Nitrogen-containing complexes transition metal

Pt-based catalysts are two necessary approaches at the current technology stage. It is believed that non-noble metal electrocatalysts is probably the sustainable solution for PEM fuel cell commercialization. In the past several decades, various nonnoble metal catalysts for ORR have been explored, including non-pyrolyzed and pyrolyzed transition metal nitrogen-containing complexes, transition metal chalcogenides, conductive polymer-based catalysts, metal oxides/carbides/nitrides/ oxynitrides/carbonitrides, and enzymatic compoimds. The major effort in non-noble metal electrocatalysts for ORR is to increase both the catalytic activity and stability. 

Besides the ferrocene crown ether ligands described earlier, a variety of related macrocyclic ferrocenophanes containing various sulfur, oxygen, and nitrogen heteroatoms have been reported by a number of groups (110-115) (Scheme 21). These ligands complex transition metal guest cations such as Ag(I), Cu(I), and Pd(II) (116,117). Of particular... 

Metal complexes of ligands containing a sulfur donor in conjunction with nitrogen, oxygen or a second sulfur have been reviewed in the past [11-13]. For example, reviews of the coordination compounds of dithiophosphates [14], dithiocarbamates [15, 16], dithiolates [17], dithiodiketonates [18], and xanthates [16] have appeared. The analytical aspects [19] and the spectral and structural information of transition metal complexes of thiosemicarbazones [20, 21] have been reviewed previously. Recent developments in the structural nature of metal complexes of 2-heterocyclic thiosemicarbazones and S-alkyldithiocarbazates, depicted below, are correlated to their biological activities. 

Whereas most of the known silylamines containing both a silicon halogen and nitrogen hydrogen unit undergo rapid condensation with HC1 elimination [11], transition metal substitution of the silicon provides unexpected high thermal stability. Compounds of this type are available via reaction of the dichlorosilyl complexes 18a-c with bulky primary amines to generate 19a-c (Eq. (4)). 

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