Synthesis, structure, and catalytic activity of binuclear lanthanide complexes with chiral NOBIN-based NNO ligands |
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Authors: | Qiuwen Wang Haibin Song |
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Affiliation: | a Department of Chemistry, Beijing Normal University, Beijing 100875, China b State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China |
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Abstract: | Two new amido binuclear complexes {(1)YN(SiMe3)2}2 · C7H8 (3 · C7H8) and {(2)SmN(SiMe3)2}2 · C6H14 (4 · C6H14) have been readily prepared in good yields by amine elimination reaction between Ln[N(SiMe3)2]3 (Ln = Sm, Y) and chiral NNO ligands, (S)-2-(pyridin-2-ylmethylamino)-2′-hydroxy-1,1′-binaphthyl (1H2) and (S)-5,5′,6,6′,7,7′,8,8′-octahydro-2-(pyrrol-2-ylmethyleneamino)-2′-hydroxy-1,1′-binaphthyl (2H2), respectively. They both have been characterized by various spectroscopic techniques, elemental analyses, and X-ray diffraction analyses. They are active catalysts for asymmetric hydroamination/cyclization of aminoalkenes and ring-opening polymerization of rac-lactide, affording cyclic amines in excellent conversions with moderate ee values and isotactic-rich polylactides, respectively. |
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Keywords: | 2-Amino-2&prime -hydroxy-1,1&prime -binaphthyl NNO ligands Chiral organolanthanide complexes Asymmetric hydroamination/cyclization Polymerization of lactide |
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