Abstract
Ir(ĈN)2(X̂N) derivatives showed remarkable photochemical properties, making them highly adaptable in the field of photocatalysis. By integration of [Ir(ppy)2]+ units into the quinoline-linked covalent organic frameworks Q-COF containing (N̂N) coordination sites, a wider spectral response range is achieved, leading to the development of unique entities with fascinating photophysical characteristics. The addition of Pt0 further enhances the performance of [Ir(ppy)2(N̂N)+Pt]@Q-COF for photocatalytic hydrogen evolution reaction, with the in situ utilization of photogenerated H2 enabling efficient nitro reduction.
Original language | English |
---|---|
Pages (from-to) | 16212-16218 |
Number of pages | 7 |
Journal | ACS Sustainable Chemistry and Engineering |
Volume | 12 |
Issue number | 44 |
DOIs | |
Publication status | Published - 4 Nov 2024 |
Keywords
- covalent organic framework
- cyclometalated Ir
- photocatalytic hydrogen evolution reaction
- photocatalytic nitro reduction
- platinum loading