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Incorporation of Ir(C^N)(N^N)-NiCl in a (N^N)-covalent organic framework for transcendent dual catalysis in photochemical cross-coupling synthesis
Ist Teil von
Journal of materials chemistry. A, Materials for energy and sustainability, 2024-04, Vol.12 (15), p.9164-9172
Erscheinungsjahr
2024
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
A quinoline-based covalent organic framework (N^N)-
Q-COF
was constructed with chemically stable networks and (N^N)-sites. Its coordination bond with Ir(C^N)
2
(N^N) units generated new entities with exciting photophysical properties; particularly, the incorporation of a coumarin ligand greatly elevated its properties to a higher level. The further anchoring of NiCl
2
produced structures merging both photoredox and organometallic catalysts, resulting in excellent photocatalytic activities in C-S and C-N cross-coupling synthesis. The organic integration of Ir(C^N)
2
(N^N), NiCl
2
, and COFs and the advantages of COF networks were responsible for this transcendent dual catalysis. The chemical stability of Q-COFs and the coordination anchoring of Ir(C^N)
2
(N^N) and NiCl
2
enabled its recycling and reuse with no reduction in catalytic performance.
The incorporation of Ir(C^N)
2
(N^N)-NiCl
2
in quinoline-based (N^N)-covalent organic framework exhibits remarkable photocatalytic activities in cross-coupling synthesis.
Sprache
–
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/d4ta00443d
Titel-ID: cdi_rsc_primary_d4ta00443d
Format
–
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