He Brandon, Macreadie Lauren K, Gardiner James, Telfer Shane G, Hill Matthew R
Department of Chemical Engineering, Monash University, Clayton, VIC 3800, Australia.
CSIRO Private Bag 10, Clayton South, VIC 3169, Australia.
ACS Appl Mater Interfaces. 2021 Nov 17;13(45):54284-54293. doi: 10.1021/acsami.1c04920. Epub 2021 Nov 5.
Access to the potential applications of metal-organic frameworks (MOFs) depends on rapid fabrication. While there have been advances in the large-scale production of single-component MOFs, rapid synthesis of multicomponent MOFs presents greater challenges. Multicomponent systems subjected to rapid synthesis conditions have the opportunity to form separate kinetic phases that are each built up using just one linker. We sought to investigate whether continuous flow chemistry could be adapted to the rapid formation of multicomponent MOFs, exploring the UMCM-1 and MUF-77 series. Surprisingly, phase pure, highly crystalline multicomponent materials emerge under these conditions. To explore this, WAXS was undertaken to gain an understanding of the formation mechanisms at play during flow synthesis. Key differences were found between the ternary UMCM-1 and the quaternary MUF-7, and key details about how the MOFs form were then uncovered. Counterintuitively, despite consisting of just two ligands UMCM-1 proceeds via MOF-5, whereas MUF-7 consists of three ligands but is generated directly from the reaction mixture. By taking advantage of the scalable high-quality materials produced, C6 separations were achieved in breakthrough settings.
金属有机框架材料(MOFs)潜在应用的实现依赖于快速制备。虽然单组分MOFs的大规模生产已有进展,但多组分MOFs的快速合成面临更大挑战。在快速合成条件下的多组分体系有机会形成各自仅使用一种连接体构建的独立动力学相。我们试图研究连续流动化学是否可适用于多组分MOFs的快速形成,探索UMCM - 1和MUF - 77系列。令人惊讶的是,在这些条件下出现了相纯、高结晶度的多组分材料。为探究此现象,进行了广角X射线散射(WAXS)以了解流动合成过程中起作用的形成机制。在三元UMCM - 1和四元MUF - 7之间发现了关键差异,随后揭示了MOFs形成的关键细节。与直觉相反,尽管UMCM - 1仅由两种配体组成,但它通过MOF - 5生成,而MUF - 7由三种配体组成却是直接从反应混合物中生成。利用所制备的可扩展高质量材料,在突破实验中实现了C6分离。