Sep-21 News Awesome Chemistry Experiments For Dichloro(benzene)ruthenium(II) dimer

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The cyclometalation of chiral secondary amines through ortho-metalation of an aryl group occurred readily with [(eta6-benzene)RuCl 2]2 in acetonitrile. Reasonable to good yields of the expected cationic products of the form [(eta6-benzene)Ru(N-C)(NCMe) ](PF6), in which N-C represents the cyclometalated ligands, were obtained with bis-(R)-phenylethylamine, bis-(R)-1-naphthylethylamine, and (2R,5R)-2,5-diphenylpyrrolidine. Variable proportions of the expected four diastereoisomers were found according to NMR studies. The stereochemistry of complexes was investigated by 2D NMR in solution and by X-ray diffraction of single crystals. The (S) configuration at the metal was generally associated with a delta conformation of the metallacycle, and conversely, the (R) configuration with the lambda conformation.

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

9/23/21 News Final Thoughts on Chemistry for (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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Various macrocycles were prepared in one step by a novel ring-expansion method using olefin metathesis. Copyright

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

9/23/21 News Some scientific research about Ruthenium(III) chloride

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Several ruthenium(II) complexes with new tridentate polypyridine ligands have been prepared, and their photophysical properties have been studied. The new tridentate ligands are tpy-modified systems (tpy = 2,2?:6?,2?-terpyridine) in which aromatic substituents designed to be coplanar with the tpy moiety are introduced, with the aim of enhancing delocalization in the acceptor ligand of the potentially luminescent metal-to-ligand charge-transfer (MLCT) state and increasing the MLCT-MC energy gap (MC = metal-centered excited state). Indeed, the Ru(II) complexes obtained with this new family of tridentate ligands exhibit long-lived luminescence at room temperature (up to 200 ns). The enhanced luminescence properties of these complexes support this design strategy and are superior to those of the model Ru(tpy)22+ compound and compare favorably with those of the best Ru(II) complexes with tridentate ligands reported so far. Copyright

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

23-Sep News Final Thoughts on Chemistry for (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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The ring closing enyne metathesis of substrates with propargylic hindrance was investigated, revealing the successful combination of the Stewart-Grubbs catalysts and microwave heating sometimes up to 170 C for oxacycles. Medium-sized rings were obtained from terminal alkynes previously reputed as reluctant substrates. This unmatched combination was applied to the synthesis of carbocycles and oxacycles. In addition, this is the first report on the use of the Stewart Grubbs catalyst in ring closing enyne metatheses. (Figure Presented).

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

Sep-21 News Can You Really Do Chemisty Experiments About Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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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, Product Details of 15746-57-3

Three tripodal ligands 2,2?,2?-tris[(4,5-diazafluoren-9-ylimino)phenoxyethyl]amine (L1), 1,3,5-tris[(4,5-diazafluoren-9-ylimino)phenoxymethyl]-2,4,6-trimethylbenzene (L2), 1,1?,1?-tris[(4,5-diazafluoren-9-ylimino)phenoxymethyl]-1??-(p-tosyloxymethyl)-methane (L3), and corresponding Ru(II) complexes [(bpy)6L1-3(RuII)3](PF6)6 (Ru-L1-3) have been prepared. Cyclic voltammetry of the three complexes are consistent with one Ru(II)-centered quasi-reversible oxidation and three ligand-centered reductions. Photophysical behaviors are investigated by UV-Vis absorption and fluorescence spectrometry. The three complexes display metal-to-ligand charge transfer absorption at 445 nm and emission at 578 nm.

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

Sep-21 News Extended knowledge of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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A stereoselective total synthesis of leiocarpin C (2) and (+)-Goniodiol (1) by applying olefin cross-metathesis and substrate directed dihydroxylation as the key steps is reported (Schemea 3).

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

9/22/21 News Awesome Chemistry Experiments For Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)

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The catalytic activity of a series of ruthenium complexes for C-H amination reactions of organic azides was investigated. The most active catalyst was found to be RuCl3, which promotes C-H amination reactions of ortho-aryl phenylazides, l-azido-2-arylvinylazides, and 1-azido-1,3-butadienes to give carbazoles, indoles, and pyrroles, respectively. Both computational and experimental results support that a two-step process involving formal electrocyclization is involved in the catalytic reaction.

