Knoevenagel冷凝
配体(生物化学)
丙二腈
苯甲醛
产量(工程)
化学
冷凝
气体分离
化学工程
选择性
金属有机骨架
多孔性
多孔介质
钇
多相催化
连接器
组合化学
材料科学
有机化学
高分子化学
合理设计
热稳定性
聚合物
纳米技术
过滤(数学)
缩合反应
热的
缩聚物
纳米材料
氧气
催化作用
原材料
模板
纳米笼
绿色化学
作者
Jincheng Si,Kang Zhou,Xin Zhou,Shuyu Xie,Xueliang Qin,Baobing Tang,Xueyue Yu,Hai‐Lun Xia,Hao Wang,Yunling Liu
标识
DOI:10.1021/acs.cgd.5c00706
摘要
Rare-earth metal–organic frameworks (RE-MOFs) have garnered significant attention in materials chemistry owing to their structural diversity and programmable functionality. The judicious selection of organic ligands plays a vital role in constructing novel RE-MOF architectures. JLU-MOF207 was constructed by using [Y4(μ3-O)2(HCOO)2] secondary building units (SBUs) with a methanetetrakis(p-biphenylcarboxylate) (H4MTBC) ligand and possessed an unprecedented (4, 4, 12) connected topology. Notably, the interweaving of helical Y–O chains and H4MTBC ligands within JLU-MOF207 generates ultramicroporous channels (∼ 5 Å diameter), which are decorated with exposed yttrium sites and oxygen-rich environments. JLU-MOF207 exhibits excellent acid, base, solvent, and thermal stability. Due to its confined spaces, multiple open yttrium sites, and oxygen donors in the helical ultramicroporous channels, JLU-MOF207 displays pronounced C3H6/C2H4 separation selectivity (9.6 at 298 K) and excellent production of 2-benzylidenemalononitrile with 99% yield from benzaldehyde and malononitrile at ambient temperature. The recorded turnover number (TON = 660) and turnover frequency (TOF = 5.5 min–1) surpass those of most reported MOF-based catalysts for Knoevenagel condensation. This study demonstrates that rational ligand design enables the construction of Y-MOF with dual functionality, providing new perspectives for developing multifunctional porous materials in gas separation and heterogeneous catalysis applications.
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