| Literature DB >> 30102004 |
Shuai Yuan1, Jun-Sheng Qin1, Jian Su2, Bao Li1, Jialuo Li1, Wenmiao Chen1, Hannah F Drake1, Peng Zhang1, Daqiang Yuan3, Jinglin Zuo2, Hong-Cai Zhou1,4.
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 MX2 (INA)4 moieties (INA=isonicotinate; M=Co2+ or Fe2+ ; 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 MX2 (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.Entities:
Keywords: heterometallic MOFs; metal-organic frameworks; postsynthetic modification; single-crystal to single-crystal transformation
Year: 2018 PMID: 30102004 DOI: 10.1002/anie.201808568
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336