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Complexation by metals

The general, selective and specific formation of complexes by metallic cations. G. Schwarzenbaeh, Adv. Inorg. Chem. Radiochem., 1961, 3, 257-285 (70). [Pg.29]

The equation for the formation of a complex by metal A and ligand B is written as... [Pg.671]

The photophysical properties (extinction coefficient, shifts in absorption and emission spectra, quantum yield, and lifetime) of a variety of probes are modified by pH changes, complexation by metal ions, or redox reactions. The resulting changes in photophysical parameters can be used to determine concentration of H+ and metal cations with suitably designed fluorophores. Most of these resulting sensors involve an equilibrium between the analyte, A, and the free probe (unprotonated or noncom-plexed by metal ion), Pf. If the stoichiometry of this reaction is 1 1, the reaction may be represented by... [Pg.307]

The General, Selective, and Specific Formation of Complexes by Metallic Cations... [Pg.407]

Reductive lithiation of allyl phenyl sulfides.1 This reagent is particularly useful for preparation of allyllithium reagents at temperatures at which the anions are stable. Moreover, regioselectivity in reactions can be achieved by conversion to allyltitanium(IV) complexes by metal exchange with Ti(0-/-Pr)4. Thus the un-symmetrical anion formed from the allyl sulfide 1 with LDMAN reacts with cro-tonaldehyde to give a mixture of 1,2- and 1,4-adducts. The 1,2-adduct 2 can be obtained in high yield as two diastereomers (9 1) by use of the allyltitanium complex (equation I). [Pg.165]

Complexation by metal oxides and clays. The adsorption processes of metals on silica, alumina, hydrated ferric oxide and a range of other minerals are well documented for laboratory studies performed with synthetic materials (Buffle, 1988 Dzombak and Morel, 1990 Stumm, 1992). The approaches described for major sites are applicable in this case. Nevertheless, the relevance of these data to natural water... [Pg.208]

Catalytic constants for iodination of 2-acetylpyridine (HS) complexed by metal ions"- ... [Pg.20]

This square planar zinc complex is an excellent intermediate for the preparation of other BZO4 [16] octaene N4 complexes by metal exchange, and its use alleviates the problem of separating the desired complex from other reaction side products when o-aminobenzaldehyde is condensed in the presence of the appropriate metal ion. Complexes of nickel, cobalt, iron, and palladium have been prepared from this zinc compound. [Pg.34]

Spectroscopic Characterization of Inorganic and Organometallic Complexes by Metal and High-Pressure NMR... [Pg.204]

It is difficult to estimate what the rate of the metal ion catalyzed oxidative deamination reaction of amino acids would be in natural waters. Hamilton and Revesz (30) found that the rate of oxidation of alanine in the presence of pyridoxal and manganese ions was inhibited by EDTA. Since metal ions in natural waters can be complexed by a variety of organic and inorganic compounds, their effectiveness in catalyzing the oxidative deamination of amino acids may be reduced. Also, the fraction of dissolved amino acids which would be complexed by metal ions at the pH and metal ion and amino acid concentrations found in natural waters must be considered. At neutral pH, where the amino group of the amino acid is protonated, the fraction of the amino acid that would be in the form of the metal ion complex depends upon the equilibrium constant for the formation of the complex and the pK of the amino proton of the amino acid. The reactions for the formation of the Cu2+-alanine complexes can be written as... [Pg.321]

Reactivity of Various Tertiary Diamines in the Preparation of Tertiary Diamine Organolithium Complexes by Metalation. Previous work has shown that the reactivity and the rate of metalation for Reaction 2 of the tertiary diamine organolithium complexes is a function of the tertiary diamine in the complex (1,9). In the specific case of the metala-... [Pg.32]

S.8.2.4.6. tt-Allyl Metal Complexes by Metal-Atom and Related Reactions. [Pg.167]


See other pages where Complexation by metals is mentioned: [Pg.436]    [Pg.376]    [Pg.432]    [Pg.188]    [Pg.194]    [Pg.158]    [Pg.375]    [Pg.379]    [Pg.297]    [Pg.4918]    [Pg.384]    [Pg.259]    [Pg.167]    [Pg.452]    [Pg.4917]    [Pg.214]    [Pg.367]    [Pg.232]    [Pg.390]   
See also in sourсe #XX -- [ Pg.292 ]




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Activation of C-H bonds by metal complexes

Activation of Dioxygen by Cobalt Group Metal Complexes

Activation of Silicon Bonds by Transition Metal Salts and Complexes

Alkene isomerizations catalyzed by transition metal complexes

Aromatic Substitution by Metal Catalysis or Other Complex Mechanisms

Aryl-Metal Complexes by Electrophilic Attack on Arenes

Aryl-Metal Complexes by Oxidative Addition of Arenes

By metal ions and complexes

Carbon dioxide activation by metal complexes

Catalysis by Metal Complexes and Chiral Phosphoric Acids

Catalysis by Water-Soluble Polymer-Metal Complexes

Catalysis by metal complexes

DNA and RNA Cleavage by Metal Complexes

Dioxygen activation by transition metal complexes

Energy transfer quenching by metal complexes

Functionalization of Arenes via C—H Bond Activation Catalysed by Transition Metal Complexes Synergy between Experiment and Theory

Group 7 metal-promoted oxidations epoxidation by salen manganese complexes

Homogeneous Catalysis by Transition Metal Complexes

Hydrocarbon Activation by Transition-Metal Complexes

Hydrogenation Reactions Catalyzed by Transition Metal Complexes

Inhibition by metal complexes

Metal impurities by complexation

N-Arene complexes by metal atom reactions

Other reactions catalyzed by transition-metal complexes

Oxidation Reactions Catalyzed by NHC-Coordinated Metal Complexes

Oxidation of Organic Substrates by Metal Ion Complexes

Oxidation of transition metal complexes by hydroxyl radicals

Photo-and Peroxide-Initiated Catalysis by Metal Complexes

Polymerization by Transition Metal Complexes

Promoted by transition metal complexes

Quinone Methide Stabilization by Metal Complexation

Reactions Catalyzed by Transition Metal Complexes

Rearrangements by Metal Ions and Complexes

Redistribution Reactions on Silicon Catalyzed by Transition Metal Complexes

Redistributions Catalyzed by Transition Metal Complexes

Reduction by complex metal hydride

Reduction of transition metal complexes by organic radicals

Relevance to cross-coupling reactions catalyzed by transition metal complexes

Stabilization of unstable d-metal oxidation states by complex formation

Synthesis of solvento-complexes by metal oxidation in non-aqueous solvents

The General, Selective, and Specific Formation of Complexes by Metallic

Vinyl-Metal Complexes by

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