Vinylene‐Linked Covalent Organic Frameworks (COFs) with Symmetry‐Tuned Polarity and Photocatalytic Activity.

Xu, Junsong; Yang, Can; Bi, Shuai; Wang, Wenyan; He, Yafei; Wu, Dongqing; Liang, Qifeng; Wang, Xinchen; Zhang, Fan

The polarity of a semiconducting molecule affects its intrinsic photophysical properties, which can be tuned by varying the molecular geometry. Herein, we developed a D3h‐symmetric tricyanomesitylene as a new monomer which could be reticulated into a vinylene‐linked covalent organic framework (g‐C54N6‐COF) via Knoevenagel condensation with another D3h‐symmetric monomer 2,4,6‐tris(4′‐formyl‐biphenyl‐4‐yl)‐1,3,5‐triazine. Replacing tricyanomesitylene with a C2v‐symmetric 3,5‐dicyano‐2,4,6‐trimethylpyridine gave a less‐symmetric vinylene‐linked COF (g‐C52N6‐COF). The octupolar conjugated characters of g‐C54N6‐COF were reflected in its scarce solvatochromic effects either in ground or excited states, and endowed it with more promising semiconducting behavior as compared with g‐C52N6‐COF, such as enhanced light‐harvesting and excellent photo‐induced charge generation and separation. Along with the matched energy level, g‐C54N6‐COF enabled the two‐half reactions of photocatalytic water splitting with an average O2 evolution rate of 51.0 μmol h−1 g−1 and H2 evolution rate of 2518.9 μmol h−1 g−1. Such values are among the highest of state‐of‐the‐art COF photocatalysts.

MOLECULAR shapes; SOLVATOCHROMISM; TRIAZINES; EXCITED states; MONOMERS; CONDENSATION; POLARITY (Chemistry)

Angewandte Chemie, 2020, Vol 132, Issue 52, p24053

0044-8249

Academic Journal

10.1002/ange.202011852