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Abstract
Metal–organic frameworks (MOFs) that respond to external stimuli such as guest molecules, temperature, or redox conditions are highly desirable. Herein, we coupled redox-switchable properties with breathing behavior induced by guest molecules in a single framework. Guided by topology, two flexible isomeric MOFs, compounds 1 and 2, with a formula of In(Me2NH2)(TTFTB), were constructed via a combination of [In(COO)4]− metal nodes and tetratopic tetrathiafulvalene-based linkers (TTFTB). The two compounds show different breathing behaviors upon the introduction of N2. Single-crystal X-ray diffraction, accompanied by molecular simulations, reveals that the breathing mechanism of 1 involves the bending of metal–ligand bonds and the sliding of interpenetrated frameworks, while 2 undergoes simple distortion of linkers. Reversible oxidation and reduction of TTF moieties changes the linker flexibility, which in turn switches the breathing behavior of 2. The redox-switchable breathing behavior can potentially be applied to the design of stimuli-responsive MOFs.
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1 State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing, China
2 Department of Chemistry, Texas A&M University, College Station, TX, USA
3 Department of Materials Science and Engineering, Texas A&M University, College Station, TX, USA
4 Department of Chemistry, Texas A&M University, College Station, TX, USA; Artie McFerrin Department of Chemical Engineering, Texas A&M University, College Station, TX, USA
5 Department of Chemistry, Texas A&M University, College Station, TX, USA; Department of Materials Science and Engineering, Texas A&M University, College Station, TX, USA