polyimine complex. The rate of energy transfer from the Ru(II) to the Os(II) polypyridyl, center through the dppz-amide connector was estimated to be 1.0 x 108 s-1 in acetonitrile.

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

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Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.COA of Formula: C20H16Cl2N4Ru, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 15746-57-3, in my other articles.

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 15746-57-3, Name is Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II), molecular formula is C20H16Cl2N4Ru. In a Article£¬once mentioned of 15746-57-3, COA of Formula: C20H16Cl2N4Ru

Ruthenium(II) bipyridyl complexes as photolabile caging groups for amines

The synthesis and characterization of a series of ruthenium bis(bipyridine) complexes where the inorganic moiety acts as a photolabile protecting group is described. Complexes of the type [Ru(bpy)2L2]+ where bpy = 2,2?-bipyridine and L = butylamine, gamma-aminobutyric acid, tyramine, tryptamine, and serotonin were studied by nuclear magnetic resonance, cyclic voltammetry, and electronic absorption spectroscopy. In all cases, ligands are coordinated by the amine group. The complexes are stable in water for several days and deliver one molecule of ligand upon irradiation with visible light (450 nm). These properties make them suitable for their use as biological caged compounds.

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