Ruthenium catalysts

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, Recommanded Product: Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

The functionalized ruthenium(II)polypyridine complexes for the highly selective sensing of mercury ions

A series of new ruthenium(II)polypyridine complexes appending with thioether groups were designed, synthesized and characterized. The sensing ability of the complexes toward mercury ions were studied by electronic absorption and emission spectra, and the reaction of the complexes with mercury ions were also confirmed by ESI mass spectroscopy and 1HNMR spectroscopy. The thioether groups would react with mercury ion fast to form aldehyde group leading to the significant change in the spectra. The color of the complex changed from yellow to orange after addition of mercury ions, and the color of the emission changed from red orange to dark red with a large red shift (~80 nm). Importantly, these kinds of ruthenium(II)complexes show a unique recognition of mercury ions over other metal ions. The complexes with more thioether groups also showed a better sensitivity toward mercury ions, this is good strategy for the further design of the new phosphorescent probes for sensing of mercury ions.

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

Reference of 37366-09-9. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 37366-09-9, Name is Dichloro(benzene)ruthenium(II) dimer

Organo-ruthenium supported heteropolytungstates: synthesis, structure, electrochemistry, and oxidation catalysis

The reaction of [Ru(arene)Cl2]2 (arene = benzene, p-cymene) with [X2W22O74(OH)2] 12- (X = SbIII, BiIII) In buffer medium resulted In four organo-ruthenium supported heteropolytungstates, [Sb 2W20O70(RuC6H6) 2]10 (1), [Bi2W20O 70(RuC6H6)2]10- (2), [Sb2W20O7o(RuC10H14) 2]10- (3), and [Bi2W20O 70(RuC10H14)2]10- (4), which have been characterized in solution by multinuclear (183W, 13C, 1H) NMR, UV-vis spectroscopy, electrochemistry, and in the solid state by single-crystal X-ray diffraction, IR spectroscopy, thermogravimetric analysis, and elemental analysis. Polyanions 1, 2, and 4 crystallize in the triclinic system, space group P1 with the following unit cell parameters: K5Na5[Sb2W20O 7o(RuC6H6)2]¡¤22H 2O (KNa-1), a= 12.1625(2)A, b = 13.1677(2) A, C= 16.0141(3)A alpha = 78.9201 (7), beta = 74.4442(8), gamma = 78.9019(8), and Z= 1 ; Cs2Na8[Bi2W 20O7o(RuC6H6)2] ¡¤ 30H2O (CsNa-2), a = 11.6353(7) A b = 13.3638(7) A, C= 16.7067(8) A, a = 79.568(2), beta = 71.103(2), gamma = 80.331(2), and Z= 1; Na10[Bi2W20O 70(RuC10H14)2]-35H20 (Na-4), a = 15.7376(12) A b = 15.9806(13) A, c = 24.2909(19) A, alpha = 92.109(4), beta = 101.354(4), gamma = 97.365(3), and Z= 2. Polyanions 1-4 consist of two (L)Ru2+ (L = benzene or p-cymene) units linked to a [X2W20O70]14 (X=Sb III BiIII fragment via Ru-O(W) bonds resulting in an assembly with idealized C2h symmetry. Polyanions 1-4 are stable in solution as indicated by the expected 183W, 13C, and 1H NMR spectra. The electrochemistry of 1-4 is described by considering the reduction and the oxidation processes. The nature of the arene In Ru(arene) has practically no influence on the formal potentials of the W-centers, which are more sensitive to the Sb or Bi hetera atoms. The results suggest that the respective Sb- and Bi derivatives have very different pK a values, with the reduced form of 1 being the most basic, thus permitting the observation of two well-developed voltammetric waves at pH 6. In contrast, the identity of the arene influences the oxidation processes, thus permitting to distinguish them. A strong electrocatalytic water oxidation peak is observed that is more positive than the one corresponding to the Ru(arene) oxidation process. Also a stepwise oxidation of the Ru(benzene) group could be observed at pH 3. The catalytic efficiency, on the other hand, of 1-4 toward the oxidation of n-hexadecane and p-xylene illustrated the effect of ruthenium substitution on the polyanion catalytic performance.

