| Literature DB >> 15740127 |
Harald Hofmeier1, Richard Hoogenboom, Marielle E L Wouters, Ulrich S Schubert.
Abstract
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.Entities:
Year: 2005 PMID: 15740127 DOI: 10.1021/ja042919e
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419