Unveiling the Unique Roles of Metal Coordination and Modulator in the Polymorphism Control of Metal‐Organic Frameworks
Zi‐Jian Li, Yu Ju, Zeya Zhang, Huangjie Lu, Yongxin Li, Ningjin Zhang, Xian‐Long Du, Xiaofeng Guo, Zhi‐Hui Zhang, Yuan Qian, Mingyang He, Jian‐Qiang Wang, Jian Lin
Abstract
Abstract Polymorphism control of metal‐organic frameworks is highly desired for elucidating structure‐property relationships, but remains an empirical process and is usually done in a trial‐and‐error approach. We adopted the rarely used actinide cation Th 4+ and a ditopic linker to construct a series of thorium‐organic frameworks (TOFs) with a range of polymorphs. The extraordinary coordination versatility of Th 4+ cations and clusters, coupled with synthetic modulation, gives five distinct phases, wherein the highest degree of interpenetration (threefold) and porosity (75.9 %) of TOFs have been achieved. Notably, the O atom on the capping site of the nine‐coordinated Th 4+ cation can function as a bridging unit to interconnect neighboring secondary building units (SBUs), affording topologies that are undocumented for other tetravalent‐metal‐containing MOFs. Furthermore, for the first time HCOOH has been demonstrated as a bridging unit of SBUs to further induce structural complexity. The resulting TOFs exhibit considerably different adsorption behaviors toward organic dyes, thus suggesting that TOFs represent an exceptional and promising platform for structure‐property relationship study.