| Literature DB >> 31289694 |
Gabriela Gil Alvaradejo1,2,3, Hung V-T Nguyen3, Peter Harvey4,5,6, Nolan M Gallagher3, Dao Le1,2, M Francesca Ottaviani7, Alan Jasanoff4,5,6, Guillaume Delaittre1,2, Jeremiah A Johnson3.
Abstract
The synthesis of functional poly(2-alkyl-2-oxazoline) (PAOx) copolymers with complex nanoarchitectures using a graft-through ring-opening metathesis polymerization (ROMP) approach is described. First, well-defined norbornene-terminated poly(2-ethyl-2-oxazoline) (PEtOx) macromonomers (MM) were prepared by cationic ringopening polymerization. ROMP of these MMs produced bottlebrush copolymers with PEtOx side chains. In addition, PEtOx-based branched MMs bearing a terminal alkyne group were prepared and conjugated to an azide-containing bis-spirocyclohexyl nitroxide via Cu-catalyzed azide-alkyne cycloaddition (CuAAC). ROMP of this branched MM, followed by in situ cross-linking, provided PEtOx-based brush-arm star polymers (BASPs) with nitroxide radicals localized at the core-shell interface. These PEtOx-based nitroxide-containing BASPs displayed relaxivity values on par with state-of-the-art polyethylene glycol (PEG)-based nitroxide materials, making them promising as organic radical contrast agents for metal-free magnetic resonance imaging (MRI).Entities:
Year: 2019 PMID: 31289694 PMCID: PMC6615754 DOI: 10.1021/acsmacrolett.9b00016
Source DB: PubMed Journal: ACS Macro Lett Impact factor: 6.903