Chlorite anion

However, at pH values closer to neutrality (i.e. at the mean salivary pH of 5.97), chlorite anion itself can effect the oxidative decarboxylation of pyruvate to acetate and CO2 (Equation 1.12). 

Immobilized TEMPO has been used for the one-pot oxidation of alcohols to carboxylic acids as well.26 For this purpose TEMPO resin 1 was combined with two ion-exchange resins loaded with chlorite anions and hydrogen phosphate in the presence of catalytic amounts of potassium bromide and sodium hypochlorite in solution. The reaction required work-up for the removal of salts, but tolerated several protecting schemes and afforded pure products in good to excellent yields. The reaction is initiated by catalytic TEMPO oxidation of alcohols to aldehydes driven by dissolved hypochlorite followed by oxidation to the carboxylic acids effected by chlorite. 

Oxidation of oxalic acid with dimethyl-V,V-dichlorohydantoin and dichloroisocya-nuric acid is of first order with respect to the oxidant. The order with respect to the reductant is fractional. The reactions are catalysed by Mn(II). Suitable mechanisms are proposed.129 A mechanism involving synchronous oxidative decarboxylation has been suggested for the oxidation of a-amino acids with l,3-dichloro-5,5-dimethylhydantoin.130 Kinetic parameters have been determined and a mechanism has been proposed for the oxidation of thiadiazole and oxadiazole with trichloroiso-cyanuric acid.131 Oxidation of two phenoxazine dyes, Nile Blue and Meldola Blue, with acidic chlorite and hypochlorous acid is of first order with respect to each of the reductant and chlorite anion. The rate constants and activation parameters for the oxidation have been determined.132... 

For anions that end in -ite, the suffix of the acid is -ous. For example, the acid of the chlorite anion, CIO2", is chlorous acid, HCIO2. 

Aquation of the chlorito complex [Co(NH3)5(C102)] forms part of the overall substitution and redox reactivity pattern established for this complex. Indeed the mechanism of aquation involves an internal redox process. Rate constants and activation parameters for aquation of this chlorito complex in acidic aqueous solution are k29 = 8.0 x 10 s A// = 105 kJ mol and AS = + 13 J mol Although this complex could hardly be described as robust, the chlorite anion is considerably less fragile when coordinated to cobalt(III) than when bonded to Cobalt(III)-amine complexes of organic carbox-... 

The oxo-anions of chlorine are weaker oxidants than the corresponding acids. Because they are also more stable, it is not too difficult to isolate certain salts of those acids that can be obtained only in aqueous solution. Hypochlorites and chlorites are hydroly2ed in aqueous solution since HOCl and HCIO2 have acid dissociation constants of 10 and 10 , respectively however, aqueous chloric and perchloric acids are hiUy iorrhed. 

Hypochlorites, chlorites, chlorates and perchlorates all represent the same dangers, which are linked to the fact that they are strong oxidants. The danger is not directly linked to the importance of the oxidation state of chlorine atom and this is partly for kinetic reasons. The main factors of the accidents described in the technical literature are not the intrinsic properties of each anion, but rather the frequency with which they are used. So chlorates and perchlorates are more often involved in accidents than hypochlorites and especially chlorites, which are hardly used. Thus the classification below does not provide positive indications about the dangerous properties of each substance mention. ... 

Figure 10 Capillary ion analysis of 30 anions 1 = thiosulfate, 2 = bromide, 3 = chloride, 4 = sulfate, 5 = nitrite, 6 = nitrate, 7 = molybdate, 8 = azide, 9 = tungstate, 10 = monofluorophosphate, 11 = chlorate, 12 = citrate, 13 = fluoride, 14 = formate, 15 = phosphate, 16 = phosphite, 17 = chlorite, 18 = galactarate, 19 = carbonate, 20 = acetate, 21 = ethanesulphonate, 22 = propionate, 23 = propanesulphonate, 24 = butyrate, 25 = butanesulphonate, 26 = valerate, 27 = benzoate, 28 = D-glutamate, 29 = pentane-sulphonate and 30 = D-gluconate. Experimental conditions fused silica capillary, 60 cm (Ld 52 cm) x 50 p i.d., voltage 30 kV, indirect UV detection at 254 nm, 5 mM chromate, 0.5 mM NICE-Pak OFM Anion-BT, adjusted to pH 8.0, with 100 mM NaOH. (From Jones, W. R. and Jandik, R, /. Chromatogr., 546, 445,1991. With permission.)...

