Luminescent Two-Dimensional Metal–Organic Framework Nanosheets with Large π-Conjugated System: Design, Synthesis, and Detection of Anti-Inflammatory Drugs and Pesticides

纳米片 化学 共轭体系 组合化学 发光 双氯芬酸钠 氧化剂 配体(生物化学) 金属有机骨架 猝灭(荧光) 光化学 化学工程 有机化学 荧光 吸附 聚合物 材料科学 光电子学 受体 生物化学 物理 色谱法 量子力学 工程类
作者
Cai‐Xia Yu,Wen Jiang,Ke-Zhong Wang,Ai‐Ping Liang,Jian-Guo Song,Yanli Zhou,Xueqin Sun,Lei‐Lei Liu
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:61 (2): 982-991 被引量:33
标识
DOI:10.1021/acs.inorgchem.1c03040
摘要

Two-dimensional (2D) metal–organic framework (MOF) nanosheets, with largely exposed surface area and highly accessible active sites, have emerged as a novel kind of sensing material. Here, a luminescent 2D MOF nanosheet was designed and synthesized by a facile top-down strategy based on a three-dimensional (3D) layered MOF {[Zn(H2L)(H2O)2]·H2O}n (Zn-MOF; H4L = 3,5-bis(3′,5′-dicarboxyphenyl)-1H-1,2,4-triazole). With a large π-conjugated system and rigid planar structure, ligand H4L was elaborately selected to construct the bulk Zn-MOF, which can be readily exfoliated into 2D nanosheets, owing to the weak interlayer interactions and easy-to-release H2O molecules in the interspaces of 2D layers. Given the great threat posed to the ecological environment by anti-inflammatory drugs and pesticides, the developed luminescent Zn-MOF nanosheets were utilized to determine these organic pollutants, achieving highly selective and sensitive detection of diclofenac sodium (DCF) and tetramethylthiuram disulfide (TMTD). Compared to the detection limits of 3D Zn-MOF (7.72 ppm for DCF, 6.01 ppm for TMTD), the obviously lower detection limits for 2D Zn-MOF nanosheets toward DCF (0.20 ppm) and TMTD (0.18 ppm) further revealed that the largely exposed surface area with rigid planar structure and ultralarge π-conjugated system greatly accelerated electron transfer, which brought about a vast improvement in response sensitivity. The remarkable quenching performance for DCF and TMTD stems from a combined effect of photoinduced electron transfer and competitive energy absorption. The possible sensing mechanism was systematically investigated by the studies of powder X-ray diffraction, UV–vis, luminescence lifetime, and density functional theory calculations.
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