Discovery of (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride

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The investigations disclosed offer insight regarding several key features of Ru-based catecholthiolate olefin metathesis catalysts. Factors influencing the facility with which the two anionic ligands undergo exchange and those that affect the rates of catalyst release are elucidated by examination of more than a dozen new complexes. These studies shed light on how different chelating groups can influence Ru-S bond strength and, as a result, the facility of catecholthiolate rotation. The trans influence series ether < ester ? iodide < amine ? thioether ? olefin < isonitrile ? phosphite has been established through X-ray structural analysis and shown to correlate well with the barrier for catecholthiolate rotation (trans effect) determined by variable-temperature NMR experiments and computational studies (DFT). It is found that, apart from electronic factors, chelate geometry has a more notable effect on the rate of catalyst release (five- vs six-membered chelate ring and mono- vs bidentate ligand). Polytopal processes involving pentacoordinate Ru(II) carbene complexes are shown to be distinct from previously reported fluxional events that involve tetracoordinate species and which are capable of causing diminished polymer syndiotacticity. Ru mercaptophenolate complexes have been synthesized and isolated as a single diastereomer (O-C trans to the NHC). This latter set of species promotes representative olefin metathesis reactions readily and gives Z selectivity levels that are higher than those when the corresponding catecholate systems are used, but less so in comparison to catecholthiolate complexes. A rationale for variations in stereoselectivity is presented. 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 301224-40-8 is helpful to your research., Application of 301224-40-8

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

Simple exploration of (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride

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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.301224-40-8, Name is (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride, molecular formula is C31H38Cl2N2ORu. In a Patent,once mentioned of 301224-40-8, Recommanded Product: 301224-40-8

This invention relates generally to olefin metathesis catalysts, to the preparation of such compounds, compositions comprising such compounds, methods of using such compounds, and the use of such compounds in the metathesis of olefins and in the synthesis of related olefin metathesis catalysts. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and in industrial applications such as oil and gas, fine chemicals, and pharmaceuticals.

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

Simple exploration of Dichloro(benzene)ruthenium(II) dimer

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Synthetic Route of 37366-09-9, 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.37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer, molecular formula is C12H12Cl4Ru2. In a patent, introducing its new discovery.

A process for the preparation of an enantiomerically enriched chiral amine of formula (10), or the opposite enantiomer thereof, from an imine of formula (11) wherein (i) R1 is aryl, R2 is alkyl and R3 is aryl or aryl-CH2-, or (iii) R2 is linked with R1 and/or R3 to form one or more rings and R3 or R1 (if not in a ring) is H or a non-interfering organic group, the number of C atoms in each of R1, R2 and R3 being up to 30, comprises asymetric hydrogenation of the imine in the presence of a base and, as catalyst, a ruthenium complex of a chiral diphosphine and a chiral diamine.

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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 (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

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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.246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, molecular formula is C46H65Cl2N2PRu. In a Article,once mentioned of 246047-72-3, Product Details of 246047-72-3

Pantothenamides are known for their in vitro antimicrobial activity. Our group has previously reported a new stereoselective route to access derivatives modified at the geminal dimethyl moiety. This route however fails in the addition of large substituents. Here we report a new synthetic route that exploits the known allyl derivative, allowing for the installation of larger groups via cross-metathesis. The method was applied in the synthesis of a new pantothenamide with improved stability in human blood.

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

Extracurricular laboratory:new discovery of Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)

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Application of 32993-05-8, 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.32993-05-8, Name is Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II), molecular formula is C41H35ClP2Ru. In a patent, introducing its new discovery.

Reactions between 1,1?-(Me3SiC{triple bond, long}C)2Rc? [Rc? = ruthenocen-1,1?-diyl, Ru(eta-C5H4-)2] and RuCl(PP)Cp? in the presence of KF gave 1,1?-{Cp(PP)RuC{triple bond, long}C}2Rc? [Cp? = Cp, PP = PPh3 1, P(m-tol)3 2, dppe 3, dppf 4; Cp? = Cp*, PP = dppe 5]. Compounds 1 and 2 react with tcne to give two diastereomers a/b of the allylic (vinylcarbene) complexes 6 and 7, while methylation of 5 gave the bis-vinylidene [1,1?-{Cp*(dppe)Ru{double bond, long}C{double bond, long}CMe}2Rc?](BPh4)2 (8). The X-ray structures of 4, 6b and 8 have been determined. Cyclic voltammograms indicate that there is some electronic communication between the ruthenium end-groups through the Rc? centre.

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

Discovery of (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride

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Application of 301224-40-8, 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.301224-40-8, Name is (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride, molecular formula is C31H38Cl2N2ORu. In a patent, introducing its new discovery.

Stereospecific [3,3]-sigmatropic rearrangement of O-substituted thiocarbamate derivatives of enantiopure allylic alcohols provides allylic thiocarbamates as single enantiomers. Intramolecular arylation by rearrangement of their allyllithium derivatives provides allylic tertiary thiols. Allylation and ring-closing metathesis gives 2,5-dihydrothiophenes containing sulfur-bearing quaternary centres. This journal is the Partner Organisations 2014.

