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Acridine functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C–N cross-coupling

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Gisbertz,  Sebastian
Bartholomäus Pieber, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Reischauer,  Susanne
Bartholomäus Pieber, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Pieber,  Bartholomäus
Bartholomäus Pieber, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Citation

Traxler, M., Gisbertz, S., Pachfule, P., Schmidt, J., Roeser, J., Reischauer, S., et al. (2022). Acridine functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C–N cross-coupling. Angewandte Chemie International Edition, 61(21): e202117738. doi:10.1002/anie.202117738.


Cite as: http://hdl.handle.net/21.11116/0000-000A-0A03-8
Abstract
Covalent organic frameworks (COFs) are structurally tuneable, porous and crystalline polymers constructed through the covalent attachment of small organic building blocks as elementary units. Using the myriad of such building blocks, a broad spectrum of functionalities has been applied for COF syntheses for broad applications, including heterogeneous catalysis. Herein, we report the synthesis of a new family of porous and crystalline COFs using a novel acridine linker and benzene-1,3,5-tricarbaldehyde derivatives bearing a variable number of hydroxy groups. With the broad absorption in the visible light region the COFs were applied as photocatalysts in metallaphotocatalytic C–N cross coupling. The fully β-ketoenamine linked COF showed the highest activity, due to the increased charge separation upon irradiation. The COF showed good to excellent yields for several aryl bromides, good recyclability and even catalysed the organic transformation in presence of green light as energy source.