Evidence map›Paper›PMID 37824606›Full record

ArticleScience advances2023

Electric field-assisted anion-π catalysis on carbon nanotubes in electrochemical microfluidic devices.

M Ángeles Gutiérrez López, Rojan Ali, Mei-Ling Tan, Naomi Sakai, Thomas Wirth, Stefan Matile

Abstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Organocatalytic Microfluidic Double-Layer Capacitors.Angewandte Chemie (International ed. in English) · 2025
    Article
  8. Oriented Electric Fields─Universal Catalysts.Accounts of chemical research · 2025
    Article
  9. Article
  10. Review
  11. Anion-π catalysis on carbon allotropes.Beilstein journal of organic chemistry · 2023
    Review
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

6 authors.

M Ángeles Gutiérrez LópezDepartment of Organic Chemistry, University of Geneva, Quai Ernest Ansermet 30, CH-1211 Geneva 4, Switzerland.ORCID 0009-0007-4606-8392
Rojan AliSchool of Chemistry, Cardiff University, Park Place, Main Building, Cardiff CF10 3AT, UK.ORCID 0009-0001-3861-0045
Mei-Ling TanDepartment of Organic Chemistry, University of Geneva, Quai Ernest Ansermet 30, CH-1211 Geneva 4, Switzerland.ORCID 0000-0001-7983-3432
Naomi SakaiDepartment of Organic Chemistry, University of Geneva, Quai Ernest Ansermet 30, CH-1211 Geneva 4, Switzerland.ORCID 0000-0002-9460-1944
Thomas WirthSchool of Chemistry, Cardiff University, Park Place, Main Building, Cardiff CF10 3AT, UK.ORCID 0000-0002-8990-0667
Stefan MatileDepartment of Organic Chemistry, University of Geneva, Quai Ernest Ansermet 30, CH-1211 Geneva 4, Switzerland.ORCID 0000-0002-8537-8349

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vision to control the charges migrating during reactions with external electric fields is attractive because of the promise of general catalysis, emergent properties, and programmable devices. Here, we explore this idea with anion-π catalysis, that is the stabilization of anionic transition states on aromatic surfaces. Catalyst activation by polarization of the aromatic system is most effective. This polarization is induced by electric fields. The use of electrochemical microfluidic reactors to polarize multiwalled carbon nanotubes as anion-π catalysts emerges as essential. These reactors provide access to high fields at low enough voltage to prevent electron transfer, afford meaningful effective catalyst/substrate ratios, and avoid interference from additional electrolytes. Under these conditions, the rate of pyrene-interfaced epoxide-opening ether cyclizations is linearly voltage-dependent at positive voltages and negligible at negative voltages. While electromicrofluidics have been conceived for redox chemistry, our results indicate that their use for supramolecular organocatalysis has the potential to noncovalently electrify organic synthesis in the broadest sense.

Identifiers

PMID37824606
PMCPMC10569703

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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.