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

Archives for Chemistry Experiments of 37366-09-9

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Polypyridyl ruthenium complexes have been intensively investigated for their remarkable antiproliferative properties and some are currently being tested in clinical trials. Here, we investigated the impact of illumination on the biological properties of a series of new cyclometalated ruthenium compounds with increased pi-conjugation. We determined that various of these complexes display a bivalent biological activity as they are highly cytotoxic by themselves in absence of light while their cytotoxicity can significantly be elevated towards an IC50 in the nanomolar range upon illumination. In particular, we showed that these complexes are particularly active (IC50 < 1 muM) on two gastric cancer cell lines (AGS, KATO III) that are resistant towards cisplatin (IC50 > 25 muM). As expected, light activation leads to increased production of singlet oxygen species in vitro and accumulation of reactive oxygen species in vivo. Importantly, we established that light exposure shifts the mode of action of the complexes towards activation of a caspase 3-dependent apoptosis that correlates with increased DNA damage. Altogether, this study characterizes novel ruthenium complexes with dual activity that can be tuned towards different mode of action in order to bypass cancer cell resistance mechanisms.

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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 Dichloro(benzene)ruthenium(II) dimer

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In an article, published in an article, once mentioned the application of 37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer,molecular formula is C12H12Cl4Ru2, is a conventional compound. this article was the specific content is as follows.category: ruthenium-catalysts

Selective reduction of 2-nitro-3-methoxybenzaldehyde provides 2-amino-3-methoxybenzaldehyde that undergoes the Friedlaender condensation with a variety of acetyl-substituted derivatives of pyridine and 1,10-phenanthroline. After cleavage of the methyl ether, the resulting polydentate analogues of 8-hydroxyquinoline are excellent ligands for ruthenium. The resulting oxidation state of the metal center depends on the anionic character of the ligands. The presence of two electron donating anionic ligands results in a Ru(III) complex as evidenced by paramagnetic NMR behavior. The electronic absorption and redox properties of the complexes were measured and found to be consistent with the anionic character of the 8-HQ moieties. A planar pentadentate ligand provides two Ru-O and two Ru-N bonds in the equatorial plane. An X-ray structure shows that the central pyridine of the ligand is oriented toward the metal but held at a distance of 2.44 A.

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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 Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II)

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The electrochemical behaviour of the ruthenium(II) alkyl complexes [Ru(Me)Cp*(L)2] (Cp=eta5-C5Me5; L=PMe3 2a, PMe2Ph 2b), [Ru(CH2CMe3)Cp*(PMe3)2] (3a), and the related [Ru(Me)Cp(PPh3)2] (4d) (Cp=eta5-C5H5) in CH2Cl2 involves a one-electron process, yielding the corresponding ruthenium(III) paramagnetic cations, as shown by coupled electrochemical-EPR studies. Compounds 2-4 are oxidised by [FeCp2]+ in benzene to unidentified paramagnetic products which may decompose giving the corresponding alkane. The Cp* compounds react with NOBF4 affording the monocationic alkylnitrosyl derivatives [Ru(R)Cp*(NO)(L)]BF4 (R=Me; L=PMe3 7a, PMe2Ph 7b. R=CH2CMe3; L=PMe3) and, when in excess of NO+, the ruthenium(II) dicationic complexes [RuCp*(NO)(L)2](BF4)2 (L=PMe3 5a, PMe2Ph 5b). The chloro complexes [Ru(Cl)Cp*(L)2] (L=PMe3 1a, PMe2Ph 1b, PPh3 1d) react analogously with NO+ to give [Ru(Cl)Cp*(NO)(L)]BF4 (L=PMe3 6a, PMe2Ph 6b, PPh3 6d) and [RuCp*(NO)(L)2](BF4)2 (L=PMe3 5a, PMe2Ph 5b). In contrast [Ru(Me)Cp(PPh3)2] gives only [Ru(Me)Cp(NO)(PPh3)]BF4. EPR spectroscopy suggests that these nitrosylation reactions are also oxidative in character proceeding through ruthenium(III) intermediates.

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

Awesome Chemistry Experiments For Chloro(pentamethylcyclopentadienyl)bis(triphenylphosphine)ruthenium(II)

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The indenyl and pentamethylcyclopentadienyl ruthenium(II) complexes [(eta5-L3)Ru(L2)Cl] (L3 = C 9H7, L2 = dppe (1a), L2 = dppm (1b) ; L3 = C5Me5, L2 = dppe (2a); L 2 = dppm (2b) (where, dppe = Ph2PCH2CH 2PPh2 and dppm = Ph2PCH2PPh 2) reacts with NaN3 to yield the azido complexes [(eta5-C9H7)Ru(L2)N3], L2 = dppe (3a), dppm (3b) and [(eta5-C 5Me5)Ru(L2)N3], L2 = dppe (4a), dppm (4b), respectively. The azido complexes undergo [3 + 2] dipolar cycloaddition reaction with dimethylacetylenedicarboxylate to yield triazole complexes [(eta5-C9H7)Ru(L 2)(N3C2(CO2Me)2)], L 2 = dppe (5a), dppm (5b) and [(eta5-C5Me 5)Ru(L2)(N3C2(CO2Me) 2)], L2 = dppe (6a), dppm (6b), respectively. The complexes were fully characterized on the basis of microanalyses, FT-IR and NMR spectroscopy. The crystal structures of the starting complex (1a) and representative complexes 5a, 5b and 6a have been established by single X-ray study.

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