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

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.Recommanded Product: Dichloro(benzene)ruthenium(II) dimer

Structural elucidation and antibacterial studies on half-sandwich ruthenium(II) complexes incorporating arene, phosphine, arsine and thioamide ligands

The half-sandwich arene complexes of ruthenium(II) incorporating arsine, phosphine and thioamide ligands with formula [Ru(eta6-arene)(ER3)(AEtT)]+BPh4-eta6-arene = C6H6 or p-cymene; E = P/As; R = C6H5/C6H5CH2; AEtT = 4-amino-3-ethyl-5-mercapto-1,2,4-triazole bidentate mononegative anion) are prepared and investigated. The reaction products have been characterized by elemental analyses, conductometric, magnetic, IR, UV-visible and 1H NMR spectra. Antibacterial activities of ligand and complexes are tested against E. coli, B. subtilus and S. aureus. The data revealed that all the complexes are more active than free thioamide ligand.

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

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium, Safety of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium.

Synthesis and reactivity of oxygen chelated ruthenium carbene metathesis catalysts

The rate of initiation of Hoveyda catalysts is affected by the electronic and steric effects that act upon the Rua?O coordination. In order to boost the activity of Hoveyda catalysts, a series of new oxygen chelated ruthenium carbene metathesis catalysts containing an N-heterocyclic carbene (NHC) and a carbonyl group has been developed, and their catalytic activities for olefin metathesis reactions were investigated. The aliphatic end groups of complexes (H2IMes)(Cl)2RuC(H)[(C6H 3X)OCH(Me)(C(O)OEt)(X = H, OMe, Me, NO2)] were functionalized by the attachment of a straight-chain ester. The X-ray structures of complex (H2IMes)(Cl)2RuC(H)[(C6H 4)OCH(Me)(C(O)NMe2)] showed that the carbonyl oxygen of the amide and the terminal oxygen of the benzylidene ether are both coordinated to the metal to give an octahedral structure. However, the carbonyl oxygen of complexes (H2IMes)(Cl)2RuC(H)[(C6H 3X)OCH(CH2C(O)OCH2)(X = H, OMe)] does not coordinate to the metal due to the steric effect of the lactone. All these complexes were used as catalysts for olefin metathesis reactions and all exhibited excellent performances for the ring-closing metathesis (RCM) of diethyl diallymalonate at 30 C. The initiation rate of these catalysts was higher than that for the Hoveyda catalyst ((H2IMes)(Cl) 2RuC(H)(C6H4-2-OiPr)) and these complexes are also active for cross metathesis (CM).

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium. In my other articles, you can also check out more blogs about 246047-72-3

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

Reference of 15746-57-3, An article , which mentions 15746-57-3, molecular formula is C20H16Cl2N4Ru. The compound – Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II) played an important role in people’s production and life.

An electrochemical luminescent probe ruthenium – CBT and its preparation method and application (by machine translation)

The invention discloses an electrochemical luminescent probe ruthenium – CBT and its preparation method and application, relates to the field of biological detection technique. The method is introduced on the CABT active amino, get active amino – CBT, used for modification to the terpyridyl in ruthenium; through amino, carboxyl dehydration condensation role will be active amino – CBT Ru (bpy) modified to3 2 + The upper, electrochemical light-emitting probe by the Ru (bpy)3 2 + – CBT. The method of this invention is more simple and rapid, and the versatility is good, for the detection of different target protease, by replacing the corresponding polypeptide substrate sequence, can realize the detection of different protease, wide application range, proteinase detection specificity is good, high sensitivity. Probe design is simple, the operation step is short, easy in scientific research and clinical diagnosis field popularization and application; detection strategy is simple, without special material modification and processing requirements. (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

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.10049-08-8, Name is Ruthenium(III) chloride, molecular formula is Cl3Ru. In a Article£¬once mentioned of 10049-08-8, Recommanded Product: Ruthenium(III) chloride

Chemical and light-driven oxidation of water catalyzed by an efficient dinuclear ruthenium complex

Here splits the sun: A dinuclear ruthenium complex has been synthesized and employed to catalyze the homogeneous water oxidation (see picture; purple Ru, green Cl, blue N, red O). An exceptionally high turnover number was observed both for chemical (CeIV as the oxidant) and light-driven ([Ru(bpy)3]2+-type photosensitizers) water splitting.

