Cobalt complexes transition

Azo compounds o-am ino-o -hydroxy diary 1 transition metal complexes, 6,57 bidentate dyes, 6,42 o,o -diaminodiaryI cobalt complexes, 6,58,60 o,o -dihydroxydiaryl copper complexes. 6.55,57 pK 6,47... 

Polarographic studies are reported on thioesters, mainly of the type (140) and (141), and on trichloroethylphosphonites. In the field of nucleotides and nucleosides it is found that ATP has a very high surface activity at the mercury electrode, which is strongly dependent upon complex formation with transition metals. The polarographic behaviour of cobalt complexes with triphenylphosphine and its oxide has been studied in order to estimate extraction efficiencies. 

Coordination compounds have been produced by a variety of techniques for at least two centuries. Zeise s salt, K[Pt(C2H4)Cl3], dates from the early 1800s, and Werner s classic syntheses of cobalt complexes were described over a century ago. Synthetic techniques used to prepare coordination compounds range from simply mixing the reactants to employing nonaqueous solvent chemistry. In this section, a brief overview of some types of general synthetic procedures will be presented. In Chapter 21, a survey of the organometallic chemistry of transition metals will be presented, and additional preparative methods for complexes of that type will be described there. 

Modified cobalt complexes of the type frans-Co2(CO)6(phosphine)2 are promising candidates for certain transition metal-catalyzed reactions, in particular for the hydroformylation of long-chained olefins [117]. A series of complexes Co2(CO)6[P(alkyl) (aryl)m]2 (n 0,1,2,3 m S - n) was synthesized and used for solubility measurements. Since the basicity of phosphines affects the catalytic activity, use of fluorous substituents might induce unexpected changes in the activity. Therefore, also derivatives with an additional ethyl spacer between the fluorous group and the phosphine moiety were examined (Sect. 3.1). 

Rathke and Feder have employed Co2(CO)8 as the catalyst precursor in their studies. Samples withdrawn from reactions under pressure were analyzed for both total cobalt and for HCo(CO)4 (35) conversion to HCo(CO)4 was observed to the extent of 50-90%, varying according to (14) with temperature and hydrogen pressure. Experiments with different levels of catalyst showed that the overall rate of CO reduction was first-order in the HCo(CO)4 concentration, as determined by titration of reaction samples. Thus, there is substantial evidence that the catalyst in this system (or more precisely, the species present in the transition state of the rate-determining catalytic step) is a mononuclear cobalt complex. The observed kinetic dependences [Eq. 

In addition, a few other publications also address this issue of ballistic modification of composite propellants. The cobalt, nickel and zinc hexammine perchlorates have been studied by Gurdip Singh and coworkers for this purpose. The generated data indicate that cobalt complex accelerates burn rate three-fold when used at 2% level in HTPB-AP-based composite propellant [277]. Another study on transition metals (copper, iron, cobalt and nickel) salts of NTO as BRMs for HTPB-AP-based... 

The products isolated from reactions of amides with transition metal halides usually contain coordinated halide (e.g. the formulations in Table 2). In some cases such as [Co(NMF)6][CoCLt], halide and amide are coordinated to different metal atoms, but when such compounds are dissolved in the neat ligand, halide can be replaced and at high dilution all the metal ions may be fully coordinated by the amide alone. The electronic spectrum resulting when this cobalt complex is dissolved in nitromethane has been interpreted as relating solely to the tetrahedral complex [CoC12(NMF)2]. 

The metal-catalyzed oxidation of imines using molecular oxygen as the final oxidant and aldehydes as co-reductants has been studied223. Various transition metal complexes have been tested as catalysts and it is found that cobalt complexes can catalyze the selective oxidation of imines to oxaziridines in good yield (ca 80%) (Scheme 4). 

Nature demonstrates that transition metals can be very effective in catalyzing transformations, which are impossible to accomplish otherwise under physiological conditions. The prime example is vitamin B12, whose resting state is adenosylco-balamine(III) (reviews [267-273]). On homolysis it triggers a variety of radical reactions crucial to the living world. This inspired the interest of chemists and led to a number of applications. More recently, interest shifted to catalysis by low-valent cobalt complexes. 

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