化学
卤素
共晶
碘化物
离子
卤键
检出限
卤化物
电化学发光
化学物理
分析化学(期刊)
纳米技术
分子
无机化学
氢键
有机化学
环境化学
烷基
材料科学
色谱法
作者
Qiong Wu,Qiao‐Qiao Jiang,Yajie Li,Yingao Wang,Xun Wang,Ru‐Ping Liang,Jian‐Ding Qiu
标识
DOI:10.1021/acs.analchem.3c05632
摘要
Developing new electrochemiluminescence (ECL) luminators with high stability, wide applicability, and strong designability is of great strategic significance to promote the ECL field to the frontier. Here, driven by the I···N bond, 1,3,5-trifluoro-2,4,6-triiodobenzene (TFTI) and 2,4,6-trimethyl-1,3,5-triazine (TMT) self-assembled into a novel halogen cocrystal (TFTI-TMT) through slow solution volatilization. Significant difference of charge density existed between the N atoms on TMT and the σ-hole of the I atoms on TFTI. Upon the induction of σ-hole effect, high-speed and spontaneous charge transferring from TMT to the σ-hole of TFTI occurred, stimulating exciting ECL signals. Besides, the σ-hole of the I atoms could capture iodine ions specifically, which blocked the original charge transfer from the N atoms to the σ-hole, causing the ECL signal of TFTI-TMT to undergo a quenching rate as high as 92.9%. Excitingly, the ECL sensing of TFTI-TMT toward I– possessed a wide linear range (10–5000 nM) and ultralow detection limit (3 nM) in a real water sample. The halogen cocrystal strategy makes σ-hole a remarkable new viewpoint of ECL luminator design and enables ECL analysis technology to contribute to addressing the environmental and health threats posed by iodide pollution.
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