Mechanical Tunability via Hydrogen Bonding in Metal-Organic Frameworks with the Perovskite Architecture.

Two analogous metal-organic frameworks (MOFs) with the perovskite architecture, [C(NH)][Mn-(HCOO)] (1) and [(CH)NH][Mn(HCOO)] (2), exhibit significantly different mechanical properties. The marked difference is attributed to their distinct modes of hydrogen bonding between the A-site amine cation an...

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Publicado en:Journal of the American Chemical Society Vol. 136; no. 22; pp. 7801 - 7805
Autores principales: Wei Li, Thirumurugan, A., Barton, Phillip T., Zheshuai Lin, Henke, Sebastian, Yeung, Hamish H.-M., Wharmby, Michael T., Bithell, Erica G., Howard, Christopher J., Cheetham, Anthony K.
Formato: Artículo
Publicado: American Chemical Society 6/4/2014
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Acceso en línea:Ver este registro en EBSCOhost
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        10.1021/ja500618z
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        atl: Mechanical Tunability via Hydrogen Bonding in Metal-Organic Frameworks with the Perovskite Architecture.
      aug:
        au:
          Wei Li
          Thirumurugan, A.
          Barton, Phillip T.
          Zheshuai Lin
          Henke, Sebastian
          Yeung, Hamish H.-M.
          Wharmby, Michael T.
          Bithell, Erica G.
          Howard, Christopher J.
          Cheetham, Anthony K.
        affil:
          Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FS, U.K.
          School of Chemistry, Indian Institute of Science Education and Research (IISER-TVM), Thiruvananthapuram, Kerala 695016, India
          Materials Research Laboratory (MRL) and Materials Department, University of California, Santa Barbara, California 93106, United States
          Beijing Center of Crystal R&D, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, P.O. Box 2711, Beijing 100080, P. R. China
          International Center for Young Scientists (ICYS), International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki 305-0044, Japan
          Institute of Continuing Education, University of Cambridge, Madingley Hall, Madingley, Cambridge CB23 8AQ, U.K.
          School of Engineering, University of Newcastle, Callaghan, New South Wales 2308, Australia
      su:
        Metal-organic frameworks
        Structural frames
        Perovskite
        Hydrogen bonding
        Molecular association
        Crystal chemical bonds
        Thermal expansion
      sug:
        subj:
          Metal-organic frameworks
          Structural frames
          Perovskite
          Hydrogen bonding
          Molecular association
          Crystal chemical bonds
          Thermal expansion
      ab: Two analogous metal-organic frameworks (MOFs) with the perovskite architecture, [C(NH)][Mn-(HCOO)] (1) and [(CH)NH][Mn(HCOO)] (2), exhibit significantly different mechanical properties. The marked difference is attributed to their distinct modes of hydrogen bonding between the A-site amine cation and the anionic framework. The stronger cross-linking hydrogen bonding in 1 gives rise to Young's moduli and hardnesses that are up to twice those in 2, while the thermal expansion is substantially smaller. This study presents clear evidence that the mechanical properties of MOF materials can be substantially tuned via hydrogen-bonding interactions.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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