深铬移
噻唑
水溶液
化学
荧光
检出限
聚合物
离子
猝灭(荧光)
缓冲溶液
无机化学
物理化学
立体化学
有机化学
色谱法
物理
量子力学
作者
Xin Li,Deping Xiu,Junjie Shi,Jiaran Miao,Yingying Yu,Hui‐Hua Song,Jin Lin,Qi Feng,Haitao Yu
标识
DOI:10.1016/j.saa.2021.120367
摘要
Abstract A new fluorescence coordination polymer [Zn(Py2TTz)(5-OH-IPA)]n (1) (Py2TTz = 2,5-bis(4-pyridyl)thiazolo[5,4-d]thiazole, 5-OH-IPA = 5-hydroxyisophthalic acid dianion) was synthesized, which exhibited the characteristics of fluorescence quenching and bathochromic shift toward Hg(II) in aqueous solution at pH 7.00. Mechanism study showed that the interactions between Hg(II) ions and Py2TTz ligands in 1 were responsible for the fluorescence emission change. Thanks to the specific interactions between 1 and Hg(II), excellent selectivity was achieved both in aqueous solution and in solid test paper. The detection limit of 1 for Hg(II) sensing was 125.76 nmol L−1 and a linear rang was 1.00–10.00 μmol L−1. More importantly, satisfactory recovery and accuracy of 1 for Hg(II) sensing were also obtained in buffer-free real water samples.
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