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.Recommanded Product: Ruthenium(III) chloride, you can also check out more blogs about10049-08-8

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

Application of 32993-05-8, An article , which mentions 32993-05-8, molecular formula is C41H35ClP2Ru. The compound – Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II) played an important role in people’s production and life.

Some reactions of the ruthenium allenylidene complex [Ru(C=C=CPh2)(PPh3)2Cp][PF6] with nucleophiles

Reactions between [Ru(C=C=CPh2)(PPh3)2Cp][PF6] and nucleophilic reagents LiMe, NaOMe, KCN and KC5H5 have given the neutral substituted alkynyl-ruthenium complexes Ru{CCCPh2(Nu)}(PPh3)2Cp. The molecular structures of complexes with Nu=OMe, CN and C5H5 have been determined.

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

10049-08-8, Name is Ruthenium(III) chloride, molecular formula is Cl3Ru, belongs to ruthenium-catalysts compound, is a common compound. In a patnet, once mentioned the new application about 10049-08-8, SDS of cas: 10049-08-8

KINETICS AND MECHANISM OF RUTHENIUM(III)-CATALYSED OXIDATION OF ALLYL ALCOHOL BY MOLECULAR OXYGEN.

Oxidation of allyl alcohol by molecular oxygen catalysed by ruthenium(III) chloride in the pH range 1. 0 – 3. 0 is reported. The kinetics of the reaction, in the pH range 1. 0 – 2. 0, indicate a first-order dependence on ruthenium(III) ion and allyl alcohol concentrations and a zero-order dependence with respect to molecular oxygen concentration. The rate of oxidation was also found to be directly proportional to the hydrogen ion concentration. In the pH range 2. 0 – 3. 0, the rate of oxidation of allyl alcohol was found to be first order with respect to ruthenium(III) ion, first order with respect to allyl alcohol, and inversely proportional to hydrogen ion concentration.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 10049-08-8. In my other articles, you can also check out more blogs about 10049-08-8

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

Electric Literature of 246047-72-3. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 246047-72-3, Name is (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium

Potent inhibitors of hepatitis C core dimerization as new leads for anti-hepatitis C agents

New indoline alkaloid-type compounds which inhibit HCV production by infected hepatoma cells have been identified. These compounds, dimeric-type compounds of previously known inhibitors, display double digit nanomolar IC 50 and EC50 values, with cytotoxicity CC50 indexes higher than 36 muM, thus providing ample therapeutic windows for further development of HCV drugs.

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

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, Formula: C20H16Cl2N4Ru

Binding of 9-Methylguanine to [cis-Ru(2,2?-bpy)2] 2+: First X-ray Structure of a cis-Bis Purine Complex of Ruthenium

Reaction of [cis-Ru(2,2?-bpy)2(O3SCF 3)2] (1) with 9-methylguanine (9-MeG) affords the cis-[Ru(2,2?-bpy)2(9-MeG)2]2+ complex (2) in good yield. Two bases bind to the metal center via the N7 atoms. X-ray structure analysis of 2(SO3CF3)2 (monoclinic, P21/n, a = 12.5159(6) A, b = 20.0904(13) A, c = 17.1202(9) A, beta = 98.981(6), V= 4252.1(4) A3, Z = 4) reveals that the two bases are in a head-to-tail (HT) orientation with base-base dihedral angle of 60.4. NMR studies confirm that the complex is stable in water for hours, and no evidence for guanine substitution by solvent molecules was found.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C20H16Cl2N4Ru. In my other articles, you can also check out more blogs about 15746-57-3

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