Oxygen coordination complex catalysts

Earlandite structure, 849 Electrical conductivity metal complexes, 133 tetracyanoplatinates anion-deficient salts, 136 Electrical properties metal complexes, 133-154 Electrocatalysis, 28 Electrochemical cells, 1 Electrochemistry, 1-33 hydrogen or oxygen production from water coordination complex catalysts, 532 mineral processing, 831 reduction, 831 Electrodeposi (ion of metals, 1-15 mineral processing difficulty, 831 Electrodes clay modified, 23 ferrocene modified, 20 nation coated, 15 polymers on, 16 polyvinylferrocene coated, 19 poly(4-vinylpyridine) coated, 17 redox centres, 17 Prussian blue modified, 21 surface modified, 15-31 Electrolysis... 

The divalent Co(salen) complex (69a) is one of the most versatile and well-studied Co coordination compounds. It has a long and well-documented history and we shall not restate this here. Recent applications of (69a) as both a synthetic oxygen carrier and as a catalyst for organic transformations are described in Sections 6.1.3.1.2 and 6.1.4.1 respectively. Isotropic shifts in the HNMR spectrum of low-spin Co(salphn) (69b) were investigated in deuterated chloroform, DMF, DMSO, and pyridine.319 Solvent-dependent isotropic shifts indicate that the single unpaired electron, delocalized over the tetradentate 7r-electron system in CHCI3, is an intrinsic property of the planar four-coordinate complex. The high-spin/low-spin equilibrium of the... 

This stabilization may also be interpreted in terms of oxygen anions, which, due, to the vacancy, are initially double bonded to Mo. One electron is transferred to the catalyst in this reaction step. To form acrolein, a second hydrogen atom is transferred (to form water) and an oxygen atom is bonded to the allyl radical. In this (rather complex) process, another three electrons are transferred to the catalysts and doubtless distributed over several Mo ions. Reoxidation takes place at the bismuth cations, where oxygen molecules are attracted by the free electron pair. The intermediate result is a surface bismuth with an oxygen coordination similar to that in the bulk, viz. 

Some nickel(II) tetraaza macrocycles have been proved to act as efficient catalysts for the electrochemical reduction of C02 in H20/MeCN medium. This indirect electroreduction occurs at potentials in the range -1.3 to -1.6 V vs. SCE and mainly produces either CO or a CO/H2 mixture, depending upon the type of complex.2854 The five-coordinate complexes [NiL] (394) formed by some deprotonated dioxopentamine macrocycles have been found to display very low oxidation potentials Nin/Nira in aqueous solution (about 0.24-0.25 V vs. SCE at 25 °C and 0.5 M Na2S04). Air oxidation of the same complexes in aqueous solution yields 1 1 NiL-02 adducts (5 = 1) which are better formulated as superoxo complexes, NimL-02 (Scheme 56). The activation of Ni-bound oxygen is such that it attacks benzene to give phenol.2855... 

COORDINATION COMPLEXES AS CATALYSTS FOR THE ELECTROCHEMICAL PRODUCTION OF HYDROGEN OR OXYGEN FROM WATER... 

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