End-functionalized diblock copolymers by mix and match of poly(2-oxazoline) and polyester building blocks

2-(4-(Iodomethyl)benzyl)isoindoline-1,3-dione was utilized as a protected amine-functionalized initiator for the cationic ring opening-polymerization (CROP) of 2-ethyl-2-oxazoline. As kinetic studies indicated a well-controlled polymerization, the CROP was terminated with sodium azide. Subsequent deprotection of the α-end group enabled successive attachment of a targeting ligand, e.g., retinoic acid or a proteogenic amino acid as a peptide model at the α-chain end. The heterotelechelic PEtOx were coupled to cyclooctyne end-functionalized polylactide, which was obtained by initiating the ring opening polymerization of l-lactide via a cyclooctyne based alcohol, utilizing strain-promoted azide-alkyne cycloaddidtion. In-depth characterization via mass spectrometry, 1H NMR spectroscopy, size exclusion chromatography, and infrared spectroscopy investigations verified the success of all synthetic steps and the preservation of retinoyl and leucine moieties also in the end-functionalized PEtOx-b-PLA block copolymers. Circumventing potential degradation of the polyester block during ligand attachment, the heterotelechelic PEtOx represents a universal building block useful for modular approaches towards tailored materials for nanomedicine.