等结构
质子
荧光
电导率
化学
热传导
合理设计
光化学
间苯二甲酸
材料科学
化学物理
纳米技术
金属
结晶学
质子输运
调节器
电阻率和电导率
无机化学
离子
金属有机骨架
作者
Chen He,Zhenchang Zhu,Linlin Wang,Yanfeng He,Jun Hu,Jing-yuan Ge,Zhongyan Chen,Xiangchao Shi
标识
DOI:10.1021/acs.cgd.6c00024
摘要
Two isostructural three-dimensional metal–organic frameworks (MOFs), [Co(TTz)(IPA)]·0.5(TTz)·0.5H2O (HC-1) and [Cd(TTz)(IPA)]·0.5(TTz)·H2O (HC-2), were constructed via a dual-ligand strategy using ligands 2,5-bis(pyridin-4-yl)thiazolo[5,4-d]thiazole (TTz) and isophthalic acid (H2IPA). Both MOFs display selective, intrinsic ratiometric fluorescence responses toward glutathione, arising from pronounced emission enhancement accompanied by red-shifted maxima, enabling selective and sensitive GSH detection with limits of detection of 1.28 μM for HC-1 and 0.30 μM for HC-2. Notably, the ratiometric response is achieved within single-component MOFs without the need for composite architectures. In addition, the materials display humidity-dependent proton conduction behavior. HC-1 achieves a high proton conductivity of 1.80 × 10–4 S·cm–1 at 98% relative humidity and 338 K, whereas HC-2 shows a much lower proton conductivity of 5.30 × 10–6 S·cm–1 under identical conditions. Comparative studies reveal that the metal ion plays a decisive role in regulating both fluorescence signaling and proton transport, despite minimal structural perturbation. These findings demonstrate that metal-ion identity serves as a decisive regulator of fluorescence signaling and proton conduction in isostructural MOFs, providing mechanistic insight into the design of multifunctional crystalline materials.
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