Tu Yujie, Yu Yeqing, Xiao Diwen, Liu Junkai, Zhao Zheng, Liu Zhiyang, Lam Jacky W Y, Tang Ben Zhong
Department of Chemistry The Hong Kong University of Science and Technology Clear Water Bay, Kowloon Hong Kong China.
Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Institute for Advanced Study and HKUST-Shenzhen Research Institute The Hong Kong University of Science and Technology Clear Water Bay, Kowloon Hong Kong China.
Adv Sci (Weinh). 2020 Sep 6;7(20):2001845. doi: 10.1002/advs.202001845. eCollection 2020 Oct.
Intelligent stimulus-response (S/R) systems are the basis of natural process and machine control, which are intensively explored in biomimetic design and analytical/biological applications. However, nonmonotonic multi-S/R systems are still rarely studied so far. In this work, a rational design strategy is proposed to achieve such a unique S/R system by integrating opposite luminescence behaviors in one molecule. When solvent polarity increases, many heterocyclic or carbonyl-containing compounds often become more emissive due to the suppression of the proximity effect, whereas molecules with donor-acceptor (D-A) structures tend to be less emissive because of the twisted intramolecular charge transfer. Meanwhile, protonation on D/A moieties will weaken/strengthen the D-A interaction to result in blue/redshifted emissions. By combining a protonatable heterocyclic acceptor and a protonatable donor together in one molecule, nonmonotonic brightness responses to polarity stimuli and nonmonotonic color responses to pH stimuli can be achieved. The design strategy is successfully verified by a simple molecule named 4-(dimethylamino)styryl)quinoxalin-2(1)-one (ASQ). ASQ exhibits nonmonotonic responses to polarity and pH stimuli, and aggregation-induced emission (AIE) with a nonmonotonic AIE curve. Meanwhile, ASQ can be adjusted to emit white light in an acidic environment, and it shows multivalent functionalities including albumin protein sensing, ratiometric pH sensing, and amine gas sensing.
智能刺激-响应(S/R)系统是自然过程和机器控制的基础,在仿生设计以及分析/生物应用中得到了深入研究。然而,非单调多S/R系统迄今为止仍很少被研究。在这项工作中,提出了一种合理的设计策略,通过在一个分子中整合相反的发光行为来实现这种独特的S/R系统。当溶剂极性增加时,许多含杂环或羰基的化合物由于邻近效应的抑制往往会变得更具发射性,而具有供体-受体(D-A)结构的分子由于分子内扭转电荷转移往往发射性降低。同时,D/A部分的质子化将减弱/增强D-A相互作用,导致发射蓝移/红移。通过在一个分子中结合一个可质子化的杂环受体和一个可质子化的供体,可以实现对极性刺激的非单调亮度响应和对pH刺激的非单调颜色响应。该设计策略通过一个名为4-(二甲基氨基)苯乙烯基喹喔啉-2(1)-酮(ASQ)的简单分子成功得到验证。ASQ对极性和pH刺激表现出非单调响应,以及具有非单调聚集诱导发光(AIE)曲线的AIE。同时,ASQ可以被调节在酸性环境中发射白光,并且它显示出包括白蛋白蛋白质传感、比率pH传感和胺气传感在内的多价功能。