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Complexes of triamidoamines with the early actinides. Synthetic routes to monomeric compounds of tetravalent uranium and thorium containing halide and amide ligands

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UNSPECIFIED (1999) Complexes of triamidoamines with the early actinides. Synthetic routes to monomeric compounds of tetravalent uranium and thorium containing halide and amide ligands. INORGANIC CHEMISTRY, 38 (16). pp. 3651-3656. ISSN 0020-1669

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Abstract

The reaction of the lithiated triamidoamine [Li-3(NN'(3))(THF)(3)] [NN; = N(CH2CH2NSiMe2But)(3)] with AnCl(4) (An = U, Th) followed by sublimation gives monomeric [An(NN'3)Cl]. Reaction of these complexes with SiMe3X (X = Br, I) gives [An(NN'3)X]. The amido derivatives [An(NN'3)(NEt2)] are prepared from H-3(NN;) and [U(NEt2)(4)] and from [Th(NN;)CI] and [Li(NEt2)]. In each case, the complexes [U(NN;)X] (X = Cl, Br, I, NEt2) are shown by X-ray crystallography to contain a triamidoamine ligand disposed with 3-fold symmetry about the metal center. The structures are distorted from trigonal bipyramidal by displacement of the uranium atoms out of the equatorial plane of the three amido nitrogen atoms by ca. 0.8 Angstrom. The ligand backbone is distorted in such a manner as to cause the tert-butyldimethylsilyl groups to encircle the equatorial plane of the metal atom rather than surround the apical coordination site as is observed in the transition metal complexes of this type. Variation of the auxiliary ligand has little effect on the orientation, bond lengths, and angles within the (triamidoamine)uranium fragment. The tert-butydimethysilyl-substituted triamidoamine ligand is thus ideally suited for coordination to large metals since it stabilizes the formation of 3-fold symmetric structures while also allowing reactivity at the fifth coordination site.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: INORGANIC CHEMISTRY
Publisher: AMER CHEMICAL SOC
ISSN: 0020-1669
Date: 9 August 1999
Volume: 38
Number: 16
Number of Pages: 6
Page Range: pp. 3651-3656
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/14302

Data sourced from Thomson Reuters' Web of Knowledge

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