Enhanced Energy Transfer in A π-Conjugated Covalent Organic Framework Facilitates Excited-State Nickel Catalysis

Covalent organic frameworks (COFs) have received broad interest owing to their permanent porosity, high stability, and tunable functionalities. COFs with long-range pi-conjugation and photosensitizing building blocks have been explored for sustainable photocatalysis. Herein, we report the first example of COF-based energy transfer Ni catalysis. A pyrene-based COF with sp(2) carbon-conjugation was synthesized and used to coordinate Ni-II centers through bipyridine moieties. Under light irradiation, enhanced energy transfer in the COF facilitated the excitation of Ni centers to catalyze borylation and trifluoromethylation reactions of aryl halides. The COF showed two orders of magnitude higher efficiency in these reactions than its homogeneous control and could be recovered and reused without significant loss of catalytic activity.

Automated summary

We report the first example of COF-based energy transfer Ni catalysis, where a pyrene-based COF was synthesized and used to coordinate Ni-II centers for efficient borylation and trifluoromethylation reactions of aryl halides under light irradiation. The COF showed two orders of magnitude higher efficiency than its homogeneous control and could be reused without significant loss of catalytic activity.