A Redox-Active Bistable Molecular Switch Mounted inside a Metal–Organic Framework
Qishui Chen, Junling Sun, Peng Li, Idan Hod, Peyman Z. Moghadam, Zachary S. Kean, Randall Q. Snurr, Joseph T. Hupp, Omar K. Farha, James Fraser Stoddart
Abstract
Qishui Chen, Junling Sun, Peng Li, Idan Hod, Peyman Z. Moghadam, Zachary S. Kean, Randall Q. Snurr, Joseph T. Hupp, Omar K. Farha, James Fraser Stoddart
Abstract
We describe the incorporation of a bistable mechanically interlocked molecule (MIM) into a robust Zr-based metal-organic framework (MOF), NU-1000, by employing a post-synthetic functionalization protocol. On average, close to two bistable [2]catenanes can be incorporated per repeating unit of the hexagonal channels of NU-1000. The reversible redox-switching of the bistable [2]catenanes is retained inside the MOF, as evidenced by solid-state UV-vis-NIR reflectance spectroscopy and cyclic voltammetry. This research demonstrates that bistable MIMs are capable of exhibiting robust dynamics inside the nanopores of a MOF.
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We describe the incorporation of a bistable mechanically interlocked molecule (MIM) into a robust Zr-based metal-organic framework (MOF), NU-1000, by employing a post-synthetic functionalization protocol. On average, close to two bistable [2]catenanes can be incorporated per repeating unit of the hexagonal channels of NU-1000. The reversible redox-switching of the bistable [2]catenanes is retained inside the MOF, as evidenced by solid-state UV-vis-NIR reflectance spectroscopy and cyclic voltammetry. This research demonstrates that bistable MIMs are capable of exhibiting robust dynamics inside the nanopores of a MOF.
Key concepts: Bistability, Chemistry, Catenane, Molecular switch, Redox, Nanopore, Cyclic voltammetry, Metal