Ho Feng-Cheng, Huang Yi-Jing, Weng Chang-Ching, Wu Chia-Hua, Li Yaw-Kuen, Wu Judy I, Lin Hong-Cheu
Department of Materials Science and Engineering, National Chiao Tung University, Hsinchu 300, Taiwan.
Department of Applied Chemistry, National Chiao Tung University, Hsinchu 300, Taiwan.
ACS Appl Mater Interfaces. 2020 Nov 25;12(47):53257-53273. doi: 10.1021/acsami.0c15049. Epub 2020 Nov 16.
A supramolecular [2]pseudo-rotaxane containing a naphthalimide-based pillararene host and a spiropyran-based imidazole guest was synthesized and investigated in a semiaqueous solution with 90% water fraction. Upon UV exposure, the close-form structure of nonemissive spiropyran guest could be transformed into the open-form structure of red-emissive merocyanine guest reversibly, which was utilized as a monofluorophoric sensor to detect copper(II) and cyanide ions. Moreover, the naphthalimide host as an energy donor with green photoluminescence (PL) emission at 505 nm was complexed with the merocyanine guest as an energy acceptor with red PL emission at 650 nm in 1:1 molar ratio to generate a [2]pseudo-rotaxane polymer, which was further verified by the diffusion coefficients of DOSY nuclear magnetic resonance (NMR) measurements. Due to the Förster resonance energy transfer (FRET) processes, the bifluorophoric [2]pseudo-rotaxane produced more efficient ratiometric PL behavior to induce a stronger red PL emission than that of the monofluorophoric guest; therefore, the PL sensor responses of the supramolecular [2]pseudo-rotaxane toward copper(II) and cyanide ions could be further amplified via the FRET-OFF processes to turn off red PL emission of the reacted merocyanine acceptor and to recover green PL emission of the naphthalimide donor. Accordingly, the best and prominent values of the limit of detection (LOD) for the host-guest detections toward Cu and CN were 0.53 and 1.34 μM, respectively. The highest red MC emission with the optimum FRET processes of [2]pseudo-rotaxane was maintained around room temperature (20-40 °C) in wide pH conditions (pH = 3-13), which can be utilized in the cell viability tests to prove the nontoxic and remarkable biomarker of [2]pseudo-rotaxane to detect Cu and CN in living cells. The developed FRET-OFF processes with ratiometric PL behavior of the bifluorophoric supramolecular [2]pseudo-rotaxane polymer will open a new avenue to the future applications of chemo- and biosensors.
合成了一种包含萘二甲酰亚胺基柱芳烃主体和螺吡喃基咪唑客体的超分子[2]准轮烷,并在水含量为90%的半水溶液中对其进行了研究。在紫外光照射下,无发射的螺吡喃客体的闭环结构可可逆地转变为红色发射的部花青客体的开环结构,该结构被用作单荧光团传感器来检测铜(II)离子和氰离子。此外,在505 nm处发射绿色光致发光(PL)的萘二甲酰亚胺主体作为能量供体,与在650 nm处发射红色PL的部花青客体作为能量受体以1:1的摩尔比络合,生成一种[2]准轮烷聚合物,这通过扩散排序光谱(DOSY)核磁共振(NMR)测量的扩散系数得到了进一步验证。由于Förster共振能量转移(FRET)过程,双荧光团[2]准轮烷产生了更有效的比率PL行为,从而诱导出比单荧光团客体更强的红色PL发射;因此,超分子[2]准轮烷对铜(II)离子和氰离子的PL传感器响应可通过FRET关闭过程进一步放大,以关闭反应的部花青受体的红色PL发射,并恢复萘二甲酰亚胺供体的绿色PL发射。相应地,主客体检测中对铜和氰的检测限(LOD)的最佳和突出值分别为0.53和1.34 μM。在较宽的pH条件(pH = 3 - 13)下,[2]准轮烷具有最佳FRET过程的最高红色部花青发射在室温(20 - 40 °C)左右保持稳定,这可用于细胞活力测试,以证明[2]准轮烷在活细胞中检测铜和氰的无毒且显著的生物标志物特性。双荧光团超分子[2]准轮烷聚合物具有比率PL行为的FRET关闭过程的开发将为化学和生物传感器的未来应用开辟一条新途径。