Evidence map›Paper›PMID 41994953›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Stable Synapse-Like Memory Switching in N-Heterocyclic Carbene Monolayers.

Ankita Das, Alessandro Borrini, Christian Gutheil, Björn Braunschweig, Billura Shakhayeva, Georgios Katsoukis, Ab F Nieuwenhuis, Raka Ahmed, Susanne Leitherer, Gemma C Solomon and 2 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Ankita DasOrganisch-Chemisches Institut, University of Münster, Münster, Germany.
Alessandro BorriniHybrid Materials for Opto-Electronics Group, Department of Molecules and Materials, MESA+ Institute for Nanotechnology, Molecules Center and Center for Brain-Inspired Nano Systems, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.
Christian GutheilOrganisch-Chemisches Institut, University of Münster, Münster, Germany.
Björn BraunschweigInstitute of Physical Chemistry, University of Münster, Münster, Germany.
Billura ShakhayevaInstitute of Physical Chemistry, University of Münster, Münster, Germany.
Georgios KatsoukisCatalytic Processes & Materials Group, Department of Chemical Engineering, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.
Ab F NieuwenhuisHybrid Materials for Opto-Electronics Group, Department of Molecules and Materials, MESA+ Institute for Nanotechnology, Molecules Center and Center for Brain-Inspired Nano Systems, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.
Raka AhmedDepartment of Chemistry and Nano-Science Center, University of Copenhagen, Copenhagen Ø, Denmark.
Susanne LeithererDepartment of Chemistry and Nano-Science Center, University of Copenhagen, Copenhagen Ø, Denmark.
Gemma C SolomonDepartment of Chemistry and Nano-Science Center, University of Copenhagen, Copenhagen Ø, Denmark.
Frank GloriusOrganisch-Chemisches Institut, University of Münster, Münster, Germany.ORCID https://orcid.org/0000-0002-0648-956X
Christian A NijhuisHybrid Materials for Opto-Electronics Group, Department of Molecules and Materials, MESA+ Institute for Nanotechnology, Molecules Center and Center for Brain-Inspired Nano Systems, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.

Funding

Deutsche Forschungsgemeinschaft 951519European Research Council 865870Ministry for Culture and Science of North Rhine Westphalia, Germany (International Graduate School for Battery Chemistry, Characterization, Analysis, Recycling and Application (BACCARA)Novo Nordisk Foundation NNF210C0071282
6 · The paper itself

Abstract

We report a robust redox-active N-heterocyclic carbene (NHC) monolayer that exhibits synapse-like behavior driven by proton-coupled electron transfer (PCET). Our quinone-functionalized NHC (Rex-NHC) forms densely packed, upright self-assembled monolayers (SAMs) on Au, confirmed by cyclic voltammetry, x- ray photoelectron spectroscopy, sum-frequency generation spectroscopy, and infrared reflection absorption spectroscopy. Molecular junctions built as Au-Rex-NHC//Ga

Identifiers

PMID41994953
PMCPMC13266966

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.