Iodination oxidizing agents used

Iodine is a weak oxidizing agent used primarily for the determination of strong reductants. The most accurate description of the half-reaction for iodine in these applications is... 

Because of their use in the rubber industry various sulfenamido thiazoles (131) have been prepared. They are obtained in good yields through the oxidation of A-4-thiazoline-2-thiones (130) in aqueous alkaline solution in the presence of an amine or ammonia (Scheme 66) <123, 166, 255, 286, 308, 309). Other oxidizing agents have been proposed (54, 148. 310-313) such as iodine (152), chlorine, or hydrogen peroxide. Disulfides can also be used as starting materials (3141. 

Complete iodination of organic compounds can be achieved by preventing the formation of free hydrogen iodide through the addition of an oxidizing agent, neutralization of the HI with a base, or combination using mercuric salts. 

Oxaziridines are powerful oxidizing agents. Free halogen is formed from hydrobromic acid (B-67MI50800). Reduction by iodide in acidic media generally yields a carbonyl compound, an amine and two equivalents of iodine from an oxaziridine (1). With 2-alkyl-, 2-acyl and with N-unsubstituted oxaziridines the reaction proceeds practically quantitatively and has been used in characterization. Owing to fast competing reactions, iodide reduction of 2-aryloxaziridines does not proceed quantitatively but may serve as a hint to their presence. 

Of the four halogens, iodine is the weakest oxidizing agent. Tincture of iodine, a 10% solution of I2 in alcohol, is sometimes used as an antiseptic. Hospitals most often use a product called povidone-iodine, a quite powerful iodine-containing antiseptic and disinfectant, which can be diluted with water to the desired strength. These applications of molecular iodine should not delude you into thinking that the solid is harmless. On the contrary, if I2(s) is allowed to remain in contact with your skin, it can cause painful bums that are slow to heal. 

L.19 Iodine is a common oxidizing agent, often used as the triiodide ion, I3. Suppose that in the presence of HCI(aq),... 

The resultant radical (86) can, in turn, be reduced back to the carbanion by shaking with sodium amalgam. In suitable cases, e.g. (87), the oxidation of carbanions with one-electron oxidising agents, usually iodine, can be useful synthetically for forming a carbon-carbon bond, through dimerisation (— 88) of the resultant radical (89) ... 

Due to the limited extent of this paper, we mention only some positive results achieved in the orientation to two main directions i.e. to oxidative principles and to alcoholates in aprotic solvents. The research of oxidative principles (see e.g. [9]), involved the use of compounds with active chlorine, active iodine, peroxo-compounds, various mixtures of these compounds, as well as the use of oxidative agents with enhancing solubility and thus decontamination efficiency by adding detergents. It can... 

Iodometry is an indirect procedure based on the aforesaid reversible reaction whereby the assay of oxidizing agents, for instance available chlorine in bleaching powder, cupric and ferric salts may be carried out by reducing them with an excess potassium iodide thereby liberating an equivalent quantity of iodine which can be estimated using a standard solution of thiosulphate. 

As it has been discussed earlier, iodine cannot be used directly as an oxidizing agent in such type of assays, whereas the liberated iodine quantitatively produced by the oxidation of iodide with bromine (excess) may be assayed by titrating against sodium thiosulphate solution. 

Potassium iodate is a fairly strong oxidizing agent that may be used in the assay of a number of pharmaceutical substances, for instance benzalkonium chloride, cetrimide, hydralazine hydrochloride, potassium iodide, phenylhydrazine hydrochloride, semicarbazide hydrochloride and the like. Under appropriate experimental parameters the iodate reacts quantitatively with both iodides and iodine. It is, however, interesting to observe here that the iodate titrations may be carried out effectively in the presence of saturated organic acids, alcohol and a host of other organic substances. 

Electrophilic substitution of 3-methoxy-4-methylaniline (655) by the complex 663 leads to the molybdenum complex 664. Oxidative cyclization of complex 664 with concomitant aromatization using activated commercial manganese dioxide provides 2-methoxy-3-methylcarbazole (37) in 53% yield (560). In contrast, cyclization of the corresponding tricarbonyliron complex to 37 was achieved in a maximum yield of 11 % on a small scale using iodine in pyridine as the oxidizing agent (see Scheme 5.49). 

Iodine pentoxide is used for analysis of carbon monoxide and for CO removal from air. It also is used as an oxidizing agent in other oxidation reactions. 

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