Phenyl Extended Naphthalene-Based Covalent Triazine Frameworks as Versatile Metal-Free Heterogeneous Photocatalysts

Two new covalent triazines frameworks (CTFs) containing phenyl extended naphthalene units (with and without methoxy groups in the naphthalene core) are prepared by thermal and microwave activation. Both procedures yield similar chemical structures combining triazine acceptor units with donor aromatic groups, but they generate some differences in the morphology, structural organization, CO2 adsorption capacity, and thermal and optical properties. Besides, the methoxy groups of the naphthalene core have also influence in some of these properties. The resulting phenyl extended naphthalene CTFs are efficiently utilized as metal-free heterogeneous photocatalyst for the selective aerobic oxidation of sulfides and the dehydrogenative cross-coupling reactions under visible-light irradiation, showing a high chemical stability.

Automated summary

Two new covalent triazine frameworks incorporating phenyl extended naphthalene units have been prepared using thermal and microwave activation. These frameworks show similar chemical structures but exhibit differences in morphology, structural organization, CO2 adsorption capacity, and thermal and optical properties. Additionally, the presence of methoxy groups in the naphthalene core has an influence on some of these properties. The resulting phenyl extended naphthalene CTFs are utilized as metal-free heterogeneous photocatalysts for selective reactions under visible-light irradiation, demonstrating high chemical stability.