Carboxylic acids iron complexes

Table 5. Carboxylic Acids 5 by Removal of the Chiral Auxiliary from Iron-Acyl Complexes 4...

Carboxylic acids, a-bromination of 55, 31 CARBOXYLIC ACID CHLORIDES, ketones from, 55, 122 CARBYLAMINE REACTION, 55, 96 Ceric ammonium nitrate [Ammonium hexa mtrocerate(IV)[, 55, 43 Chlorine, 55, 33, 35, 63 CHROMIUM TRIOXIDE-PYRIDINE COMPLEX, preparation in situ, 55, 84 Cinnamomtnle, a-phenyl- [2-Propeneni-tnle 2,3-diphenyl-], 55, 92 Copper(l) iodide, 55, 105, 123, 124 Copper thiophenoxide [Benzenethiol, copper(I) salt], 55, 123 CYCLIZATION, free radical, 55, 57 CYCLOBUTADIENE, 55, 43 Cyclobutadieneiron tricarbonyl [Iron, tn-carbonyl(r)4-l,3-cyclo-butadiene)-], 55,43... 

MnP is the most commonly widespread of the class II peroxidases [72, 73], It catalyzes a PLC -dependent oxidation of Mn2+ to Mn3+. The catalytic cycle is initiated by binding of H2O2 or an organic peroxide to the native ferric enzyme and formation of an iron-peroxide complex the Mn3+ ions finally produced after subsequent electron transfers are stabilized via chelation with organic acids like oxalate, malonate, malate, tartrate or lactate [74], The chelates of Mn3+ with carboxylic acids cause one-electron oxidation of various substrates thus, chelates and carboxylic acids can react with each other to form alkyl radicals, which after several reactions result in the production of other radicals. These final radicals are the source of autocataly tic ally produced peroxides and are used by MnP in the absence of H2O2. The versatile oxidative capacity of MnP is apparently due to the chelated Mn3+ ions, which act as diffusible redox-mediator and attacking, non-specifically, phenolic compounds such as biopolymers, milled wood, humic substances and several xenobiotics [72, 75, 76]. 

Nalidixic acid and sodium nalidixate form a strong colored complex with iron III. The maximum of absorbance of the complex is 410 nm and Beer s Law is obeyed from 10 to 250 yg of nalidixic acid per ml(33)5 and from 0.43 to 17.05 mg iron III per ml.(34) Nalidixic acid complexes through the oxo-group on C-4 and the carboxylic acid group on C-3. Three moles of nalidixic acid complex with one mole of iron III. The instability constant of the complex was calculated to be 2.11 x 10 8 by Dick and Murgu.(34)... 

Except for phthalic acid, all other carboxylic acids studied induce considerable increases in the light compared to the dark values (the relatively high rate of iron oxide dissolution induced by oxalic acid has been extensively studied (5,8). Phthalic acid actually appears to stabilize the iron oxide against photodissolution despite the solution phase complex exhibiting some photoactivity. 

Although not part of soil, lichens, by virtue of their solubilising action on rocks, contribute to the elemental enrichment of soil. Several studies have identified lichen acids as complexing agents for the iron and aluminium of rocks (95, 96). An examination of the various structures indicates that the basic structure responsible for the chelation is the carboxylic acid group with an orthophenolic group. Grodzinskii (97) has found lichens to be intense accumulators of elements in the uranium-radium, actinouranium and thorium orders. 

The use of carboxylic acids for the removal of iron(III) from solutions of the rare-earth metals has been reported,38 but has not been described in detail. The stoichiometries of the extracted complexes of iron(III) have not been clearly established. The n-decanoic acid complex has been variously described as (FeA3)3 and Fe3A9 x(OH) (HA) 51 or [Fe(OH)A2]2 and [Fe(OH)2A-HA]2,57 the H-octanoic acid complex as (FeA3-H20)3,58 the naphthenic acid complex as FeA3,47 and that of Versatic 10 acid as [FeA3(HA)J>, or [Fe(OH)A2]3.59... 

First, 1 2 metal complexes of (mainly mono-) azo dyes, without sulfonic or carboxylic acid groups, and trivalent metals (see Section 3.11). The metals are preferably chromium and cobalt nickel, manganese, iron, or aluminum are of lesser importance. Diazo components are mainly chloro- and nitroaminophenols or amino-phenol sulfonamides coupling components are (3-naphthol, resorcinol, and 1-phe-nyl-3-methyl-5-pyrazolone. Formation of a complex from an azo dye and a metal salt generally takes place in the presence of organic solvents, such as alcohols, pyridine, or formamide. An example is C.I. Solvent Red 8, 12715 [33270-70-1] (1). 

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