The synthesis and ring-opening metathesis polymerization of an amphiphilicredox-active norbornene

The synthesis and characterization of an amphiphilic, ferrocenyl-modified n orbornene is reported. Linked together through a quaternary ammonium salt, the norbornenyl moiety makes this monomer susceptible to ring-opening metat hesis polymerization (ROMP) using (PCy3)(2)RuCl2=CHPh, while the ferrocenyl group allows for the incorporation of a redox-active group in the polymer backbone. The resulting polymers are soluble in both aqueous and organic me dia. Such polymers are important for the development of materials for elect rochemically-based diagnostic applications. Cyclic voltammetry studies reve aled that reversible redox waves are observed for both the monomer and poly mer, although the E-1/2 of the polymer is approximately 145 mV lower than t hat of the monomer, reflecting very different local environments. (C) 2000 Elsevier Science S.A. All rights reserved.