Mononuclear anionic formyl complexes; synthesis and properties

A series of kinetically unstable mononuclear anionic formyl complexes have been prepared by the action of Li(C₂H₅)₃BH on neutral metal carbonyl precursors. One of these, Li⁺[(CO)₄Mn(COC₆H₅)(CHO)]^?, is shown to decompose by a hydride transfer disproportionation mechanism involving the by-product (C₂H₅)₃B.     

Organic transformations via metal silane reagents: syntheses of vinyl ethers from dimethyl ketals and (CO)5MnSi(CH3)3

The reaction of dimethyl ketals with (CO)₅MnSi(CH₃)₃ ($\text{1}$ at 50 °C in CH₃CN affords methyl enol ethers, generally in 75–95% yields.     

Estimation of kinetic parameters in oxidative dehydrogenation of n-butenes over SnO2?Sb2O4 catalysts

Kinetic curves measured in the oxidation of n-butenes over a SnSb=31 mixed oxide catalyst were fitted by the kinetic model put forward in a previous paper. The goodness of fitting shows that the kinetic behavior of this complex reaction system can be described by a mechanism involving acidic and redox sites on the catalyst surface.

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- SnSb=31 , . , , - .