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

Sep-21 News Archives for Chemistry Experiments of Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C46H45ClP2Ru. In my other articles, you can also check out more blogs about 92361-49-4

92361-49-4, Name is Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II), molecular formula is C46H45ClP2Ru, belongs to ruthenium-catalysts compound, is a common compound. In a patnet, once mentioned the new application about 92361-49-4, Formula: C46H45ClP2Ru

2-Vinylic cyclic 1,3-alkadienes can be obtained with moderate to good yields via the Cp*RuCl(PPh3)2-catalyzed coupling reaction of alkynes with cyclic allenes. 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

Sep-21 News Awesome Chemistry Experiments For Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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A series of Ru(II) 2,2?-bipyridine (bpy) complexes with an electron-accepting dipyrido[3,2-A:2?,3?-c]phenazine (dppz) ligand coupled to an electron-donating triarylamine (TAA) group have been investigated. Systematic alteration of a bridging unit between the dppz and TAA allowed exploration into how communication between the donor and acceptor is perturbed by distance, as well as by steric and electronic effects. The effect of the bridging group on the electronic properties of the systems was characterized using a variety of spectroscopic methods, including Fourier transform-Raman (FT-Raman) spectroscopy, resonance Raman spectroscopy, and transient resonance Raman (TR2) spectroscopy. These methods were used in conjunction with ground- and excited-state absorption spectroscopy, electrochemical studies, and DFT calculations. The ground-state electronic absorption spectra show distinct variation with the bridging group, with the wavelength observed for the lowest energy electronic transition ranging from 449 nm to 522 nm, accompanied by large changes in the molar absorptivity. The lowest-energy Franck-Condon state was determined to be intra-ligand charge transfer (ILCT) in nature for most compounds. The presence of higher-energy metal-to-ligand charge transfer (MLCT) Ru(II) ? bpy and Ru(II) ? dppz transitions was also confirmed via resonance Raman spectroscopy. The TR2 spectra showed characteristic dppz?«- and TAA? »+ vibrations, indicating that the THEXI state formed was also ILCT in nature. Excited-state lifetime measurements reveal that the rate of decay is in accordance with the energy gap law and is not otherwise affected by the nature of the bridging unit.

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

9/22/21 News Archives for Chemistry Experiments of Dichloro(benzene)ruthenium(II) dimer

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The reactions of [RuCl(mu-Cl)(eta6-p-cymene)]2 with sodium carboxylates, in methanol or acetonitrile solution, afforded the complexes [RuCl(kappa2O-RCO2)(eta6-p-cymene)] (RCO2 = valproate, 1; aspirinate, 2; diclofenate, 3), in 79?96% yields. Analogously, [RuCl(kappa2O-dfCO2)(eta6-benzene)], 4, was obtained in admixture with minor by-products from [RuCl(mu-Cl)(eta6-benzene)]2 and sodium/silver diclofenate. The sequential reaction of [RuCl(mu-Cl)(eta6-p-cymene)]2 with sodium salicylate and PPh3 gave [Ru(kappa2O,O?-salCO2)(PPh3)(eta6-p-cymene)], 5, in 70% yield. The hydride complex [Ru2Cl2(mu-Cl)(mu-H)(eta6-p-cymene)2], 6, was produced in 36% yield from [RuCl(mu-Cl)(eta6-p-cymene)]2 and sodium formate. An optimization of the experimental work-up allowed to isolate [RuCl(mu-Cl)(eta6-p-cymene)]2 with an improved yield respect to the literature (98% vs. 65%). The bidentate coordination mode of the carboxylato ligands in 1?5 was unambiguously ascertained by IR and NMR spectroscopy, moreover the solid state structure of 1 was elucidated by single crystal X-ray diffraction. Complexes 1?3 experience rapid and quantitative dissociation of the carboxylato anion in DMSO/water/NaCl mixtures, mainly converting into [RuCl2(DMSO)(eta6-p-cymene)], 7.

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