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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.COA of Formula: C20H16Cl2N4Ru

Ln2M complexes (M = Ru, Re) derived from a bismacrocyclic ligand containing a 4,4?-dimethyl-2,2?-bipyridyl bridging unit

Homodinuclear lanthanide complexes derived from a ligand featuring two DO3A chelating sites linked by a 4,4?-dimethyl-2,2?-bipyridyl spacer were prepared and characterized. The bipyridyl coordination site of 1 was used to introduce Ru(Bpy)2 and Re(CO)3Cl moieties, leading to the formation of heterometallic d-f2 complexes with general formulae [Ln2¡¤1¡¤Ru(Bpy)2]2+ (Ln = Nd, Eu, Tb, Yb and Lu) and [Ln2¡¤1¡¤Re(CO)3Cl] (Ln = Nd, Yb and Lu). The luminescence properties of the complexes were investigated by means of absorption spectroscopy and steady-state and time-resolved luminescence spectroscopy covering the visible and NIR regions. Both Ru and Re chromophores were shown to act as efficient sensitizers of the NIR emission of Yb and Nd in aqueous solutions. We also consider the unsaturated coordination spheres of the Ln cations in the Ln2¡¤1 complexes, which form ternary complexes with bidentate anions without showing particular synergistic effects for polyanionic species.

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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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Receptor selective ruthenium-somatostatin photosensitizer for cancer targeted photodynamic applications

The efficient conjugation of a ruthenium complex and the peptide hormone somatostatin is presented. The resultant biohybrid offers valuable features for photodynamic therapy such as remarkable cellular selectivity, rapid cell uptake by receptor-mediated endocytosis, efficient generation of 1O2 upon irradiation, potent phototoxicity as well as low cytotoxicity in the “off”-state.

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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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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

SYNTHESIS OF TRIPLE HALIDE-BRIDGED ARENE COMPLEXES OF RUTHENIUM(II) AND OSMIUM(II)

Reaction of <2> (M = Ru; X = Cl-, Br-, I-; M = Os, X = Cl-) with C5H5N in methanol, followed by addition of NH4PF6 gives the monocations PF6.Treatment of an equimolar mixture of these compounds and the corresponding with HBF4 in methanol then provides a high yield synthesis of the triple halide-bridged complexes BF4.Spectroscopic evidence for the formation of heterobridged, heteroarene and heteronuclear triple halide-bridged arene complexes of ruthenium(II) and osmium(II) using this synthetic route is also discussed.

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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.category: ruthenium-catalysts. In my other articles, you can also check out more blogs about 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, category: ruthenium-catalysts.

Guanidinates as chelating anionic ligands for early, middle and late transition metals: Syntheses and crystal structures of [Ti{i]2(NPh)2CNEt2}2Cl2, [Ru{ii2-(NPh)2CNHPh}3] and [Pt{ri2-(NPh)2CNHPh}2]

Treatment of the dimeric ruthenium halide complex [Ru(r|-C6H6)Q2]2 with 1,2,3-triphenylguanidine provided the tris-chelate [Ru{r|2-(NPh)2CNHPh}3] with loss of the aromatic ligand and metal oxidation. This product may also be prepared by treatment of the previously reported [Ru(n-/>-PrrC6H4Me){ri2-(NPh)2CNHPh}Cl] with bases (KOH, LiN’Pr2, NEtj). Complexes containing chelating guanidinate ligands are also available by means of metathesis of the monolithiated ligands Li[C(NR)2NR2] with metal halide complexes, as exemplified by the synthesis of the square planar bis-chelate [Pt{n2-(NPh)2CNHPh}2] from [Pt(PhCN)2ClJ and [Ti{n2-(NPh)2CN(Et)2}2Cl2] from [TiCl4(THF)2]. The characterisation of these complexes allows a comparison of the co-ordination properties of chelating guanidinates with early, middle and late transition metals. The Royal Society of Chemistry 2000.

