4.7 Article

A new multi-functional Cu(II)-organic framework as a platform for selective carbon dioxide chemical fixation and separation of organic dyes

Journal

CRYSTENGCOMM
Volume 23, Issue 47, Pages 8315-8322

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ce01274f

Keywords

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Funding

  1. Shaanxi Provincial Education Department [21JK0648]
  2. Young Talent Fund of Xi'an Association for Science and Technology [095920211325]
  3. Research Start-up Foundation of Xi'an Polytechnic University [BS201949]
  4. NSF of Shaanxi Province [2021JQ-666]
  5. China Postdoctoral Science Foundation [2020M673621XB]
  6. Young Talent Fund of University Association for Science and Technology in Shaanxi, China [20190608]
  7. Open Foundation of Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, China [KLSNFM2020006]
  8. Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education [LYJ2101]

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A new multi-functional metal-organic framework was synthesized using an asymmetrical V-shaped rigid multicarboxylic acid ligand and Cu(II) ions, exhibiting high CO2 adsorption capacity and selective capture over CH4. Further research on chemical fixation of CO2 reveals excellent catalytic activity, while the framework also shows selective sorption towards the rhodamine B dye, providing a facile synthetic route for multifunctional materials.
A new multi-functional metal-organic framework, {[Cu-2(HL)(H2O)(2)]center dot NMP center dot 2H(2)O}(n) (1), was assembled by employing an asymmetrical V-shaped rigid multicarboxylic acid ligand H5L (H5L = 2,4-di(2 ',5 '-dicarboxylphenyl)benzoic acid) with Cu(II) ions. 1 possesses a 3D pore formed by two types of intersecting 1D cuboid channels. Moreover, owing to the abundant uncoordinated carboxylate O atoms decorated in the channels and open metal centers generated by the removal of coordinated water molecules, 1 exhibits a high CO2 adsorption capacity and significantly selective capture for CO2 over CH4. Hence, further research on the chemical fixation of CO2 is implemented, which reveals excellent heterogeneous catalytic activity. In addition, 1 displays particularly selective sorption towards the rhodamine B (RB) dye. Consequently, this study may provide a facile synthetic route for the construction of multi-functional materials.

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