Evidence map›Paper›PMID 36223495›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2023

Programmable Photocatalytic Activity of Multicomponent Covalent Organic Frameworks Used as Metallaphotocatalysts.

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

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Covalent Organic Frameworks for Photocatalysis.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  2. Review
  3. Cooperative Photoredox Catalysis Under Confinement.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Michael TraxlerDepartment of Chemistry/Functional Materials, Technische Universität Berlin, Hardenbergstraße 40, 10623, Berlin, Germany.
Susanne ReischauerDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Sarah VoglDepartment of Chemistry/Functional Materials, Technische Universität Berlin, Hardenbergstraße 40, 10623, Berlin, Germany.
Jérôme RoeserDepartment of Chemistry/Functional Materials, Technische Universität Berlin, Hardenbergstraße 40, 10623, Berlin, Germany.
Jabor RabeahLeibniz Institute for Catalysis (LIKAT Rostock), Universität Rostock, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
Christopher PenschkeInstitut für Chemie, Universität Potsdam, Karl-Liebknecht Straße 24-25, 14476, Potsdam, Germany.ORCID http://orcid.org/0000-0002-0117-7479
Peter SaalfrankInstitut für Chemie, Universität Potsdam, Karl-Liebknecht Straße 24-25, 14476, Potsdam, Germany.
Bartholomäus PieberDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Arne ThomasDepartment of Chemistry/Functional Materials, Technische Universität Berlin, Hardenbergstraße 40, 10623, Berlin, Germany.ORCID http://orcid.org/0000-0002-2130-4930

Funding

Deutsche Forschungsgemeinschaft BP 1635/2-19Deutsche Forschungsgemeinschaft EXC 2008 - 390540038 - UniSysCat
6 · The paper itself

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.

Indexed as

covalent organic frameworkscross-couplingKeywords: catalysisphotoredoxtuneable activity

Identifiers

PMID36223495
PMCPMC10108091

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.