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A Ruthenium(II) Complex as a Luminescent Probe for DNA Mismatches and Abasic Sites

[Ru(bpy)2(BNIQ)]2+ (BNIQ = Benzo[c][1,7]naphthyridine-1-isoquinoline), which incorporates the sterically expansive BNIQ ligand, is a highly selective luminescent probe for DNA mismatches and abasic sites, possessing a 500-fold higher binding affinity toward these destabilized regions relative to well-matched base pairs. As a result of this higher binding affinity, the complex exhibits an enhanced steady-state emission in the presence of DNA duplexes containing a single base mismatch or abasic site compared to fully well-matched DNA. Luminescence quenching experiments with Cu(phen)22+ and [Fe(CN)6]3- implicate binding of the complex to a mismatch from the minor groove via metalloinsertion. The emission response of the complex to different single base mismatches, binding preferentially to the more destabilized mismatches, is also consistent with binding by metalloinsertion. This work shows that high selectivity toward destabilized regions in duplex DNA can be achieved through the rational design of a complex with a sterically expansive aromatic ligand.

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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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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., Safety of Dichloro(benzene)ruthenium(II) dimer

New ruthenium(II)-letrozole complexes as anticancer therapeutics

Novel ruthenium-letrozole complexes have been prepared, and cell viability of two human cancer cell types (breast and glioblastoma) was determined. Some ruthenium compounds are known for their cytotoxicity to cancer cells, whereas letrozole is an aromatase inhibitor administered after surgery to post-menopausal women with hormonally responsive breast cancer. A significant in vitro activity was established for complex 5¡¤Let against breast cancer MCF-7 cells and significantly lower activity against glioblastoma U251N cells. The activity of 5¡¤Let was even higher than that of 4, a compound analogous to the well-known drug RAPTA-C. Results from the combination of 5¡¤Let (or 4) with 3-methyladenine (3-MA) or with curcumin, respectively, revealed that the resultant cancer cell death likely involves 5¡¤Let-induced autophagy.

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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 14564-35-3 is helpful to your research., COA of Formula: C38H34Cl2O2P2Ru

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14564-35-3, Name is Dichlorodicarbonylbis(triphenylphosphine)ruthenium(II), molecular formula is C38H34Cl2O2P2Ru. In a Article£¬once mentioned of 14564-35-3, COA of Formula: C38H34Cl2O2P2Ru

REACTIONS OF A DICHLOROCARBENE-RUTHENIUM COMPLEX, RuCl2(CCl2)(CO)(PPh3)2

The dichlorocarbene ligand, in the new complex RuCl2(CCl2)(CO)(PPh3)2, readily undergoes substitution reactions in which the integrity of the metal-carbon bond is maintained.Reactions with species H2X (X=O, S, Se) give chalcocarbonyl complexes RuCl2(CX)(CO)(PPh3)2 while RXH (X=O, S) give new carbene complexes RuCl2(CO)(PPh3)2.Ammonia reacts to give a cyanide-containing complex, RuCl(CN)(CO)(NH3)(PPh3)2, and primary amines, an isocyanide complex, or in the case of certain primary diamines cyclic carbene complexes.RuCl2(CNNMe2)(CO)(PPh3)2 is formed in the reaction with N,N-dimethylhydrazine.Secondary amines, R2NH, react to give chloroaminocarbene complexes, RuCl2(CO)(PPh3)2.

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

New explortion of 301224-40-8

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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 Article£¬once mentioned of 301224-40-8, Quality Control of: (1,3-Dimesitylimidazolidin-2-ylidene)(2-isopropoxybenzylidene)ruthenium(VI) chloride

Kinetic selectivity of olefin metathesis catalysts bearing cyclic (alkyl)(amino)carbenes

The evaluation of ruthenium olefin metathesis catalysts 4-6 bearing cyclic (alkyl)(amino)carbenes (CAACs) in the cross-metathesis of cis-1,4-diacetoxy-2- butene (7) with allylbenzene (8) and the ethenolysis of methyl oleate (11) is reported. Relative to most NHC-substituted complexes, CAAC-substituted catalysts exhibit lower E/Z ratios (3:1 at 70% conversion) in the cross-metathesis of 7 and 8. Additionally, complexes 4-6 demonstrate good selectivity for the formation of terminal olefins versus internal olefins in the ethenolysis of 11. Indeed, complex 6 achieved 35 000 TONs, the highest recorded to date. CAAC-substituted complexes exhibit markedly different kinetic selectivity than most NHC-substituted complexes.

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

New explortion of 32993-05-8

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II). In my other articles, you can also check out more blogs about 32993-05-8

32993-05-8, Name is Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II), molecular formula is C41H35ClP2Ru, belongs to ruthenium-catalysts compound, is a common compound. In a patnet, once mentioned the new application about 32993-05-8, Quality Control of: Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)

DISUBSTITUTED VINYLIDENE COMPLEXES OF IRON AND RUTHENIUM: NUCLEOPHILIC PROPERTIES OF eta1-ACETYLIDE LIGANDS

The eta1-acetylide complexes (C5H5)ML2(C<*>CR) (M=Fe, Ru; L=PPh3, L2=Ph2PCH2CH2PPh2) are nucleophilic at the beta-carbon and react with a variety of mild electrophiles to yield the corresponding disubstituted vinylidene complexes <(C5H5)ML2(=C=CRR')>PF6.

