4.8 Article

In Situ Investigation of Multicomponent MOF Crystallization during Rapid Continuous Flow Synthesis

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 45, 页码 54284-54293

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c04920

关键词

metal-organic frameworks; X-ray diffraction; synthetic methods; crystal growth; adsorption

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Rapid synthesis of phase pure and highly crystalline multicomponent MOFs can be achieved using continuous flow chemistry. Key differences in the formation mechanisms between ternary UMCM-1 and quaternary MUF-7 have been uncovered, providing insights into MOFs formation.
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, in situ 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-S, 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.

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