4.8 Article

Fabrication of Hydrazone-Linked Covalent Organic Frameworks Using Alkyl Amine as Building Block for High Adsorption Capacity of Metal Ions

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 12, Pages 11706-11714

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b18502

Keywords

flexible alkyl amine; covalent organic frameworks; intramolecular hydrogen bonding; metal ions adsorption; high capacity; selectivity adsorption

Funding

  1. China State Key Basic Research Program Grant [2016YFA0501402]
  2. National Science Fund for Distinguished Young Scholars [21525524]
  3. National Natural Sciences Foundation of China [21575141]
  4. CAS-Weigao Research & Development Program [[2017]-009]

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There are several researches on the preparation and application of hydrazone-linked covalent organic frameworks (COFs), and all of them generally necessitate rigid aromatic amines. Herein, we report a strategy for design and synthesis of COF with flexible alkyl amine as a building block and intramolecular hydrogen bonding as a knot in the network. The proof-of-concept design was demonstrated by exploring 1,3,5-triformylphloroglucinol and oxalyldihydrazide (ODH) as precursors to synthesize a novel COF material (TpODH), in which different organic building units are combined through hydrazone bonds to form two-dimensional porous frameworks. It should be pointed that irreversible enol-to-keto tautomerism and intramolecular N-H center dot center dot center dot O=C hydrogen bonding of TpODH would enhance the crystallinity and chemical stability, leading to large specific surface area of 835 m(2) g(-1). However, another COF synthesized with 1,3,5-triformylbenzene and ODH exhibited less crystallinity and low special surface area (94 m(2) g(-1)). Representatively, the resulting TpODH afforded Cu(II) and Hg(II) capacities of 324 and 1692 mg g(-1), respectively, which exceeded that of most COFs previously reported. Moreover, the Fourier-transform infrared and X-ray photoelectron spectroscopy spectra analyses were taken to demonstrate the adsorption mechanism. These results suggested that the materials could be applied to the removal of metallic ions in the future.

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