Photo-liberated amines for -carboxyanhydride (PLANCA) ring-opening polymerization

• Published in: Polymer chemistry 2021-07, Vol.12 (28), p.414-411
• Main Authors: Goodrich, Sofia L, Hill, Megan R, Olson, Rebecca A, Sumerlin, Brent S
• Format: Article
• ISSN: 1759-9954; 1759-9962
• DOI: 10.1039/d1py00781e

The polymerization of N -carboxyanhydrides (NCAs) affords access to a vast array of synthetic polypeptides with tunable molecular weights, functionalities, and architectures. The use of light to achieve spatiotemporal control over these polymerizations could expand their applicability to a variety of areas, including 3D printing and photolithography. In this report we utilized 2-(2-nitrophenyl)propyloxycarbonyl (NPPOC) as a photoprotecting group to cage a primary amine initiator that is activated upon UV irradiation. NPPOC photocages underwent quantitative deprotection and afforded better polymerization control compared to previously reported photocaged amines for NCA polymerizations. Furthermore, the addition of a small equivalence of base enhanced the control and resulted in polymers with lower dispersities. Overall, this method advances photo-controlled polypeptide synthesis by demonstrating high chain-end fidelity, efficient chain extension, and the ability to synthesize block copolymers. Photo-liberated amines for N- carboxyanhydride (PLANCA) ring-opening polymerization affords narrow molecular weights, chain-end retention, and the formation of block copolypeptides.