Iron complexes catalytic chain transfer

Other complexes also react with propagating radicals by catalytic chain transfer." These include certain chromium,molybdenumand iron complexes. To date the complexes described appear substantially less active than the cobaloximes and are more prone to side reactions. 

The process implies a first electrochemical step with a very fast conversion of the ferroceno/ferrocinium couple, due to the short length of the alkyl chain, and a second chemical step with a simple electron transfer between the iron complex in solution and that of the monolayer. Moreover, the thiols block the gold surface in such a way that the Fe(CN)g- oxidation will take place due solely to the ferrocene mediation at the monolayer, and with a very high efficiency (i.e., the catalytic way is observed at potentials 500 mV lower than those corresponding to a gold electrode with a C6SH monolayer). 

The formation of the monocationic intermediate (ArH)2Fe+ attendant upon the charge-transfer excitation of either the ferrocene or methylan-thracene EDA complex (7a and 7b) is responsible for the photo-induced de-ligation of bis(arene)iron(II), as described in (6). Thus, transient electrochemical studies (Karpinski and Kochi, 1992a,b) show that the catalytic de-ligation of (ArH)2Fe+ proceeds rapidly via a (two-step) electron-transfer chain or ETC process (8). 

Hiatt et a/.34a-d studied the decomposition of solutions of tert-butyl hydroperoxide in chlorobenzene at 25°C in the presence of catalytic amounts of cobalt, iron, cerium, vanadium, and lead complexes. The time required for complete decomposition of the hydroperoxide varied from a few minutes for cobalt carboxylates to several days for lead naphthenate. The products consisted of approximately 86% tert-butyl alcohol, 12% di-fe/T-butyl peroxide, and 93% oxygen, and were independent of the catalysts. A radical-induced chain decomposition of the usual type,135 initiated by a redox decomposition of the hydroperoxide, was postulated to explain these results. When reactions were carried out in alkane solvents (RH), shorter kinetic chain lengths and lower yields of oxygen and di-te/T-butyl peroxide were observed due to competing hydrogen transfer of rm-butoxy radicals with the solvent. 

Transition-metal/sulfide sites, especially those containing iron, are present in all forms of life and are found at the active centers of a wide variety of redox and catalytic proteins. These proteins include simple soluble electron-transfer agents (the ferredoxins), membrane-bound components of electron-transfer chains, and some of the most complex metalloenzymes, such as nitrogenase, hydrogenase, and xanthine oxidase. 

This process is integrated within the respiratory electron-transport chain involved in the mitochondria of cells. Yeast CCP is easy to purify and has been widely studied. The complex between CCP and cytochrome c was crystallized in 1992. The electron-transfer pathway involves primarily Trp-191 and then Gly-192, Ala-193, and Ala-194. When Trp-191 is replaced by phenylalanine, the rate of the catalytic reaction is reduced by a factor of 1,000. Unlike other Cpd I formulations, CCP Cpd I consists of an iron(IV)-oxo and a radical-cation on Trp-191. 

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