Programmable Photocatalytic Activity of Multicomponent Covalent Organic Frameworks Used as Metallaphotocatalysts

Abstract: The multicomponent approach allows to incorporate several functionalities into a single covalent organic framework (COF) and consequently allows the construction of bifunctional materials for cooperative catalysis. The well‐defined structure of such multicomponent COFs is furthermore ideally suited for structure‐activity relationship studies. We report a series of multicomponent COFs that contain acridine‐ and 2,2’‐bipyridine linkers connected through 1,3,5‐benzenetrialdehyde derivatives. The acridine motif is responsible for broad light absorption, while the bipyridine unit enables complexation of nickel catalysts. These features enable the usage of the framework materials as catalysts for light‐mediated carbon−heteroatom cross‐couplings. Variation of the node units shows that the catalytic activity correlates to the keto‐enamine tautomer isomerism. This allows switching between high charge‐carrier mobility and persistent, localized charge‐separated species depending on the nodes, a tool to tailor the materials for specific reactions. Moreover, nickel‐loaded COFs are recyclable and catalyze cross‐couplings even using red light irradiation.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Programmable Photocatalytic Activity of Multicomponent Covalent Organic Frameworks Used as Metallaphotocatalysts ; day:01 ; month:12 ; year:2022 ; extent:1
Chemistry - a European journal ; (01.12.2022) (gesamt 1)

Urheber
Traxler, Michael
Reischauer, Susanne
Vogl, Sarah
Roeser, Jérôme
Rabeah, Jabor
Penschke, Christopher
Saalfrank, Peter
Pieber, Bartholomäus
Thomas, Arne

DOI
10.1002/chem.202202967
URN
urn:nbn:de:101:1-2022120214031150160235
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:21 MESZ

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