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

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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. 37366-09-9, C12H12Cl4Ru2. A document type is Article, introducing its new discovery., Application In Synthesis of Dichloro(benzene)ruthenium(II) dimer

Quinones synthesis via hydrogen peroxide oxidation of dihydroxy arenes catalyzed by homogeneous and macroporous-polymer-supported ruthenium catalysts

Ruthenium(II)/dimethyl phenyloxazoline (Ru(II)/dm-Pheox) complex 2a and its macroporous-polymeric-catalyst 4 were found to be very rapid and efficient catalysts in the hydrogen peroxide oxidation of 1,2- and 1,4-dihydroxy arenes. Most of the quinone products were delivered in 99% yield. The polymeric-catalyst 4 could be reused at least five times.

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

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The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 15746-57-3 is helpful to your research., Recommanded Product: Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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

A ruthenium(II) allenylidene complex with a 4,5-diazafluorene functional group: A new building-block for organometallic molecular assemblies

The synthesis of the new ruthenium(II) allenylidene complex [ClRu(dppe)2{double bond, long}C{double bond, long}C{double bond, long}C11H6N2][OTf] (4) (dppe = 1,2-bis(diphenylphosphino)ethane) terminated with a 4,5-diazafluorene ligand is reported. Further coordination of that metal allenylidene to ruthenium and rhenium moieties leads to the bimetallic adducts [ClRu(dppe)2{double bond, long}C{double bond, long}C{double bond, long}C11H6N2{Ru(bpy)2}][B(C6F5)4]3 (5a), [ClRu(dppe)2{double bond, long}C{double bond, long}C{double bond, long}C11H6N2{Ru(tBu-bpy)2}][PF6]3 (5b) and [ClRu(dppe)2{double bond, long}C{double bond, long}C{double bond, long}C11H6N2{Re(CO)3Cl}][OTf] (6). Their optical and electrochemical properties show that the allenylidene moiety is an attractive molecular clip for the access to larger original redox-active homo/heteronuclear multi-component supramolecular assemblies. The X-ray crystal structure of the allenylidene metal building block is also described.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 15746-57-3 is helpful to your research., Recommanded Product: Cis-Dichlorobis(2,2′-bipyridine)ruthenium(II)

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

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

Half sandwich complexes of chalcogenated pyridine based bi-(N, S/Se) and terdentate (N, S/Se, N) ligands with (eta6-benzene)ruthenium(ii): Synthesis, structure and catalysis of transfer hydrogenation of ketones and oxidation of alcohols

The half sandwich complexes [(eta6-C6H 6)Ru(L)Cl][PF6] (1-5) have been synthesized by the reactions of (2-arylchalcogenomethyl)pyridine [L = L1-L3] and bis(2-pyridylmethyl)chalcogenide [L = L4-L5] (chalcogen = S, Se; Ar = Ph/2-pyridyl for S, Ph for Se) with [(eta6-C6H 6)RuCl2]2, at room temperature followed by treatment with NH4PF6. Their HR-MS, 1H, 13C{1H} and 77Se{1H} NMR spectra have been found characteristic. The single crystal structures of 1-5 have been established by X-ray crystallography. The Ru has pseudo-octahedral half sandwich “piano-stool” geometry. The complexes 1-5 have been found efficient for catalytic oxidation of alcohols with N-methylmorpholine-N-oxide (NMO) and transfer hydrogenation of ketones with 2-propanol (at moderate temperature 80 C) as TON values are up to 9.9 ¡Á 103 and 9.8 ¡Á 103 respectively for the two catalytic reactions. On comparing the required catalyst loading for good conversions and reaction time for the present complexes with those reported in literature for other transfer hydrogenation/oxidation catalysts, it becomes apparent that 1-5 have good promise. The complexes of Se ligands have been found more efficient than their sulphur analogues. The complexes of bidentate ligands are more efficient than those of terdentate, due to difficult bond cleavage in the case of latter. These orders of efficiency are supported by DFT calculations. The calculated bond lengths/angles by DFT are generally consistent with the experimental ones.

