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Dramatic improvement of stability by in situ linker cyclization of a metal-organic framework. | LitMetric

AI Article Synopsis

  • * The process starts with assembling the MOF and then inducing thermocyclization to create fused-aromatic bridges within the structure, which maintains its crystal order.
  • * This cyclization reinforces the structural integrity of the MOF and boosts its electroactivity and charge transport capabilities across the network.

Article Abstract

We employ a two-step strategy for accessing crystalline porous covalent networks of highly conjugated π-electron systems. For this, we first assembled a crystalline metal-organic framework (MOF) precursor based on Zr(iv) ions and a linear dicarboxyl linker molecule featuring backfolded, highly unsaturated alkyne backbones; massive thermocyclization of the organic linkers was then triggered to install highly conjugated, fused-aromatic bridges throughout the MOF scaffold while preserving the crystalline order. The formation of cyclized carbon links not only greatly strengthens the precursor coordination scaffold, but also, more importantly, enhances electroactivity and charge transport throughout the polycyclic aromatic grid.

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Source
http://dx.doi.org/10.1039/c8cc05225eDOI Listing

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