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101.
A simple method is described for the separation of molybdenum from titanium, zirconium, chromium, manganese, iron, cobalt, nickel, uranium and aluminium in a wide variety of samples in <30 min. Phosphomolybdenum blue is produced by boiling for 2 min a molybdate solution containing phosphate to give Mo/P = 20-37 (w/w) with hydrazine sulphate in 0.1N sulphuric acid. The volume and acidity are adjusted to give a molybdenum concentration of 0.6-5 my/ml in 0.4-0.5N sulphuric acid. The phosphomolybdenum blue is 99.5% extracted with methyl isobutyl ketone in a single extraction. The residual molybdenum and hydrazine in the aqueous phase are oxidized with a few drops of liquid bromine and the molybdenum is quantitatively extracted with the same solvent from 1N sulphuric acid as its reddish brown thiosulphato complex. The molybdenum is stripped by ammonia-hydrogen peroxide solution. The back-extract is heated to boiling and filtered to remove the insoluble hydroxides of traces of accompanying elements. The thiosulphate in the filtrate is destroyed by boiling for 4-5 min with excess of hydrogen peroxide in slightly ammoniacal medium. The molybdenum is determined finally by cerimetry or other standard methods. 相似文献
102.
Highly enantioselective copper(I)-fesulphos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides
Cabrera S Gómez Arrayás R Carretero JC 《Journal of the American Chemical Society》2005,127(47):16394-16395
The catalyst system formed by Cu(CH3CN)4ClO4 and the planar chiral P,S-ligand Fesulphos behaves as a very efficient chiral Lewis acid in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides. This catalyst shows a remarkable reactivity at low catalyst loading (0.5-3 mol %), affording in good yields the endo adducts with exceptional levels of enantioselectivity (up to >99% ee). This catalytic asymmetric procedure has a broad structural scope with regard to both azomethine and dipolarophile substitution. The first examples of catalytic asymmetric 1,3-dipolar cycloaddition with ketimine-derived azomethines are reported. 相似文献
103.
E.p.r. spectra of [Cu(et2dtc)2], Na[Cu(asp/glut)(et2dtc)] and Na2[Cu(asp/glut)(et2dtc)2] in the polycrystalline state have
been recorded and discussed. The complexes display an antiferromagnetic exchange interaction, increasing in the order: Na2[Cu(asp/glut)(et2dtc)2]
< Na[Cu(asp/glut)(et2dtc)] < [Cu(et2dtc)2]
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
104.
105.
Summary Triisopropoxy bis(O,O-dialkyl dithiophosphates), (i-PrO)3M[S2P(OR)2]2 (M = Nbv, Tav; R = n-Pr, i-Pr, i-Bu and Ph) have been prepared by reacting the appropriate triisopropoxymetal(V)dichloride, (i-PrO)3MCl2 (1 mol) with sodium/ammonium dialkyl dithiophosphates (2 mols)in THF. The monomeric products which are viscous liquids, soluble in common organic solvents and highly susceptible to hydrolysis, were characterized by i.r. and n.m.r. spectra which indicate a bidentate mode of attachment of dithiophosphato groups to the metal. 相似文献
106.
Ghadwal Rajendra Singh Sharma Malti Singh Anirudh Mehrotra Ram C. 《Transition Metal Chemistry》2004,29(4):419-424
Complexes of the types VO(L)(R-deaH), VO(R-dea)(LH), and VO(L)(OGOH)[L = deprotonated form of N-(1-hydroxyethyl) naphthaldimine; R-dea = deprotonated form of a N-substituted diethanolamine, with R = H or Ph; G = CH2CH2, CHMeCHMe, CMe2CMe2, CHMeCH2CMe2, CMe2CH2CH2CMe2] have been prepared by the equimolar reactions of VO(OPr
i
)3, LH2, and an appropriate diethanolamine or glycol in benzene. All of these coloured solid complexes have been characterised by elemental (C, H, N, and V) analyses and by spectroscopic (i.r., electronic, 1H-, 51V-n.m.r) studies. The relative lability of the hydroxy group(s) of N-(1-hydroxyethyl)naphthaldiamine, diethanolamine, and glycol has also been investigated. 相似文献
107.
The reaction of the anticancer active compound [Rh(2)(mu-O(2)CCH(3))(2)(bpy)(2)(CH(3)CN)(2)][BF(4)](2) (1) (bpy = 2,2'-bipyridine) with NaC(6)H(5)S under anaerobic conditions yields Rh(2)(eta(1)-C(6)H(5)S)(2)(mu-C(6)H(5)S)(2)(bpy)(2).CH(3)OH (2), which was characterized by UV-visible, IR, and (1)H NMR spectroscopies as well as single-crystal X-ray crystallography. Compound 2 crystallizes as dark red platelets in the monoclinic space group C2/c with cell parameters a = 20.398(4) A, b = 11.861(2) A, c = 17.417(4) A, beta = 108.98 degrees, V = 3984.9(14) A(3), Z = 4. The main structural features are the presence of a [Rh(2)](4+) core with a Rh-Rh distance of 2.549(2) A bridged by two benzene thiolate ligands in a butterfly-type arrangement. The axial positions of the [Rh(2)](4+) core are occupied by two terminal benzene thiolates. Cyclic voltammetric studies of 2 reveal that the compound exhibits an irreversible oxidation at +0.046 V in CH(3)CN, which is in accord with the fact that the compound readily oxidizes in the presence of O(2). The fact that this unusual dirhodium(II/II) thiolate compound is formed under these conditions is an important first step in understanding the metabolism of dirhodium anticancer active compounds with thiol-containing peptides and proteins. 相似文献
108.
Alvarez-Puebla RA dos Santos DS Blanco C Echeverria JC Garrido JJ 《Journal of colloid and interface science》2005,285(1):41-49
Illite clays are known to have a strong affinity for metallic pollutants in the environment and can be applied as low-cost adsorbents for industrial waste treatment. A crucial factor in the development of such applications, however, is the understanding of the chemical, mineralogical, and colloidal properties of these clays. It is also important to understand the mechanisms involved in the surface adsorption of metals by these adsorbants. In order to study the retention of transition metals on illite clays, we have applied surface characterization techniques such as FPIA, SEM-EDX, XRD, N2 (77 K) adsorption, and FTIR. In addition to these experimental techniques, we have also employed a theoretical model that accounts for the chemistry of transition metal ions, and considers the global retention process to be the sum of several single retention processes. This model adequately fits the experimental data and allows for the speciation of metal retention on illite surfaces. Between pH values of 2.53 and 3.01 the only adsorption processes are the electrostatic sorption of [Cu(H2O)6]2+, and the surface complexation of [Cu(H2O)6]2+ and [Cu(OH)(H2O)5]+ ions. Surface complexation of [Cu(OH)(H2O)5]+ ions increases with pH, overcoming [Cu(H2O)6]2+ retention, and thus contributing to the surface precipitation of Cu(OH)2. 相似文献
109.
Bernabé-Pineda M Ramírez-Silva MT Tapia-Benavides R Rojas-Hernández A 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2004,60(5):1071-1076
The importance assigned to chelating agents in diverse areas has impelled studies concerning their development as related to metal ions representing a biological concern. The synthesis of di-isopropyliminodiacetoamide (D) is presented in this work. The acidity constant obtained for D was pKa = 5.79 +/- 0.04 with the aid of program SUPERQUAD. The equilibrium constants for D with Cu(II) were obtained with the aid of program SQUAD for CuD2+ and CuD2(2)+ species giving log beta1 = 4.795 +/- 0.002 and log beta2 = 8.374 +/- 0.004, respectively. 相似文献
110.