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

Author

Listed:
  • Jian Su

    (Nanjing University)

  • Shuai Yuan

    (Texas A&M University)

  • Hai-Ying Wang

    (Nanjing University)

  • Lan Huang

    (Texas A&M University)

  • Jing-Yuan Ge

    (Nanjing University)

  • Elizabeth Joseph

    (Texas A&M University)

  • Junsheng Qin

    (Texas A&M University)

  • Tahir Cagin

    (Texas A&M University
    Texas A&M University)

  • Jing-Lin Zuo

    (Nanjing University)

  • Hong-Cai Zhou

    (Texas A&M University
    Texas A&M University)

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.

Suggested Citation

  • Jian Su & Shuai Yuan & Hai-Ying Wang & Lan Huang & Jing-Yuan Ge & Elizabeth Joseph & Junsheng Qin & Tahir Cagin & Jing-Lin Zuo & Hong-Cai Zhou, 2017. "Redox-switchable breathing behavior in tetrathiafulvalene-based metal–organic frameworks," Nature Communications, Nature, vol. 8(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-02256-y
    DOI: 10.1038/s41467-017-02256-y
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