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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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Facile synthesis of heterobimetallic [FeII(mu-diphosphine)RuII] and homobimetallic [FeII(mu-diphosphine)FeII] complexes and their in vitro cytotoxic activity on cisplatin-resistant cancer cells

A series of heterobimetallic [Fe,Ru] and homobimetallic [Fe,Fe] complexes, featuring mu -diphosphine bridges between the two metal centres, are reported along with their in vitro cytotoxicity activity on the A2780cisR cell-line. The known starting material [CpFe(CO)2(CH3)] (Cp = eta5-C5H5) (1) was reacted with dppe (1,2-bis(diphenylphosphino)ethane) forming the known mononuclear kappa1-dppe complex: [CpFe(CO)(COCH3)(kappa1-dppe)] (2) and the known dinuclear complex: and [[CpFe(CO)(COCH3)]2(mu-dppe)] (3). Dimer cleavage reactions between complex 2 and two ruthenium arene complexes [(eta6-p-cymene)RuCl2]2 and [(eta6-benzene)RuCl2]2 formed two new heterobimetallic complexes: [CpFe(CO)(COCH3)(mu-dppe)Ru(eta6-cymene)Cl2] (4) and [CpFe(CO)(COCH3)(mu-dppe)Ru(eta6-C6H6)Cl2] (5). A homobimetallic system, [[CpFe(CO)(I)]2(mu-dppb)] (6) was obtained by the facile reaction between of [CpFe(CO)2I] and 1,4-bis(diphenylphosphino)butane (dppb). Complex 6 was methylated using MeLi to generate the more lipophilic complex [[CpFe(CO)(CH3)]2(mu-dppb)] (7). All of the complexes were fully characterized by spectroscopy (1H, 13C {1H}, 31P {1H} NMR; FTIR, UV?Vis), and high resolution mass spectrometry (HRMS). Density functional theory calculations (DFT) (Level of theory B3LYP, basis set for H, C, P, O, Cl is 6-31+G(d,p) and for Ru, Fe, I is DGDZVP) on complexes 5 and 6 are also reported. An excellent agreement between the DFT calculated infra-red (IR) spectra of the optimised geometries of 5 and 6 was found with the experimentally determined spectra. In vitro cytotoxicity studies of all complexes was carried out on A2780cisR (cisplatin resistant ovarian cancer cell-line) and compared to cisplatin as a positive control and RAPTA-C as a negative control. Although limited to only one cell-line, the results show that the heterobimetallic complexes 4 and 5 are the most cytotoxic (IC50 = 4.9 ¡À 0.4 muM and 6.5 ¡À 0.1 muM respectively), whilst the dinculear [Fe,Fe] complexes exhibit no, or very low cytotoxicity.

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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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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

A novel […] complex and its preparation method and application (by machine translation)

The invention discloses a novel […] complex and its preparation method and application, the composition is formed by multi-bipyridine ligand, metal center and containing donor functional group of auxiliary ligand, the complex in the donor group to the electronic capacity is strong, oxidation potential is low, is strong, lose the electronic capacity; for electronic ring metallized C ^ N ligand dp (Ru) improve the track level, electronic transfer capacity is improved substantially, the invention synthetic ruthenium biological toxicity is low, can be used for the hypoxic environment of the I-type photodynamic therapy, photodynamic therapy effect is improved, the optical power in the treatment of important application prospect; and this kind of compound the synthetic method is simple, mild synthetic conditions, and is suitable for mass production and use. (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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Aminooxazolinate; a chiral amidinate analogue

High levels of diastereoselection with respect to chirality-at-metal are achieved at equilibrium for complexes containing a new and available range of diazaallyl ligands.

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