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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: 37366-09-9

Reactions of the Lithiated Diphosphine tBu2P?P(SiMe3)Li with [(eta6-C6H6)RuCl2]2in the Presence of Tertiary Phosphines

tBu2P?P(SiMe3)Li reacted with [(eta6-C6H6)RuCl2]2at ?40 C in the presence of PR3(PR3= PEt3, PEt2Ph, PEtPh2) by the nucleophilic addition of the tBu2P?P(SiMe3) moiety to the benzene ring to yield solely the complexes [(R3P)2Ru(Cl){eta5-C6H6(Me3SiP?PtBu2)}] (1). These products decomposed slowly at ambient temperature to yield benzene, Ru clusters, and small amounts of the dinuclear ruthenium complexes [{(R3P)2Ru}2(mu,eta2:2-P2)2Ru(PR3)2] (Ru?Ru) (6). Single-crystal X-ray diffraction studies of [(PhEt2P)2Ru(Cl){eta5-C6H6(Me3SiP?PtBu2)}] (1b) and [(Ph2EtP)2Ru(Cl){eta5-C6H6(Me3SiP?PtBu2)}] (1c) revealed that the addition of the tBu2P?P(SiMe3) group occurred through an exo pathway. Complex 6a (R = Et) displays a planar rectangular P4system consisting of two P2units and a Ru?Ru distance that lies in the range of a single bond.

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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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Nitrosyl ruthenium complexes with general formula [RuCl3(NO)(P-P)] (P-P = {PPh2(CH2)nPPh2}, n = 1-3 and {PPh2-CH = CH-PPh2}). X-ray structure of [RuCl3(NO){PPh2(CH2)3PPh 2}]

Ruthenium(II) complexes with general formula [RuCl3(NO)(P-P)] were obtained in the solid state, where P-P = PPh2(CH2)nPPh2 (n = 1-3) and PPh2-CH = CH-PPh2. The 31P NMR spectra of these compounds measured in CH2Cl2 showed only singlets, consistent with a fac configuration containing two equivalent phosphorus atoms. However the X-ray diffraction data show that the [RuCl3(NO){PPh2(CH2)3PPh 2}] complex crystallizes in a mer configuration, where one of the phosphorus atoms is trans to the NO group, in a slightly distorted octahedral geometry. 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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Novel mononuclear eta5-pentamethylcyclopentadienyl complexes of platinum group metals bearing pyrazolylpyridazine ligands: Syntheses and spectral studies

Condensation of 3,6-dichloropyridazine with 3,5-dimethylpyrazole in 1:1 ratio yielded one side substituted pyrazolylpyridazine ligand 3-chloro-6-(3,5-dimethylpyrazolyl)pyridazine (L) while condensation of 3,6-dichloropyridazine with substituted pyrazoles in 1:2 ratio yielded both side substituted pyrazolylpyridazine ligands such as 3,6-bis(pyrazolyl)pyridazine (L1), 3,6-bis(3-methylpyrazolyl)pyridazine (L2) and 3,6-bis(3,5- dimethylpyrazolyl)pyridazine (L3). A new series of cationic mononuclear complexes of the type [(eta5-Cp)Ma(L)(PPh3)]PF6, [(eta5-Cp)Mb(L)Cl]PF6, [(eta5-Cp)Ru(L?)(PPh3)]PF6and [(eta5-Cp)Mb(L?)Cl]+(where Ma= Ru, Os; Mb= Rh, Ir and L? = L1, L2, L3) bearing pyrazolylpyridazine and eta5-cyclopentadienyl ligands are reported. The complexes have been completely characterized by spectral studies. The molecular structures of representative complexes have been determined by single crystal X-ray crystallography.

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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.COA 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, COA of Formula: C20H16Cl2N4Ru

Near-IR phosphorescent ruthenium(II) and iridium(III) perylene bisimide metal complexes

The phosphorescence emission of perylene bisimide derivatives has been rarely reported. Two novel ruthenium(II) and iridium(III) complexes of an azabenz-annulated perylene bisimide (ab-PBI), [Ru(bpy)2(ab-PBI)][PF6]2 1 and [CpIr-(ab-PBI)Cl]PF6 2 are now presented that both show NIR phosphorescence between 750-1000 nm in solution at room temperature. For an NIR emitter, the ruthenium complex 1 displays an unusually high quantum yield (Fp) of 11% with a lifetime (tp) of 4.2 ms, while iridium complex 2 exhibits Fp < 1% and tp =33 ms. 1 and 2 are the first PBI-metal complexes in which the spin-orbit coupling is strong enough to facilitate not only the Sn?Tn intersystem crossing of the PBI dye, but also the radiative T1?S0 transition, that is, phosphorescence. Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.COA of 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

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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.

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