| Literature DB >> 29965750 |
Hendrik Frisch1, Jan P Menzel1, Fabian R Bloesser1, David E Marschner1,2, Kai Mundsinger1, Christopher Barner-Kowollik1,2.
Abstract
Emulating nature's protein paradigm, single-chain nanoparticles (SCNP) are an emerging class of nanomaterials. Synthetic access to SCNPs is limited by ultralow concentrations, demanding reaction conditions, and complex isolation procedures after single-chain collapse. Herein, we exploit the visible light photodimerization of styrylpyrene units as chain folding mechanism. Critically, their positioning along the polymer chain creates a confined environment, increasing the photocycloaddition quantum yields dramatically, enabling single-chain folding at unrivaled high concentrations without subsequent purification. Importantly, the enhanced photoreactivity allows for single-chain folding at λ = 445 nm LED-irradiation within minutes as well as via ambient light, enabling an unprecedented folding system. The herein demonstrated enhancement of quantum yields by steric confinement serves as a blueprint for all photochemical ligation systems.Entities:
Year: 2018 PMID: 29965750 DOI: 10.1021/jacs.8b04531
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419