纳米孔
催化作用
氨基三乙酸
位阻效应
过渡金属
八面体
材料科学
纳米线
金属有机骨架
结晶学
试剂
纳米技术
化学
晶体结构
无机化学
螯合作用
立体化学
物理化学
有机化学
吸附
作者
Hao Luo,Cong Lin,Yang-En You,Xue Zhang,Jian Li,Lei Zhang,Junliang Sun,Zidong Wei,Jin‐Song Hu
出处
期刊:Matter
[Elsevier]
日期:2023-10-01
卷期号:6 (10): 3598-3607
被引量:3
标识
DOI:10.1016/j.matt.2023.08.002
摘要
Exploring metal-organic frameworks (MOFs) with specific structures is of great interest in both theoretical studies and practical applications. Herein, using a commercial achiral reagent (nitrilotriacetic acid [H3NTA]), a nanoporous MOF family, M(II)3(NTA)2 (M = Co, Fe, Mn; M-NTA), is discovered in the form of ultralong single-crystalline nanowires. It possesses an extraordinary structure with a very rare seven-coordination pattern (MO6N) for metal ions and an unprecedented chiral 3D transition metal-oxo framework constructed by edge-shared MO6N decahedra and MO6 octahedra. M-NTA shows excellent activity and selectivity in catalytic hydroboration of alkynes, and M−O in MO6 is the theoretical catalytic active site that is assisted by the possible structural steric effect between the activated MO6 and two adjacent MO6N polyhedra. These findings indicate that the M-NTA family not only enriches the structural diversity of MOF materials but that it also shows potential for catalytic organic conversion.
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