Hofmeier Harald, Hoogenboom Richard, Wouters Marielle E L, Schubert Ulrich S
Laboratory of Macromolecular Chemistry and Nanoscience, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
J Am Chem Soc. 2005 Mar 9;127(9):2913-21. doi: 10.1021/ja042919e.
Using a hydroxy-functionalized terpyridine as initiator, a poly(epsilon-caprolactone) containing one terpyridine endgroup was prepared by tin octanoate-catalyzed controlled ring-opening polymerization. The omega-hydroxy group of this polymer was subsequently reacted with an isocyanato-ureidopyrimidinone, resulting for the first time in polymers bearing a metal-coordinating ligand on the one and a hydrogen-bonding unit on the other chain end. Hydrogen-bonded supramolecular dimers were shown to be present in chloroform solution. The subsequent addition of iron(II) ions resulted in the formation of high molecular weight supramolecular polymers with novel properties resulting from the combination of both types of noncovalent interactions in the main chain, as could be shown using capillary viscosimetry and rheometry.
以羟基官能化的三联吡啶为引发剂,通过辛酸亚锡催化的可控开环聚合反应制备了含一个三联吡啶端基的聚(ε-己内酯)。该聚合物的ω-羟基随后与异氰酸酯基脲嘧啶酮反应,首次得到了一条链端带有金属配位配体而另一端带有氢键单元的聚合物。在氯仿溶液中显示存在氢键超分子二聚体。随后加入亚铁离子导致形成了具有新型性质的高分子量超分子聚合物,这是由主链中两种非共价相互作用的结合所致,这一点通过毛细管粘度测定法和流变学得以证实。