配位聚合物
催化作用
化学
猝灭(荧光)
单斜晶系
组合化学
聚合物
反应速率常数
配位复合体
发光
动力学
荧光
超分子化学
配体(生物化学)
热液循环
氢键
纳米技术
化学工程
水热合成
制氢
金属有机骨架
无机化学
配位几何学
氢
化学动力学
材料科学
作者
Vibhav Shukla,Saman Shaheen,Tokeer Ahmad,Musheer Ahmad,Anil Kumar Astakala,Nohyun Lee,Nazrul Haq,Na'il Saleh,Kafeel Ahmad Siddiqui
标识
DOI:10.1021/acs.cgd.6c00344
摘要
A multifunctional gadolinium-based coordination polymer, [Gd(Cei)(H2O)]n+ (Gd-CP), constructed from bis(2-carboxyethyl) isocyanurate (H2Cei), was synthesized via a hydrothermal strategy and structurally characterized by single-crystal X-ray diffraction. The framework crystallizes in the monoclinic C2/c space group, where eight-coordinated Gd3+ centers adopt a distorted square-antiprismatic geometry to form a robust coordination network. The material exhibits efficient catalytic activity toward water splitting, delivering visible-light-driven hydrogen evolution with a cumulative H2 production of 28.52 mmol g–1 and a rate of 7.13 mmol h–1 g–1, along with promising electrocatalytic activity for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) with favorable kinetics and good durability. The increasing presence of antibiotic and pharmaceutical residues in aquatic environments necessitates rapid and sensitive monitoring approaches. In this regard, Gd-CP functions as a selective luminescent sensor for riboflavin (RBF) and colchicine (COL), exhibiting strong fluorescence quenching with Stern–Volmer constants of 3.1 × 104 M–1 and low detection limits of 1.430 and 1.158 ppm, respectively. These findings highlight Gd-CP as a versatile platform integrating water-splitting catalysis and pharmaceutical sensing within a single coordination framework.
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