摘要:
The reaction of (Me3Si)(i-Pr2P)NH with ZnEt2 gives the complex {[(Me3Si)(i-Pr2P)N]ZnEt}(2), which was characterized by multinuclear NMR spectroscopy and X-ray crystallography. This Zn complex reacts with CO2 to give an adduct with the proposed formula of [(Me3Si)N(i-Pr2PCO2)]ZnEt that undergoes further transformation into the crystallographically characterized di-adduct [(Me3Si)N(i-Pr2PCO2)](2)Zn, in addition to a Zn-6 cluster containing both P-CO2 adducts and fragments of the isocyanate i-Pr2P-N=C=O. These reaction pathways have been separately observed in related group 2 and group 14 complexes, but not previously within the same molecule. Reactions with the related heteroallene CS2 were also examined. The free ligand (Me3Si)(i-Pr2P)NH reacts with CS2 to form a bright red, crystalline adduct (Me-3 Si)[P(i-Pr)(2)(CS2)]NH. This adduct was treated with ZnEt2 to provide the same product that is obtained from the reaction of {[(Me3Si)(i-Pr2P)N]ZnEt}(2) with CS2, proposed to be a dithiocarbamate complex, with the CS2 bound to the N instead of the P atom. (C) 2012 Elsevier Ltd. All rights reserved.