Role of hydrophobic interactions in the self-assembly of alternating copolymers

POSTER

Abstract

New nanomaterials already play a key role in several emerging technologies. Among the methods used to fabricate new nanomaterials, the most successful in producing precise structure is the bottom-up method. The materials obtained by self-assembly are ordered on different scales and respond and adapt to the presence of other molecules in their environment [1] and can therefore be used as probes, sensors or switches [2]. In this paper, we will describes the self-assembly of amphiphilic alternating copolymers into nanoarchitectures in aqueous solution. To investigate the role of the nature of the hydrophobic groups on the association, the self-assembly of two polymers are compared: poly(isobutylene-alt-maleic anhydride) (IMA) and poly(styrene-alt-maleic anhydride) (SMA) [3, 4]. The theoretical prediction is also compared to experiment and the characterization using Small Angle Neutron Scattering, Dynamic Light Scattering and High Resolution Transmission Electron Microscopy will be presented in detail. [1] S. Zhang, \textit{Nature Biotechnology}, 21, 10, 1171, 2003. [2] F. Patolsky, \textit{et al.}, \textit{Nanomedicine}, 1, 51-65, 2006 [3] C. Malardier-Jugroot, \textit{et al.,} \textit{J. of Phys. Chem. B}, 109(15), 7022-7032, 2005 [4] A.S.W. Chan, \textit{et al.}, \textit{Mol. Sim.}, accepted for publication, 2009.

*We gratefully acknowledge the support of NSERC(Canada), DGLEPM and Academic Research Program - RMC funding.

Authors

  • Cecile Malardier-Jugroot

    • Royal Military College of Canada
  • Anita S.W. Chan

    • Royal Military College of Canada
  • Michael N. Groves

    • Royal Military College of Canada