A healable supramolecular polymer blend based on aromatic π-π stacking and hydrogen bonding interactions

Full text not archived in this repository.

Please see our End User Agreement.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

Add to AnyAdd to TwitterAdd to FacebookAdd to LinkedinAdd to PinterestAdd to Email

Burattini, S., Greenland, B. W., Merino, D. H., Weng, W., Seppala, J., Colquhoun, H. M., Hayes, W. orcid id iconORCID: https://orcid.org/0000-0003-0047-2991, Mackay, M. E., Hamley, I. W. orcid id iconORCID: https://orcid.org/0000-0002-4549-0926 and Rowan, S. J. (2010) A healable supramolecular polymer blend based on aromatic π-π stacking and hydrogen bonding interactions. Journal of the American Chemical Society, 132 (34). pp. 12051-12058. ISSN 0002-7863 doi: 10.1021/ja104446r

Abstract/Summary

An elastomeric, supramolecular healable polymer blend, comprising a chain-folding polyimide and a telechelic polyurethane with pyrenyl endgroups, is compatibilised by aromatic π−π stacking between the π-electron-deficient diimide groups and the π-electron-rich pyrenyl units. This inter-polymer interaction is key to forming a tough, healable, elastomeric material. Variable temperature FTIR analysis of the bulk material also conclusively demonstrates the presence of hydrogen bonding, which complements the π–π stacking interactions. Variable temperature SAXS analysis shows that the healable polymeric blend has a nanophase-separated morphology, and that the X-ray contrast between the two types of domain increases with increasing temperature, a feature that is repeatable over several heating and cooling cycles. A fractured sample of this material reproducibly regains more than 95% of the tensile modulus, 91% of the elongation to break, and 77% of the modulus of toughness of the pristine material.

Altmetric Badge

Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/7382
Identification Number/DOI 10.1021/ja104446r
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Interdisciplinary centres and themes > Chemical Analysis Facility (CAF)
Publisher American Chemical Society
Download/View statistics View download statistics for this item

University Staff: Request a correction | Centaur Editors: Update this record

Search Google Scholar