Tìm thấy 12+ kết quả cho từ khóa "Transition metal complexes"
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There are many complexes of the type [ Cp 2 ML n ] (n = 1, 3), where M is a transition metal towards the left of the periodic classification (M = Ti, V, Zr, Hf, Mo, for example). The t 2g orbitals of the metal therefore contribute partially to the occupied MO. of the complex [ W(Cl) 6 ] in an octahedral geometry contrasts strikingly with the instability of [ W(Me) 6 ] in this same geometry. (b) give the shape and the occupation of the π-type MO;.
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There are many complexes of the type [ Cp 2 ML n ] (n = 1, 3), where M is a transition metal towards the left of the periodic classification (M = Ti, V, Zr, Hf, Mo, for example). The t 2g orbitals of the metal therefore contribute partially to the occupied MO. of the complex [ W(Cl) 6 ] in an octahedral geometry contrasts strikingly with the instability of [ W(Me) 6 ] in this same geometry. (b) give the shape and the occupation of the π-type MO;.
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In spite of the extensive scientific literature on Schiff base metal complexes with indole moiety, not much is known about bicompartmental Schiff bases derived from indole moiety and their metal complexes. Melting points of the newly synthesized metal complexes were above 300 ◦ C.
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Molar conductance of the transition metal complexes was determined in DMF at room temperature by using an IQ Scientific Instruments Multimeter.. After the addition, the pH of the solution fell to 3.5 and was adjusted with 0.1 N NaOH in EtOH to 4.5–5.0 where the precipitation of the complex started. Copper(II)chloride hexahydrate (0.024 g, 0.174 mmol) dissolved in MeOH (15 mL) was added to a hot solution of the azo-oxime ligand (0.1 g, 0.35 mmol)) dissolved in MeOH (20 mL).
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Since all of the synthesized complexes were obtained as solids and since they did not crystallize properly, they were characterized spectroscopically.. Synthesis of the transition metal complexes 6–20..
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The magnetic susceptibility results of transition metal complexes give an indication of the geometry of the ligands around the central metal ion. The magnetic moment of the Ni(II) complex (3) is 3.37 B.M., which is in good agreement with a d 8 system in a tetrahedral environment.
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Most of such oxidation reactions are still via homogeneous catalysts, but deactivation of the catalyst by self-aggregation of active sites, high cost, and lack of recycling make them inappropriate for large-scale applications. 3 Encapsu- lation of transition metal complexes in zeolite leads to transition metal complex molecules being encaged and site-isolated, and this can enhance the selectivity, activity, reusability, thermal, and chemical stability of the catalyst.
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The results obtained from the cytotoxicity experiments are especially promising for further research, which must be carried out for the evaluation of the studied complexes as anticancer drugs.. 2 This is also true for metal-containing drugs because of the metal-binding sites on DNA. 5 In the present study the drug efficiencies of the transition metal complexes of two different oxime ligands were evaluated as a result of their interactions with DNA.
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In the pH = 6 ÷ 7 environment, the QBr, MeQBr 10 µM aqueous solutions can not detect the metal ions.. Table 3.36. Value IC 50 (µM) of the sample on cell lines. The results are shown in Table 3.37.. Table 3.37: Antimicrobial resistance test results of complexes. Table 3.36: Antimicrobial resistance test results of complexes. can see the complex elements of the rare earth element with ligands QBr, MeQBr are more resistant to Lactobacillus fermentum and Bacillus subtilis..
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“Nickel(II) complexes of p-[N, N – bis (2 – chloroethyl)amino] bendehyde – 4 – methylthiosemicarbazone: Synthesis, structural characterization and biological application”, Polyhedron, 50, pp. (1975), “Transition metal complexes of thiosemicarbazide and thiosemicarbazones” Coordination Chemistry Reviews, 15(2-3), pp..
01050001778.pdf
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“Thiosemicarbazide as an inhibitor for the acid corrosion of iron”, Corrosion Science, 16(3), pp.163-169.. (1975), “Transition metal complexes of thiosemicarbazide and thiosemicarbazones” Coordination Chemistry Reviews, 15(2-3), pp.279-319.. (1960), "The crystal structure of mono thiosemicarbazide zinc chloride", Acta crystallorg., 13, pp.688-698.. (1999), “Polystyrene-supported thiosemicarbazone- transition metal complexes: synthesis and application as heterogeneous catalysts”, Polimer International
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Chem), 535, pp.235-246.. (1976), “Thiosemicarbazide as an inhibitor for the acid corrosion of iron”, Corrosion Science, 16(3), pp.163-169.. (1975), “Transition metal complexes of thiosemicarbazide and thiosemicarbazones” Coordination Chemistry Reviews, 15(2-3), pp.279-319..
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Therefore, to obtain elaborate physical properties and stability on metal complexes, chemical modification of the ligand is one of the most promising strategies. In this method, the replacement of -system of the benzene ring to. -expanded aromatic rings induces drastic change in the properties of the resultant complexes [21].. Salicylaldimine is one type of the Schiff base ligands containing an NO chelate binding for complexation with most of the transition metals such as Pt 2.
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XRD data of the [Mn(mb) 2 (H 2 O) 2 ].4H 2 O metal complex.. XRD data of the [Co(mb) 2 (H 2 O) 2 ].8H 2 O metal complex.. XRD parameters of the mbH ligand and its metal complexes.. All complexes show strong cathodic peaks in the range from –0.5 to 1.0 V. The complexes have 2 anodic peaks in the 1.4–2.0 V range. The complexes show irreversible cathodic peak potentials in the 1.0–1.4 V range..
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The electronic spectra of the metal. complexes displayed strong bands in the range of 350–381 nm, which can be assigned to n → π*, and a charge transfer LMCT band was exhibited in the range of 400–410 nm. On the other hand, the spectra of metal complexes displayed bands in the visible region observed at 422–468 nm, which are assigned to d–d electronic transition.
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According to the spectral data of the new metal complexes obtained, both metal complexes are in the monoclinic crystal system and in the P2 1 /c and P2 1 space groups, respectively..
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The extraction power of some reagents was determined for the heavy metal extraction from biofilm samples collected in Erdemli coast in the Mediterranean Sea. The concentration and pH of the ammonium acetate solution were optimized and found as 1 M and 5, respectively. The chromatograms of metal complexes with the C-18-HPLC-ICP-MS system were taken to determine the effect of the pH of the metal complexes.
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The compound was crystalline in nature and was soluble in common organic solvents. stoichiometry of the complexes. The observed IR, 1 H NMR, and mass spectral data were in conformity with structure 1 (Figure 1) of H 2 L and structure 2 (Figure 2) of the complexes.. Structure of the metal complexes of H 2 L..
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However, by performing a double-condensation reaction in the presence of transition metal ions having template effect and a second carbonyl molecule, thiosemicarbazone-metal complexes with tetradentate coordination can be obtained [8–10].
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Since the isolation of the first free carbene by Arduengo, 1 transition metal carbene complexes have found wide application in organometallic chemistry. 2 − 8 NHC–Ag(I) complexes have particular importance due to their structural variations and wide applications as op- erative NHC transfer agents in transmetalation reactions to make other NHC–metal complexes. 9 − 15 The notice- able biological activity of NHC–silver complexes as anticancer and antimicrobial agents has been confirmed. 16 − 22 In spite