IDEAS home Printed from https://ideas.repec.org/a/gam/jsusta/v1y2009i4p1226-1239d6462.html
   My bibliography  Save this article

New Challenge for Classics: Neutral Zinc Complexes Stabilised by 2,2’-Bipyridine and 1,10-Phenanthroline and Their Application in the Ring-Opening Polymerisation of Lactide

Author

Listed:
  • Janna Börner

    (Department Chemie, Universität Paderborn, Warburger Straße 100, 33098 Paderborn, Germany)

  • Ulrich Flörke

    (Department Chemie, Universität Paderborn, Warburger Straße 100, 33098 Paderborn, Germany)

  • Artjom Döring

    (Department Chemie, Universität Paderborn, Warburger Straße 100, 33098 Paderborn, Germany)

  • Dirk Kuckling

    (Department Chemie, Universität Paderborn, Warburger Straße 100, 33098 Paderborn, Germany)

  • Matthew D. Jones

    (Department of Chemistry, University of Bath, Claverton Down, Bath BA27AY, UK)

  • Sonja Herres-Pawlis

    (Department Chemie, Technische Universität Dortmund, Otto-Hahn-Straße 6, 44227 Dortmund, Germany)

Abstract

The zinc acetato and triflato complexes of 2,2’-bipyridine and 1,10-phenanthroline were prepared and completely characterised. The whole series (including the already described dichlorido complexes and the ligands themselves) were screened for their catalytic activity in the solvent free ring-opening polymerisation of D,L-lactide. The acetato and triflato complexes were found to be active initiators and polylactides could be obtained in almost quantitative yields or with high molecular weights, up to 145,000 g/mol.

Suggested Citation

  • Janna Börner & Ulrich Flörke & Artjom Döring & Dirk Kuckling & Matthew D. Jones & Sonja Herres-Pawlis, 2009. "New Challenge for Classics: Neutral Zinc Complexes Stabilised by 2,2’-Bipyridine and 1,10-Phenanthroline and Their Application in the Ring-Opening Polymerisation of Lactide," Sustainability, MDPI, vol. 1(4), pages 1-14, December.
  • Handle: RePEc:gam:jsusta:v:1:y:2009:i:4:p:1226-1239:d:6462
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/2071-1050/1/4/1226/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/2071-1050/1/4/1226/
    Download Restriction: no
    ---><---

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jsusta:v:1:y:2009:i:4:p:1226-1239:d:6462. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.