Arts, (a) Sodium chlorite and (b) barium hypochlorite. Note that parentheses enclose the CIO" ions, because there is a subscript to show that there are two of them. In (a), there is only one anion, which contains two oxygen atoms. 

The adsorption of transition metal complexes by minerals is often followed by reactions which change the coordination environment around the metal ion. Thus in the adsorption of hexaamminechromium(III) and tris(ethylenediamine) chromium(III) by chlorite, illite and kaolinite, XPS showed that hydrolysis reactions occurred, leading to the formation of aqua complexes (67). In a similar manner, dehydration of hexaaraminecobalt(III) and chloropentaamminecobalt(III) adsorbed on montmorillonite led to the formation of cobalt(II) hydroxide and ammonium ions (68), the reaction being conveniently followed by the IR absorbance of the ammonium ions. Demetallation of complexes can also occur, as in the case of dehydration of tin tetra(4-pyridyl) porphyrin adsorbed on Na hectorite (69). The reaction, which was observed using UV-visible and luminescence spectroscopy, was reversible indicating that the Sn(IV) cation and porphyrin anion remained close to one another after destruction of the complex. 

This class covers the four levels of oxidation represented in the series hypochlorite, chlorite, chlorate and perchlorate, and as expected, the oxidising power of the anion is roughly proportional to the oxygen content, though stability factors are also important. The class has been subdivided under the group headings below, each of which has its own listing of member compounds. 

A few DBFs, such as bromate, chlorate, iodate, and chlorite, are present as anions in drinking water. As a result, they are not volatile and cannot be analyzed by GC/MS. They are also difficult to separate by LC, but will separate nicely using ion chromatography (IC). At neutral pH, HAAs are also anions and can be separated using 1C. A number of methods have been created for these DBFs using both IC/ inductively coupled plasma (ICF)-MS and IC/ESl-MS. Fretreatment to remove interfering ions (e.g., sulfate and chloride), along with the use of a suppressor column prior to introduction into the MS interface, is beneficial for trace-level measurement. 

Because chlorite is an anion, sorption of chlorite ions onto suspend particles, sediment, or clay surfaces is expected to be limited under enviromnental conditions. Thus, chlorite ions may be mobile in soils and leach into groundwater. However, chlorite (ions or salts) will undergo oxidation-reduction reactions with components in soils, suspend particles, and sediments (e.g., Fe, Mn ions see Section 6.3.2.2). Thus, oxidation-reduction reactions may reduce the concentration of chlorite ions capable of leaching into groundwater. 

A< Ba(Q02)2.Bcirium is an alkaline ecirth metal (Group IIA) and thus has a chcii e of -1-2. You should recognize chlorite as the name of a polyatomic ion. In fact, any anion name that doesn t end in -ide should scream polyatomic ion to you. As Table 6-1 shows, chlorite is ClOj , which reveals that the chlorite ion has a-1 charge. Two chlorite ions cire necessary to neutralize the -1-2 chcirge of a single barium cation, so the chemical formula is Ba(C102)2-... 

Cellulosic Fibers. Substantivity for cellulosic fibers is offered mainly by anionic FWAs, preferably with sulfonic acid groups. Brighteners such as 14,19, 24, and 26 with moderate to high affinities are suitable for batch processes. If simultaneous bleaching takes place in the same bath, the brightener must be stable with respect to bleaching chemicals such as peroxide or chlorite [126],... 

The kinetics of the oxidation of l-phenyl-2-thiourea by chlorite, in aqueous acidic media, are strongly influenced by the pH and show a complex acid dependence. The proposed mechanism involves HOC1 as a major intermediate whose autocatalytic production determines the observed kinetics of the reaction. The oxidation involved the formation of two stable intermediates, the sulfinic acid and the sulfonic acid, on the pathway towards total desulfurization to form phenylurea. A comprehensive 29-reaction scheme has been proposed to describe the observed complex kinetics.96 The oxidation of trimethylthiourea (TMTU) by chlorite in slightly acidic media is very fast. The oxidation of TMTU proceeds through the formation of sulfinic acid then to the sulfoxylate anion. The direct reaction of chlorine dioxide and TMTU is autocatalytic and is also inhibited by acid. A series of 28 reactions have been proposed to describe the mechanism.97... 

International Standard Organization. 1997. Water quality. Determination of dissolved anions by liquid chromatography of ions. Part 4 Determination of chlorate, chloride and chlorite in water with low contamination. ISO 10304-4. International Organization for Standardization, Case Postale 56, CH-1211, Geneva 20 Switzerland. 

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