Oxo-chalcogenates

By contrast to the metaphosphimates, the metaphosphate analogues in which two chalcogens are replaced by imido groups form dimeric, dianionic ligands (24). There is only one example of a metal complex of the oxo system (24, E = O). An N,0-chelated bis(dimethylalumimun) complex is prepared by the reaction of two equivalents of trimethylaliuninum with ds-[ BuNH(0)P(//-N Bu)2P-(0)NH Bu] [20]. The structure of this complex is comparable to that of (15). 

In contrast to the chalcogen-bridged complexes, no similar oxygen-bridged compounds of iron, cobalt, or nickel exist. However, we obtained such oxo or i-ol-carbonyl complexes of chromium and its homologs, as well as of rhenium. The compounds are the products of the reactions of the respective metal carbonyls with bases (VII). 

The ligands that have been used in the preparation of metal nitride complexes are quite varied. They include halides, carbogenic groups (alkyl moiety and Cp ), pnic-togens (amine, amide, imide, phosphine, and arsine), and chalcogens (ether, alkox-ide, oxo, thioalkoxide, and selenides). Chart 1 provides a listing of the various ligands and the associated nitrido metal complexes. 

Further reactions of P-hydridocyclotriphosphazenes (See Section IV,E) have been described. They undergo insertion reactions with aldehydes, ketones, isothiocyanates and electrophilic olefins. Addition of sulfur or oxidation with KMn04 gives thioxo-or oxo-cyclotriphos-phazene derivatives which are methylated at the chalcogen to afford methylthio- and methoxy- cyclotriphosphazenes (36). Hydridocyclo-phosphazenes can also be oxidized to give symmetric and unsymmetric bis(cyclotriphosphazenyl) oxides (35). 

Both monomeric oxo- and thioxosilanes, X2Si=0 and X2Si=S, respectively, contain silicon in a trigonal-planar coordination. Their strongly polarized silicon-chalcogen double bonds, Si =0 and Si =S , render them kinetically unstable unless efficient protecting substituents X are present at silicon. The first kinetically stabilized thioxosilane, stable at ambient temperature, has recently been described. Stable oxosilanes have, however, not been isolated to date, and their synthesis continues to challenge experimentalists. ... 

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