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Related Products of 3153-26-2, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 3153-26-2, Name is Vanadyl acetylacetonate,introducing its new discovery.

[VO(acac)2] reacts with HL (HL is the hydrazone Hacpy-inh I, or Hacpy-bhz II; acpy = acetylpyridine, inh = isonicotinic acid hydrazide, bhz = benzoylhydrazide) in dry methanol to yield the oxovanadium(IV) complexes [VOL(acac)] (HL = I: 1, HL = II: 3). The dioxovanadium(v) complexes [VO2L] (HL = I: 2, HL = II: 4) are obtained by aerial oxidation of 1 and 3 in methanol. Treatment of 1 and 3, or 2 and 4, with H2O2 yields the oxoperoxovanadium(v) complexes [VO(O2)L] (HL = I: 5, HL = II: 6). In the presence of catechol or benzohydroxamic acid, 1 and 3 give the mixed chelate complexes [VOL(cat)] (HL = I: 7, HL = II: 8) or [VOL(bha)] (HL = I: 9, HL = II: 10). The peroxo complexes 5 and 6 undergo oxygen transfer reaction with PPh3 in DMF. In DMF and DMSO, 7, 8, 9 and 10 slowly convert to the corresponding dioxo species 2 and 4. Acidification of 2 and 4 with HCl dissolved in methanol affords oxo-hydroxo complexes. Reaction of 7 with L-ascorbic acid yields 2. The crystal and molecular structures of 2 and 4 have been determined, confirming the ONN binding mode of I and II from their enolate form.

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Eight alkali metal ion-mediated dioxidovanadium(v), [{VVO 2L1-6}A(H2O)n]?, complexes for A = Li+, Na+, K+ and Cs +, containing tridentate aroylhydrazonate ligands coordinating via ONO donor atoms, are described. All the synthesised ligands and the metal complexes were successfully characterised by elemental analysis, IR, UV-Vis and NMR spectroscopy. X-ray crystallographic investigation of 3, 5-7 shows the presence of distorted NO4 coordination geometries for LVO 2- in each case, and varying mu-oxido and/or mu-aqua bridging with interesting variations correlated with the size of the alkali metal ions: with small Li+, no bridging-O is found but four ion aggregates are found with Na+, chains for K+ and finally, layers for Cs+. Two (5) or three-dimensional (3, 6 and 7) architectures are consolidated by hydrogen bonding. The dioxidovanadium(v) complexes were found to exhibit DNA binding activity due to their interaction with CT-DNA by the groove binding mode, with binding constants ranging from 103 to 104 M-1. Complexes 1-8 were also tested for DNA nuclease activity against pUC19 plasmid DNA which showed that 6 and 7 had the best DNA binding and photonuclease activity; these results support their good protein binding and cleavage activity with binding constants ranging from 104 to 105 M-1. Finally, the in vitro antiproliferative activity of all complexes was assayed against the HeLa cell line. Some of the complexes (2, 5, 6 and 7) show considerable activity compared to commonly used chemotherapeutic drugs. The variation in cytotoxicity of the complexes is influenced by the various functional groups attached to the aroylhydrazone derivative.

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Metal catalyst and ligand design,
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New oxidovanadium(V) complexes, [VOL1(bzh))]·H2O (1) and [VOL2(bzh))] (2), were prepared by the reaction of [VO(acac)2] (where acac = acetylacetonate) and benzohydroxamic acid (Hbzh) with N?-(5-bromo-2-hydroxybenzylidene)-3-methylbenzohydrazide (H2L1) and N?-(5-bromo-2-hydroxybenzylidene)- 4-methylbenzohydrazide (H2L2), respectively, in methanol. Structures of the complexes were determined by elemental analysis, infrared and UV?vis spectra. Single crystal structures of the complexes were determined by X-ray diffraction. Vanadiums have octahedral coordination. Thermal stability and the inhibition of urease of the complexes were studied.

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Metal catalyst and ligand design,
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Reference of 3153-26-2, In heterogeneous catalysis, the catalyst is in a different phase from the reactants. At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 3153-26-2, name is Vanadyl acetylacetonate. In an article,Which mentioned a new discovery about 3153-26-2

Some new oxovanadium(V) complexes, [VOL1-3(OEt)(EtOH)] (1-3), have been reported, which were obtained from the reaction of the Schiff bases H2L1-3 (where H2L1 = the salicylhydrazone of diacetyl monoxime; H2L2 = the 4-methoxy salicylhydrazone of diacetyl monoxime and H2L3 = the 4-hydroxy salicylhydrazone of diacetyl monoxime) with VO(acac)2 in a 1:1 molar ratio. Three 4-R-aroylhydrazoneoximes (V) have been used as ligands in the present study, differing in the inductive effect of the substituent R (R = H, OCH3 and OH), in order to observe their influence, if any, on the redox potentials and biological activity of the complexes. All the synthesized ligands and metal complexes were successfully characterized by elemental analysis, IR, UV-Vis and NMR spectroscopy. An X-ray diffraction study of [VOL1(OEt)(EtOH)] (1) reveals that the metal center has a distorted octahedral O5N coordination sphere, where the O,N,O donor ligand and the ethoxo group constitute a satisfactory O3N basal plane. Cyclic voltammetry of the complexes show a quasi-reversible cyclic voltammetric response in the potential range 0.29-0.36 V involving a single electron V(V)-V(IV) reduction. The complexes have also been screened for their antibacterial activity against Escherichia coli, Bacillus, Proteus and Klebsiella. Minimum inhibitory concentrations of these complexes and the antibacterial activities indicate compound 1 as the potential lead molecule for drug design.

