1. Synthesis and structural characterisation of divalent transition metal complexes containing an unsymmetrical benzamidinate ligand
- Author
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Chi-Keung Lam, Hung-Wing Li, Tung Suet Lam, Sze Man Fung, and Hung Kay Lee
- Subjects
chemistry.chemical_classification ,Denticity ,Stereochemistry ,Ligand ,General Chemistry ,Medicinal chemistry ,Catalysis ,Divalent ,Metal ,chemistry.chemical_compound ,Transition metal ,chemistry ,visual_art ,Materials Chemistry ,visual_art.visual_art_medium ,Chelation ,Stoichiometry ,Derivative (chemistry) - Abstract
The unsymmetrical benzamidinate ligand [PhC(NSiMe3)(NAr)]− (Ar = 2,6-Me2C6H3), denoted L−, and its lithium derivative [LiL(TMEDA)] (1) (TMEDA = N,N,N′,N′-tetramethylethylenediamine) have been prepared. Treatment of 1 with MCl2 (M = Mn, Co, Fe or Ni) afforded the corresponding divalent transition metal benzamidinates with interesting molecular structures. The reaction of two equivalents of 1 with MnCl2 or CoCl2 afforded the centrosymmetric binuclear complexes [(ML2)2·(TMEDA)] (M = Mn 2, Co 5). On the other hand, the reaction of FeCl2 with 1, in an appropriate stoichiometric ratio, led to the mononuclear mono(benzamidinate) [FeL(Cl)(TMEDA)] (3) and the bis(benzamidinate) [FeL2(TMEDA)] (4) complexes. The addition of two equivalents of 1 to NiCl2 yielded the mononuclear [NiL2] (6). X-Ray crystallography revealed that the κ2-benzamidinate ligand L− is bonded to the metal centre of these complexes in an unsymmetrical fashion. The TMEDA ligand in 2–5 exhibits different coordination modes. It acts as a chelating ligand in 3, as a monodentate ligand in 4, and as an unusual N,N′-bridging ligand in 2 and 5.
- Published
- 2003
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