Two-Dimensional Imine-Linked Covalent Organic Frameworks as a Platform for Selective Oxidation of Olefins

Two-dimensional imine-linked covalent organic frameworks with hydroxyl groups, <b>TAPT-DHTA-COF_HX</b> and <b>TAPT-DHTA-COF_DMF</b>, were respectively constructed by the condensation of 1,3,5-tris-(4-aminophenyl)­triazine and 2,5-dihydroxyl-terephthalaldehyde under solvothermal and reflux conditions. Both COFs possess excellent thermal stability and a similar eclipsed stacking structure verified by XRD patterns. However, <b>TAPT-DHTA-COF_HX</b> presented a larger surface area (2238 m²/g) and higher crystallinity than <b>TAPT-DHTA-COF_DMF</b>. Significantly, copper ions are efficiently incorporated into the pores of these two COFs via the coordination interaction with hydroxyl groups and imine linkers. The obtained copper-containing COFs (<b>Cu-COF_HX</b> and <b>Cu-COF_DMF</b>) were employed in the selective oxidation of styrene to benzaldehyde. <b>Cu-COF_HX</b> with superior surface area (1886 m²/g) and pore volume (1.11 cm³/g) exhibited excellent catalytic performance and recyclability. This strategy not only provides a convenient approach to design imine-linked 2D COFs with hydroxyl groups, but also develops their novel application for catalysis