聚合物
荧光
化学
转化(遗传学)
猝灭(荧光)
配体(生物化学)
光化学
水溶液
组合化学
配位聚合物
荧光光谱法
材料科学
乙醇
金属
金属有机骨架
分析化学(期刊)
分解
配位复合体
作者
Shaowen Qie,Yefang Yang,Zhilin Mu,Wenping Hu,Ruijie Xu,Wenting Li,Ling Yue,Jingjing Qiao,Ming Hu
标识
DOI:10.1021/acs.cgd.5c01560
摘要
The single-crystal to single-crystal transformation provides a precise strategy for regulating the functional properties of coordination polymers. In this work, [CdL(CH3CH2OH)(H2O)0.5]n (Cd-1) with a 2D network structure was synthesized based on 2,2′-thiobis-4-pyridinecarboxylic acid ligand (H2L); then, [CdL]n (Cd-2) with a 3D framework was accomplished through the single-crystal to single-crystal transformation under the stimulation of water molecules. Cd-1 and Cd-2 exhibited the ligand-centered emission peaks at 430, 466 nm and 416, 466 nm with the fluorescence lifetimes of 0.59 and 0.60 ns, respectively. Interestingly, Cd-1 showed fluorescence quenching in response to levofloxacin (LOFX) in ethanol solution, while Cd-2 exhibited a significant fluorescence enhancement effect in aqueous solution, in which these differentiated phenomena facilitated a contrastive identification of LOFX in practical applications. In addition, the detailed mechanism comparisons of their differential fluorescence response behaviors were further conducted. Notably, some portable detection devices based on Cd-2 had been developed for visual recognition of LOFX.
科研通智能强力驱动
Strongly Powered by AbleSci AI