Niu Jia, Page Zachariah A, Dolinski Neil D, Anastasaki Athina, Hsueh Andy T, Soh H Tom, Hawker Craig J
Department of Chemistry, Boston College, Chestnut Hill, Massachusetts 02467, United States.
ACS Macro Lett. 2017 Oct 17;6(10):1109-1113. doi: 10.1021/acsmacrolett.7b00587. Epub 2017 Sep 22.
We report a simple procedure for rapid, visible light-mediated, controlled radical polymerization in aqueous solutions. Based on the photoelectron transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization, fast chain propagation at room temperature in water was achieved in the presence of reductant and without prior deoxygenation. A systematic study correlating irradiation intensity and polymerization kinetics, enabled by in situ nuclear magnetic resonance spectroscopy, provided optimized reaction conditions. The versatility of this procedure was demonstrated through a rapid triblock copolymer synthesis, and incorporation of water-labile activated esters for direct conjugation of hydrophilic small molecules and proteins. In addition, this technique boasts excellent temporal control and provides a wide range of macromolecular materials with controlled molecular weights and narrow molecular weight distributions.
我们报道了一种在水溶液中进行快速、可见光介导的可控自由基聚合的简单方法。基于光电子转移可逆加成-断裂链转移(PET-RAFT)聚合,在有还原剂存在且无需预先脱氧的情况下,实现了在室温下于水中的快速链增长。通过原位核磁共振光谱对辐照强度与聚合动力学进行的系统研究,提供了优化的反应条件。通过快速合成三嵌段共聚物以及引入对水不稳定的活性酯以实现亲水性小分子和蛋白质的直接共轭,证明了该方法的通用性。此外,该技术具有出色的时间控制能力,可提供多种具有可控分子量和窄分子量分布的高分子材料。