Estupiñán Diego, Gegenhuber Thomas, Blinco James P, Barner-Kowollik Christopher, Barner Leonie
Institut für Biologische Grenzflächen, Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany.
Preparative Macromolecular Chemistry, Institut für Technische Chemie und Polymerchemie, Karlsruhe Institute of Technology (KIT), Engesserstr. 18, 76131 Karlsruhe, Germany.
ACS Macro Lett. 2017 Mar 21;6(3):229-234. doi: 10.1021/acsmacrolett.7b00024. Epub 2017 Feb 17.
We introduce an inherently fluorescent self-reporting step-growth polymer system as well as a fluorescence-based methodology for accessing the kinetics of the underpinning photoinduced nitrile imine-mediated tetrazole-ene cycloaddition (NITEC) process, using an equimolar mixture of a bismaleimide linker and a bifunctional α,ω-tetrazole-chain transfer agent (CTA). Similarly, α,ω-tetrazole-capped polystyrene, prepared via RAFT polymerization, was employed as a photoreactive macromonomer. Upon UV irradiation, the tetrazole moiety readily reacts with activated dialkenes producing the fluorescent pyrazoline-containing polymer. Thus, the fluorescence emission of the step-growth polymers is directly correlated with the number of ligation points in the polymer, forming an ideal self-reporting sensor system. The viability of the fluorescence-based quantification is verified via NMR spectroscopy, evidencing that fluorescence-based polymerization monitoring is a viable avenue in cases where NMR spectroscopy is difficult to conduct.
我们介绍了一种具有固有荧光的自报告逐步增长聚合物体系,以及一种基于荧光的方法,用于研究光诱导腈亚胺介导的四唑-烯环加成反应(NITEC)的动力学,该方法使用双马来酰亚胺连接体和双官能α,ω-四唑链转移剂(CTA)的等摩尔混合物。同样,通过可逆加成-断裂链转移(RAFT)聚合制备的α,ω-四唑封端的聚苯乙烯被用作光反应性大分子单体。在紫外线照射下,四唑部分很容易与活化的二烯烃反应,生成含荧光吡唑啉的聚合物。因此,逐步增长聚合物的荧光发射与聚合物中的连接点数直接相关,形成了一个理想的自报告传感器系统。基于荧光的定量分析的可行性通过核磁共振光谱得到验证,这表明在难以进行核磁共振光谱分析的情况下,基于荧光的聚合监测是一种可行的途径。