Journal of the Chemical Society Dalton Transactions · 2000 · 47 citations · 18 references
Natural SciencesChemistryMaterials ScienceCrystal StructureInorganic ChemistryOrganic ChemistryCoordination ChemistryCrystal ChemistryLanthanide ChemistryMetal-ligand BondingTransition Metal ComplexesX-ray CrystallographyAmine FunctionalizationCrystalline StructureLanthanide ComplexesLanthanide Coordination ChemistryLanthanide HalidesLanthanide Nitrogen Donor LigandsLanthanide Organometallic ChemistryLithium Intercalation Compounds
Lithium, aluminium, gallium, lanthanum and cerium complexes of the new amidinato ligand −N(SiMe3)C(Ph)N(CH2)3NMe2 (≡L−), having a γ-pendant amine functionality, have been prepared. The dimeric lithium amidinate 1 was obtained in four steps from 1-amino-3-(dimethylamino)propane. Using 1 and MCl3 in appropriate stoichiometry led to the mononuclear M(L)Cl2 (M = Al 2 or Ga 3) and the dinuclear [{M(L)2(μ-Cl)}2] (M = La 4 or Ce 5). Structures of four of these (1, 2, 3 and 5) have been studied by X-ray crystallography. In crystalline 1 each amidinato ligand L− is chelating with respect to one of the lithium atoms and bridging by virtue of its pendant γ-tertiary nitrogen atom to the second Li atom. In 2 and 3, by contrast, L− behaves as a tripodal chelating ligand, whereas in crystalline 5 the seven-co-ordinate Ce atom is bound by two bidentate benzamidinato fragments and only one of the pendant amines.
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