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Metal catalyst and ligand design,
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The selective epoxidation of olefinic alcohols with t-BuOOH in the presence of vanadium catalysts proceeds in liquid carbon dioxide with high conversions and selectivities. Rates measured in liquid CO2 for the oxovanadium(V) triisopropoxide catalyzed epoxidation of allylic and homoallylic alcohols using tert-butyl hydroperoxide are comparable to those measured in methylene chloride, toluene, and n-hexane. The reactivity of the vanadium(IV) bis(acetylacetonato) oxide catalyst in liquid CO2 was found to be substantially lower than in organic solvents, presumably due to its low solubility in C02. Highly fluorinated acac-type ligands increased the catalytic reactivity of VO(acac)2-catalyzed epoxidations by enhancing catalyst precursor solubility. Heterogeneous epoxidation reactions were also carried out in liquid CO2 using vanadium complexes supported on cation-exchange polymers.

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Reaction of 2-acetylpyridine semicarbazone (H2APS), 3-acetylpyridine semicarbazone (H3APS) and 4-acetylpyridine semicarbazone (H4APS) with [VO(acac)2] (acac = acetylacetonate) gave [VO(H2APS)(acac)2] (1), [VO(H3APS)(acac)2] (2) and [VO(4APS)(acac)(H2O)] · 1/2H2O (3). Oxidation of complex 1 in acetonitrile gave [VO2(2APS)] (4). The crystal structures of complexes 1 and 4 have been determined. Complexes 1-3 were able to enhance glucose uptake and to inhibit glycerol release from adipocytes, which indicate their potential to act as insulin-mimics.

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Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 3153-26-2, molcular formula is C10H14O5V, introducing its new discovery. Quality Control of: Vanadyl acetylacetonate

Three new mononuclear Schiff base complexes [Co(L1)3 (1), VO(L1)2 (2) and Cu(L2)2 (3)] were synthesized, characterized and used as a precursor for preparation of metal oxide nanoparticles. The crystal structure of compounds was determined using single crystal X-ray diffraction. The Co(III) coordination sphere consists of three phenolato oxygens and three imino nitrogen atoms from three Schiff base ligands, thus forming a distorted octahedral geometry. In complex (2), the vanadium(IV) is five-coordinated in a regular tetragonal pyramid fashion and the Cu(II) ion is four coordinated with a square-planar geometry in the complex (3). The nanoparticles were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). In vitro cell proliferation via MTT assay was studied to calculate the cytotoxicity of complexes and metal oxide nanoparticles against gastric cancer cell line (MKN-45). The results showed that all compounds have anticancer activity with dose?response dependency.

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Metal catalyst and ligand design,
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Reaction of VO(acac)2 with N’-(3-bromo-5-chloro-2-hydroxybenzylidene)-3-methylbenzohydrazide (H2L) in methanol afforded a new mononuclear vanadium(V) complex, [VOL(OMe)(MeOH)]. Structure of the complex has been characterized by physico-chemical methods and single-crystal X-ray diffraction. The complex crystallizes as the monoclinic space group P21/c, with unit cell dimensions a = 13.1345(10) A, b = 18.6279(14) A, c = 7.8983(8) A, beta = 90.248(2), V = 1932.4(3) A3, Z = 4, R1 = 0.0963, wR2 = 0.2213, S = 1.113. X-ray analysis indicated that the V atom in the complex is in octahedral coordination. The insulin-like activity of the complex was studied, which can stimulate glucose uptake with 2-DOG uptake value of 0.81 nmol/3 min.

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Metal catalyst and ligand design,
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The authors report that in soluble metal complex-catalysed autoxidations of car-3-ene, a linear relationship is observed between the oxidation potentials (Eox) of the complexes and their rates of oxidation by car-3-ene-5 hydroperoxide. To the authors’ knowledge, this is the first time a definite relationship has been demonstrated between the redox potentials of catalysts and the rates of hydroperoxide decomposition. The overall oxidation process is considered to consist of several reaction steps. For the complexes presented, certain rate constants are estimated. A number of other complexes fail to show appreciable catalytic activities under the conditions employed (27C, 30 p.s.i. oxygen, carene: catalyst molar ratio = 100:1), or are insoluble (e.g. Co(stearate)2·2H2O) in the solvent (CH3CN) used for the electrochemical measurements.

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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 3153-26-2 is helpful to your research. COA of Formula: C10H14O5V

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 3153-26-2, name is Vanadyl acetylacetonate, introducing its new discovery. COA of Formula: C10H14O5V

Two oxovanadium(V) complexes, [VO(L)(L1)] (I) and [VOLL2] (II), where L = acetohydroxamate, H2L1 = 2-bromo-N’-(2-hydroxybenzylidene)benzohydrazide, H2L2 = 2-chloro-N’-(2-hydroxybenzylidene)benzohydrazide,have been synthesized by reaction of VO(Acac)2 with acetohydroxamic acid and hydrazone ligands, and characterized by elemental analyses, IR, UV-Vis, 1H NMR, molar conductivity, and X-ray single crystal structural determination (CIF file CCDC nos. 1911887 (I), 1911888 (II)). The hydrazone ligands coordinate to the V atoms through phenolate oxygen, imino nitrogen, and enolate oxygen atoms. The acetohydroxamate ligand coordinate to the V atoms through the two oxygen atoms. The V atoms are in octahedral coordination with the sixth site coordinated by an oxo group. The antibacterial property of the complexes and the hydrazones against the bacteria B. subtilis, E. coli, P. putida, and S. aureus were studied. Both complexes exhibit remarkable antibacterial properties on B. subtilis and S. aureus comparable to Penicillin.

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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI