Grafting of conductive polymers from poly(glycidyl methacrylate)-based macromolecular anchoring layer

PMSE 331

Nataliya Khanduyeva, Khanduyeva@ipfdd.de1, Vera Bocharova, bocharova@ipfdd.de1, Anton Kiriy, kiriy@ipfdd.de1, M. Stamm, stamm@ipfdd.de2, and Ulrich Oertel, oertel@ipfdd.de3. (1) Department of Nanostructured Materials, Leibniz Institute for Polymer Research Dresden, Hohe Strasse 6, 01069 Dresden, Germany, (2) Department of Nanostructured Materials, Leibniz Institut für Polymerforschung, Dresden e.V, Hohe Strasse 6, Dresden 01069, Germany, (3) Institute for Polymer Research, Department of Surface Modification, Leibniz Institute for Polymer Research Dresden, Hohe Strasse 6, Dresden, Germany
We report on the approach utilizing poly(glycidyl methacrylate)(PGMA) as a macromolecular anchor for growing of conductive polymers, for example, poly(3-hexyl thiophene)(PHT) on various surfaces: Si-wafer, glass, ITO-modified glass, and various metals (Al, Ti and Au). Our method relies on the deposition of thin strongly adherent PGMA films, followed by a modification with properly functionalised polymerizable compounds and, finally, chemical or electrochemical growing of CPs. This convenient method has the advantage of the modular approach, allowing easy tuning of head-groups thus optimising the polymerisation process and the properties of resulting CP brushes. PHT grafted to glass slides displays solvatochromism similarly to the dissolved PATs. This implies a certain conformational freedom of PHT chains despite the fact that they are tethered to the substrate.