کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1325533 | 1499940 | 2010 | 6 صفحه PDF | دانلود رایگان |
A series of organolanthanide complexes supported by a new ferrocene-containing N-aryloxo-functionalized β-ketoiminate ligand FcCOCH2C(Me)N(2-HO-5-Me-C6H3) (LH2, Fc = ferrocenyl) was synthesized by amine elimination reactions. It was found that the ionic radii have a profound effect on the outcome of the reactions. Reactions of LH2 with Ln[N(SiMe3)2]3(μ-Cl)Li(THF)3 in a 1:1 molar ratio in THF gave the desired lanthanide amido complexes [LLn{N(SiMe3)2}(THF)]2 [Ln = Nd (1), Sm (2), Er (3), Yb (4), Y (5)] in good isolated yields, whereas the similar reaction of LH2 with La[N(SiMe3)2]3(μ-Cl)Li(THF)3 gave he unexpected lanthanum–lithium heterobimetallic cluster [L2La{μ-Li(THF)}2(μ-Cl)]2 (6). These complexes were characterized by IR spectroscopy, elemental analysis, and 1H NMR spectroscopy in the case of complexes 5 and 6. The definitive molecular structures of complexes 1, 2, 4 and 6 were determined by X-ray diffraction studies. Complexes 1–5 can initiate the ring-opening polymerization of l-lactide with moderate activity.
A series of organolanthanide complexes supported by a new ferrocene-containing N-aryloxo-functionalized β-ketoiminate ligand was synthesized by amine elimination reactions, and it was found that the ionic radii have a profound effect on the outcome of the reactions.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 695, Issues 25–26, 1–15 December 2010, Pages 2726–2731