羧酸盐
微型多孔材料
化学
介孔材料
配体(生物化学)
联氨(抗抑郁剂)
化学吸附
氧化还原
材料科学
吸附
合理设计
超分子化学
水合物
红外光谱学
化学工程
化学稳定性
纳米技术
光谱学
工作(物理)
非共价相互作用
衍射
催化作用
无机化学
分子
粉末衍射
X射线晶体学
晶体结构
作者
Yong‐Zheng Zhang,Tao He,Xiang‐Jing Kong,Yingjie Wang,Lin‐Hua Xie,Jian‐Rong Li
标识
DOI:10.1002/anie.202522510
摘要
Expanding pyrazolate metal-organic frameworks (MOFs) beyond microporous architectures is a formidable synthetic challenge, as the strong and directional M-N bonds impose strict geometric constraints that hinder the integration of mesoporosity and active sites. Such limitations have restricted the structural diversity of pyrazolate MOFs compared with their carboxylate analogues, despite the former offering superior chemical stability and fantastic performance in gas storage, separation, and catalysis. Here we present mesoporous BUT-45 as the first example of csq-type pyrazolate MOF, which was constructed from the low-symmetry (Cs) tetra-pyrazolate ligand 1,3,6,8-tetra(1H-pyrazolate-4-yl)-9H-carbazole (CTP4-) and 8-connected Co6 clusters (D2h). Interestingly, the presence of rich active Co sites enables instantaneous O2 chemisorption at ambient temperature in BUT-45, and good framework stability allows this process to be fully reversible. Single-crystal x-ray diffraction and in situ spectroscopy analyses provide structural insights into the as-synthesized, O2-loaded, and regenerated phases, revealing the mechanism of Co-O2 adduct formation and demonstrating complete reversibility via hydrazine hydrate reduction. This work highlights how reticular chemistry can map target nets from carboxylate to pyrazolate, while offering desired properties and direct visualization of redox chemistry in MOFs.
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