Wu Chenyu, Chen Hengqi, Corrigan Nathaniel, Jung Kenward, Kan Xiaonan, Li Zhibo, Liu Wenjian, Xu Jiangtao, Boyer Cyrille
Key Laboratory of Biobased Polymer Materials, Shandong Provincial Education Department, School of Polymer Science and Engineering , Qingdao University of Science and Technology , Qingdao 266042 , China.
Qingdao Institute for Theoretical and Computational Sciences , Shandong University , Qingdao 266237 , China.
J Am Chem Soc. 2019 May 22;141(20):8207-8220. doi: 10.1021/jacs.9b01096. Epub 2019 May 7.
In this work, we adopted a fully computer-guided strategy in discovering an efficient pH-switchable organic photocatalyst (OPC), unprecedentedly turning colorless at pH 5 and recovering strong visible-light absorption and photoactivity at pH 7. This is the first example of an OPC design fully guided by comprehensive density functional theory (DFT) studies covering electrostatic, electrochemical, and photophysical predictions. Characterization of the designed OPC after synthesis confirmed the computational predictions. We applied this OPC to mediate an aqueous photoinduced electron/energy transfer-reversible addition-fragmentation chain transfer (PET-RAFT) polymerization under green LED light (nominal emission wavelength: 530 nm, 5 mW/cm). We demonstrated that the polymerization can be reversibly ceased by a slight change of pH (pH ≤ 5.0) or in the absence of light. Furthermore, we demonstrated that the polymerization rate could be significantly retarded by bubbling carbon dioxide into the reaction solution under visible light. Conversely, the rate could be fully recovered via exposure to nitrogen gas. This is the first example of a pH and light dual-gated polymerization system with complete and reversible inhibition.
在这项工作中,我们采用了一种完全由计算机引导的策略来发现一种高效的pH可切换有机光催化剂(OPC),该催化剂在pH 5时前所未有的变为无色,并在pH 7时恢复强烈的可见光吸收和光活性。这是首个完全由涵盖静电、电化学和光物理预测的综合密度泛函理论(DFT)研究引导的OPC设计实例。合成后对所设计的OPC进行表征证实了计算预测结果。我们将这种OPC应用于在绿色LED光(标称发射波长:530 nm,5 mW/cm)下介导水相光诱导电子/能量转移-可逆加成-断裂链转移(PET-RAFT)聚合反应。我们证明,通过略微改变pH(pH≤5.0)或在无光条件下,聚合反应可以可逆地停止。此外,我们证明,在可见光下向反应溶液中通入二氧化碳可显著减缓聚合速率。相反,通过暴露于氮气中,速率可以完全恢复。这是首个具有完全可逆抑制作用的pH和光双门控聚合体系实例。