Applications iron/cobalt complexes

The most significant results obtained for complexes of iron(II) are collected in Table 3. The data derive from laser Raman temperature-jump measurements, ultrasonic relaxation, and the application of the photoperturbation technique. Where the results of two or three methods are available, a gratifying agreement is found. The rate constants span the narrow range between 4 x 10 and 2 X 10 s which shows that the spin-state interconversion process for iron(II) complexes is less rapid than for complexes of iron(III) and cobalt(II). 

The structures of metal-complex dyes, which must exhibit a high degree of stability during synthesis and application, is limited to certain elements in the first transition series, notably copper, chromium, iron, cobalt and nickel. The remaining members of the transition series form relatively unstable chelated complexes. The following description of the influence of electronic structure, however, is applicable to all members of the series. 

On the other hand, Tilley et al. have reported a synthesis of a well-defined tris(tert-butoxy)siloxy-iron(lll) complex [13] as well as respective molecular siloxide complexes of cobalt [14] and copper [15], which appear to become precursors for their grafting onto silica and application as catalysts for oxidation of alkanes, alkenes and arenes by hydrogen peroxide. 

Many transition-metal complexes have been widely studied in their application as catalysts in alkene epoxidation. Nickel is unique in the respect that its simple soluble salts such as Ni(N03)2 6H20 are completely ineffective in the catalytic epoxidation of alkenes, whereas soluble manganese, iron, cobalt, or copper salts in acetonitrile catalyze the epoxidation of stilbene or substituted alkenes with iodosylbenzene as oxidant. However, the Ni(II) complexes of tetraaza macrocycles as well as other chelating ligands dramatically enhance the reactivity of epoxidation of olefins (90, 91). 

Alatorre Ordaz, A., Manriquez Rocha, J., Acevedo Aguilar, F.J., Gutierrez Granados, S. and Bedioui, F. (2000) Electrocatalysis of the reduction of organic halide derivatives at modified electrodes coated by cobalt and iron macrocyclic complex-based films Application to the electrochemical determination of pollutants. Analusis 28, 238-244. 

Acid dyes include metal-complexed azo structures, where the metals used are cobalt, chromium, and iron.10 Examples are 1 1 and 2 3 chromium complexes and 1 2 cobalt complexes, where the numbers employed represent the ratio of metal atoms to dye molecules. Metal-complexed dyes can be formed inside textile fibers by treating suitably dyed fibers with a solution containing metal ions.11 In this case, the metal-free forms of these azo dyes are known as mordant dyes and contain mainly ortho, ortho -bis-hydroxy or ortho-carboxy, ortho -hydroxy groups (e.g., C.I. Mordant Black 11, Mordant Yellow 8, and Mordant Orange 6). When the metal complexes are formed prior to the dye application process, the resultant dyes are known as... 

Cobalt complexes among other metals such as iron and nickel are known to catalyze the growth of carbon nanotube (CNT) by chemical vapor deposition (CVD) [79-81]. Thanks to the thermal stability of the hyperbranched polyyne backbone, spin-coated films of the organometalhc polymer were successfully probed to function as catalyst and arrays of CNT bundles could be prepared (Figure 2.4). This preliminary result already suggests potential application in the field of paUemable tailor-made catalysts. 

The heptanuclear iron carbonyl cluster [Fe3(CO)u(/u-H)]2-Fe(DMF)4 (178) acted as an efficient catalyst in the reduction of carboxamides by l,2-bis(dimethylsilyl)benzene in toluene to the corresponding amines in high yields. Several tertiary and secondary amides including a sterically crowded amide were also reduced smoothly A review of the development of optically active cobalt complex catalysts for enan-tioselective synthetic reactions has addressed the applications of ketoiminatocobalt(II) complexes such as (5)-MPAC (179) and (5)-AMAC (180), transition-state models for borohydride reduction, halogen-free reduction by cobalt-carbene complexes. 

Catalytic reactions aimed at the formation of Csp -S and Csp -Se bonds are known to take place with rhodium, ruthenium and cobalt complexes. A particularly promising area with tremendous development in recent years concerns the investigation and possible application of iron catalysts. 

To commercialize LT-PE will require an understanding of how the kind of polyethylene and its microstructure affects its properties and applications. Interestingly, LT-PE can be divided into two types depending on whether the microstructure is linear or branched. Highly linear polyethylenes (including oligomers) are commonly produced by iron and cobalt complex pre-catalysts [22-31,41], whereas branched polyethylenes are formed by nickel and palladium complex pre-catalysts [17-21, 42], The microstmctural differences in LT-PE are caused by their characteristic mechanistic pathways of polymerization. 

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