Wheaton Craig A, Hayes Paul G, Ireland Benjamin J
Department of Chemistry and Biochemistry, University of Lethbridge, Alberta, Canada.
Dalton Trans. 2009 Jul 7(25):4832-46. doi: 10.1039/b819107g. Epub 2009 Feb 17.
Interest in the utility of polylactide as a commodity polymer has increased significantly in recent years due to numerous environmental advantages over conventional petrochemically derived plastics. As such, the development of novel catalyst systems for the ring opening polymerization of lactide has seen tremendous progress in the past decade. In particular, divalent metals (i.e. Mg, Ca and Zn) supported by monoanionic ancillary scaffolds are appealing because of their low toxicity and cost. A much less common approach involves the use of neutral ligands in combination with the aforementioned divalent metal centres. The additional valence thus renders it possible, upon reaction with traditional Lewis or Brønsted acid activators, to generate sterically and electronically unsaturated species, akin to the most widely employed olefin polymerization catalysts. This Perspective is not intended as a comprehensive review, but rather a systematic highlight of key contributions, which have served to extend the forefront of this exciting field.
近年来,由于聚丙交酯相对于传统石油化学衍生塑料具有诸多环境优势,其作为商品聚合物的实用性受到了极大关注。因此,在过去十年中,用于丙交酯开环聚合的新型催化剂体系取得了巨大进展。特别是,由单阴离子辅助支架支撑的二价金属(即镁、钙和锌)因其低毒性和低成本而备受关注。一种不太常见的方法是将中性配体与上述二价金属中心结合使用。这样,与传统的路易斯或布朗斯特酸活化剂反应后,额外的化合价使得生成空间和电子不饱和的物种成为可能,这类似于应用最广泛的烯烃聚合催化剂。本展望并非全面综述,而是对关键贡献的系统重点介绍,这些贡献推动了这一令人兴奋的领域的前沿发展。