Strasser Paul, Plavcan Oliver, Ajvazi Edip, Henke Helena, Brüggemann Oliver, Teasdale Ian
Institute of Polymer Chemistry Johannes Kepler University Linz Linz Austria.
Centre for Additive Manufacturing University of Nottingham, Jubilee Campus, Wollaton Road Nottingham, NG8 1BB UK.
J Polym Sci (2020). 2022 Jul 1;60(13):2000-2007. doi: 10.1002/pol.20220066. Epub 2022 Apr 8.
The control of chain-ends is fundamental in modern macromolecular chemistry for directed one-to-one bioconjugation and the synthesis of advanced architectures such as block copolymers or bottlebrush polymers and the preparation of advanced soft materials. Polyphosphazenes are of growing importance as elastomers, biodegradable materials and in biomedical drug delivery due to their synthetic versatility. While controlled polymerization methods have been known for some time, controlling both chain-ends with high fidelity has proven difficult. We demonstrate a robust synthetic route to hetero and homo α,ω-chain-end functionalized polyphosphazenes via end-capping with easily accessible, functionalized triphenylphosphine-based phosphoranimines. A versatile thiol-ene "click"-reaction approach then allows for subsequent conversion of the end-capped polymers with various functional groups. Finally, we demonstrate the utility of this system to prepare gels based on homo α,ω-chain-end functionalized polyphosphazenes. This development will enhance their progress in various applications, particularly in soft materials and as degradable polymers.
在现代高分子化学中,链端控制对于定向一对一生物共轭、合成先进结构(如嵌段共聚物或刷状聚合物)以及制备先进软材料至关重要。聚磷腈由于其合成的多功能性,作为弹性体、生物可降解材料以及在生物医学药物递送方面的重要性日益增加。虽然可控聚合方法已为人所知一段时间,但要以高保真度控制两个链端已证明很困难。我们展示了一种通过用易于获得的、功能化的三苯基膦基磷亚胺进行封端,来合成杂化和均相α,ω链端功能化聚磷腈的稳健合成路线。一种通用的硫醇-烯“点击”反应方法随后允许用各种功能基团对封端聚合物进行后续转化。最后,我们展示了该系统用于制备基于均相α,ω链端功能化聚磷腈的凝胶的实用性。这一进展将促进它们在各种应用中的发展,特别是在软材料和作为可降解聚合物方面的应用。