Hydrogen-Bonding Linkers Yield a Large-Pore, Non-Catenated, Metal-Organic Framework with pcu Topology
Autor: | Tendai Gadzikwa, Victor W. Day, Mohammad S. Yazdanparast |
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Rok vydání: | 2019 |
Předmět: |
Materials science
Surface Properties Pharmaceutical Science hydrogen-bonding mixed-ligand 010402 general chemistry Topology 01 natural sciences Analytical Chemistry lcsh:QD241-441 Catenation Paddle wheel lcsh:Organic chemistry Drug Discovery Low density non-catenated large-pore Physical and Theoretical Chemistry pillared Topology (chemistry) Metal-Organic Frameworks Molecular Structure 010405 organic chemistry Hydrogen bond Communication Organic Chemistry Hydrogen Bonding metal-organic framework 0104 chemical sciences Large pore Chemistry (miscellaneous) Yield (chemistry) Molecular Medicine Metal-organic framework Adsorption paddle-wheel Porosity |
Zdroj: | Molecules Molecules, Vol 25, Iss 3, p 697 (2020) |
ISSN: | 1420-3049 |
Popis: | Pillared paddle-wheel-based metal-organic framework (MOF) materials are an attractive target as they offer a reliable method for constructing well-defined, multifunctional materials. A drawback of these materials, which has limited their application, is their tendency to form catenated frameworks with little accessible volume. To eliminate this disadvantage, it is necessary to investigate strategies for constructing non-catenated pillared paddle-wheel MOFs. Hydrogen-bonding substituents on linkers have been postulated to prevent catenation in certain frameworks and, in this work, we present a new MOF to further bolster this theory. Using 2,2′-diamino-[1,1′-biphenyl]-4,4′-dicarboxylic acid, BPDC-(NH2)2, linkers and dipyridyl glycol, DPG, pillars, we assembled a MOF with pcu topology. The new material is non-catenated, exhibiting large accessible pores and low density. To the best of our knowledge, this material constitutes the pcu framework with the largest pore volume and lowest density. We attribute the lack of catenation to the presence of H-bonding substituents on both linkers. |
Databáze: | OpenAIRE |
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