Synthesis of Trinuclear, Dinuclear and Mononuclear Carbamato‐Zinc Complexes from Tetranuclear Precursors: A Top‐Down Synthetic Approach to New Carbamates

Abstract

Abstract In this work we report on the synthesis of new mono‐, bi‐ and trinuclear carbamato‐Zn complexes by reaction of the tetranuclear precursor [ZnEt(O 2 CNR 2 )] 4 (R = i Pr and i Bu) with the nitrogen bases pyridine, N , N , N ′, N ′‐tetramethylguanidine (tmg) and bis( N , N , N′ , N′ ‐tetramethylguanidino)naphthalene (btmgn). The only reaction product obtained with pyridine is the dinuclear complex [(py)ZnEt(O 2 CNR 2 )] 2 . In the case of reaction of [ZnEt(O 2 CNR 2 )] 4 with tmg, the dinuclear species [(tmg)ZnEt(O 2 CNR 2 )] 2 (for molar ratios of 1:4) and the mononuclear bis‐carbamato complex [(tmg) 2 Zn(O 2 CNR 2 ) 2 ] (for molar ratios of 1:8) were obtained. Finally, the mono‐ and trinuclear carbamates [(btmgn)ZnEt(O 2 CNR 2 )] and [(btmgn)Zn 3 Et 3 (O 2 CNR 2 ) 3 ] were formed in the reaction between [ZnEt(O 2 CNR 2 )] 4 and btmgn (molar ratios 1:4 and 1:2, respectively). All products were structurally characterized by X‐ray diffraction. Using this top‐down approach the synthesis of a variety of oligonuclear carbamato‐Zn complexes becomes possible. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)