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Synthesis and proton-conductive behaviour of two MOFs with covalently bonded imidazoles in the channels.

Kun-Peng ChenYue MaHong-Xia RenChen-Xi ZhangQing-Lun Wang
Published in: Dalton transactions (Cambridge, England : 2003) (2024)
Immobilization of imidazole molecules as proton carriers into MOFs to facilitate proton conduction is a general strategy for developing high proton conductive materials. Herein, we designed two imidazole substituted phthalic acid ligands and constructed two novel MOFs, {[Zr 6 (OH) 16 (H 3 L 1 ) 4 ]Cl 8 ·20H 2 O} n [Zr-MOF; H 3 L 1 = 2-(1 H -imidazol-4-yl) methylaminoterephthalic acid] and {Gd(HCOO)(H 2 L 2 ) 2 } n [Gd-MOF; H 3 L 2 = 5-(1 H -imidazol-4-yl)methylaminoisophthalic acid] and fully studied their porous nature, stability and water-assisted proton conduction. The resulting Zr-MOF exhibits a high proton conductivity of 1.82 × 10 -2 S cm -1 at 98% RH and 80 °C, while Gd-MOF has a proton conductivity of 3.01 × 10 -3 S cm -1 at 98% RH and 60 °C.
Keyphrases
  • metal organic framework
  • electron transfer
  • molecular docking
  • tissue engineering
  • magnetic nanoparticles