Light-driven folding of single polymer chains via metal-complexation†
Abstract
We introduce a light-driven methodology (λmax = 365 nm) to fold single polymer chains into single chain nanoparticles (SCNPs). Exploiting the photo-isomerization of spiropyran entities embedded into the backbone of polymer chains (ranging from 15 to 38 mol%) constituted of polyethylene glycol carrying monomer units (ranging from Mn = 28 500 g mol−1 to 40 000 g mol−1), we complex their open form using a range of metals, including iron, copper and cobalt. The approach offers the first direct avenue for incorporating metals into SCNPs via a photochemical folding mechanism in one step.
- This article is part of the themed collection: Polymer Chemistry 15th Anniversary Collection