化学
碘化物
水溶液
铜
发光
无机化学
猝灭(荧光)
分解
配体(生物化学)
结晶学
荧光
物理化学
有机化学
受体
物理
量子力学
生物化学
光电子学
作者
Eunji Lee,Huiyeong Ju,Jong Hwa Jung,Mari Ikeda,Yoichi Habata,Shim Sung Lee
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2018-12-31
卷期号:58 (2): 1177-1183
被引量:37
标识
DOI:10.1021/acs.inorgchem.8b02549
摘要
Formation of a copper(I) iodide cluster based luminescent metal–organic frameworks (LMOFs) and its utilization for the detection of cysteine (Cys) in aqueous solution are reported. The reaction of bis(amidoquinoline) ligand (L) with copper(I) iodide afforded an LMOF {[(Cu2I2)L2]·2DMSO}n (1) with a 44-sql topology linked by Cu2I2 clusters as a thermodynamic product. Time- and temperature-dependent PXRD experiments confirmed that the entire formation process for 1 is kinetically and thermodynamically controlled. Interestingly, LMOF 1 was also obtained under the mechanochemical condition. Moreover, LMOF 1 dispersed in water shows a selective quenching for Cys over other amino acids due to the strong affinity of Cys to copper(I) iodide. On the basis of the NMR data of L isolated from the decomposition of 1, the decomposition–displacement mechanism was proposed for the sensing of Cys. This result might be utilized for the practical detection of Cys because the sensing material can be prepared simply, and the sensing process is performed in aqueous media.
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