双金属片
材料科学
结晶学
锆
金属有机骨架
抗磁性
连接器
单晶
钴
纳米技术
拓扑(电路)
金属
化学
磁场
物理化学
物理
吸附
冶金
组合数学
操作系统
量子力学
计算机科学
数学
作者
Shuai Yuan,Jun‐Sheng Qin,Jian Su,Bao Li,Jialuo Li,Wenmiao Chen,Hannah F. Drake,Peng Zhang,Daqiang Yuan,Jing‐Lin Zuo,Hong‐Cai Zhou
标识
DOI:10.1002/ange.201808568
摘要
Abstract Heterometallic metal–organic frameworks (MOFs) allow the precise placement of various metals at atomic precision within a porous framework. This new level of control by MOFs promises fascinating advances in basic science and application. However, the rational design and synthesis of heterometallic MOFs remains a challenge due to the complexity of the heterometallic systems. Herein, we show that bimetallic MOFs with MX 2 (INA) 4 moieties (INA=isonicotinate; M=Co 2+ or Fe 2+ ; X=OH − , Cl − , Br − , I − , NCS − , or NCSe − ) can be generated by the sequential modification of a Zr‐based MOF. This multi‐step modification not only replaced the linear organic linker with a square planar MX 2 (INA) 4 unit, but also altered the symmetry, unit cell, and topology of the parent structure. Single‐crystal to single‐crystal transformation is realized so that snapshots for transition process were captured by successive single‐crystal X‐ray diffraction. Furthermore, the installation of Co(NCS) 2 (INA) 4 endows field‐induced slow magnetic relaxation property to the diamagnetic Zr‐MOF.
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