Tsuchiya Tomoaki, Mizuno Hiroaki, Fukuhara Gaku
Department of Chemistry, Tokyo Institute of Technology 2-12-1 Ookayama Meguro-ku Tokyo 152-8551 Japan
JST, PRESTO 4-1-8 Honcho Kawaguchi Saitama 332-0012 Japan.
RSC Adv. 2021 Sep 14;11(48):30472-30478. doi: 10.1039/d1ra05795b. eCollection 2021 Sep 6.
The newly designed polythiophene chemosensors (PT1 and PT2) were synthesized the Suzuki-Miyaura polymerization with appropriate yields. The photophysical properties of PTs thus obtained were examined by means of UV/vis, fluorescence, excitation spectroscopy, and time-correlated single-photon-counting method. The π-π* transitions around 400-600 nm and the emissions in the range of 400-650 nm were observed. The binding behavior of PTs was also investigated upon the interaction of tetrabutylammonium or tetrabutylphosphonium isophthalate, affording the binding constants () of 5790-8310 M, which were quite smaller than those observed in the corresponding repeating unit. The comprehensive analyses of the UV/vis data and theoretical calculation supports revealed the origins of scope and limitation toward signal-amplification sensing. The present results obtained herein will guide the development of new amplification chemosensors.
通过铃木-宫浦聚合反应以适当产率合成了新设计的聚噻吩化学传感器(PT1和PT2)。通过紫外可见光谱、荧光光谱、激发光谱和时间相关单光子计数法对由此获得的聚噻吩的光物理性质进行了研究。观察到在400-600nm附近的π-π*跃迁以及在400-650nm范围内的发射。还研究了聚噻吩与间苯二甲酸四丁铵或四丁基鏻相互作用时的结合行为,得到的结合常数()为5790-8310 M,这比在相应重复单元中观察到的结合常数小得多。对紫外可见光谱数据的综合分析和理论计算支持揭示了信号放大传感的范围和局限性的根源。本文获得的当前结果将指导新型放大化学传感器的开发。