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Ring-opening polymerization of lactides catalyzed by magnesium complexes coordinated with NNO-tridentate pyrazolonate ligands

Authors

  • Hui-Ju Chuang,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Hsiao-Li Chen,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Jian-Li Ye,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Zn-Yun Chen,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Pei-Ling Huang,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Tzu-Ting Liao,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Tsung-En Tsai,

    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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  • Chu-Chieh Lin

    Corresponding author
    1. Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
    • Department of Chemistry and Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan, Republic of China
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Abstract

A series of magnesium benzylalkoxide complexes, [LnMg(μ-OBn)]2 (114) supported by NNO-tridentate pyrazolonate ligands with various electron withdrawing-donating subsituents have been synthesized and characterized. X-ray crystal structural studies revealed that Complexes 13, 5, 7, 9, and 10 are dinuclear bridging through benzylalkoxy oxygen atoms with penta-coordinated metal centers. All of these complexes acted as efficient initiators for the ring-opening polymerization of L-lactide and rac-lactide. Based on kinetic studies, the activity of these metal complexes is significantly influenced by the electronic effect of the ancillary ligands with the electron-donating substituents at the phenyl rings enhancing the polymerization rate. In addition, the “living” and “immortal” character of 6 has paved a way to synthesize as much as 40-fold polymer chains of polylactides with a very narrow polydispersity index in the presence of a small amount of initiator. Among all of magnesium complexes, Complex 6 exhibits the highest stereoselectivity toward ring-opening polymerization of rac-lactide with Pr up to 88% in THF at 0 °C. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

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