Beryllium Dichloride Coordination by Nitrogen Donor Molecules

Abstract

Abstract The reaction of anhydrous beryllium chloride with nitrogen donors L in diethylether as a solvent under mild conditions affords 1:2 complexes of the type L2BeCl2 [L = benzonitrile (1), pyridine (2), 3,5-dimethylpyridine, pyrrolidine, piperidine (8), and diethylamine (10)]. Structural studies of compounds 1, 2, 8 (CHCl3), and 10 have shown that the complexes have the beryllium centers N2Cl2- tetracoordinated with a distorted tetrahedral geometry of the core unit. In crystals of 8 and 10 these molecules are associated to form helical strings via distinct N-H-Cl hydrogen bonding. The reaction of the weak donor pyrazole (pyz) with (Et2O)2BeCl2 at low temperature gives the mixed complex [(Et2O)(pyz)BeCl2] (4), in which one diethylether molecule is retained in the inner coordination sphere of the metal. In tetrahydrofuran (thf) solution, no reaction is observed with pyrazole, indicating that tetrahydrofuran is the stronger donor as compared to pyrazole, and the (thf)2BeCl2 solvate remains intact. By contrast, with the strong base pyrrolidine (pyrr) the same reaction leads to substitution of one chloride ligand to give the ionic product [(pyrr)3BeCl]+Cl−, (7). Both products (4, 7) have been structurally characterized. At room temperature the reactions with pyrazole or piperidine lead to ether cleavage as a side-reaction which may even become dominant at long reaction times and more forcing conditions. Dinuclear complexes of the type [LBeCl(μ2-OR)]2 are formed, the structures of which have also been determined. The results suggest that hydrogen bonding may assist in the ether cleavage process, since this reaction is not observed for ligands devoid of N-H functions.