4.8 Article

Redox-switchable breathing behavior in tetrathiafulvalene-based metal-organic frameworks

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-02256-y

Keywords

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Funding

  1. Major State Basic Research Development Program [2013CB922101]
  2. National Natural Science Foundation of China [91433113, 21631006]
  3. Center for Gas Separations Relevant to Clean Energy Technologies, an Energy Frontier Research Center - US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001015]
  4. Hydrogen and Fuel Cell Program [DE-EE0007049]
  5. Robert A. Welch Foundation through a Welch Endowed Chair [A-0030]
  6. Distinguished Scientist Fellowship Program (DSFP) at KSU
  7. US Department of Energy Office of Fossil Energy, National Energy Technology Laboratory [DE-FE0026472]
  8. ConocoPhillips
  9. Dow Chemical Graduate Fellowship

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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 N-2. 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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