Evidence map›Paper›PMID 41474260›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Substrate-Selective Temperature-Controlled Synthesis of Thiophene Derivatives at Interfaces.

Elena Pérez-Elvira, Ana Barragán, Diego J Vicent, Óscar Jóver, Aurelio Gallardo, Alba García-Frutos, Lenka Černa, Koen Lauwaet, José Santos, Josefina Perles and 7 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

17 authors.

Elena Pérez-Elvira *IMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Ana Barragán *IMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Diego J Vicent *Departamento De Química Orgánica, Facultad De Ciencias Químicas, Universidad Complutense, Madrid, 28040, Spain.
Óscar JóverCNR-Istituto Di Struttura della Materia (CNR-ISM), Roma, 00133, Italy.
Aurelio GallardoIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Alba García-FrutosIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Lenka ČernaIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Koen LauwaetIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
José SantosDepartamento De Química Orgánica, Facultad De Ciencias Químicas, Universidad Complutense, Madrid, 28040, Spain.
Josefina PerlesLaboratorio DRX Monocristal, SIdI, Universidad Autónoma de Madrid, Madrid, 28049, Spain.
José M GallegoInstituto De Ciencia de Materiales de Madrid (ICMM), CSIC, Madrid, 28049, Spain.
Rodolfo MirandaIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
José I UrgelIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
Jonas BjörkMaterials Design Division, Department of Physics, Chemistry and Biology (IFM), Linköping University, Linköping, SE-581 83, Sweden.
Marco Di GiovannantonioCNR-Istituto Di Struttura della Materia (CNR-ISM), Roma, 00133, Italy.ORCID https://orcid.org/0000-0001-8658-9183
Nazario MartínIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.
David ÉcijaIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, 28049, Spain.ORCID https://orcid.org/0000-0002-8661-8295

Funding

Comunidad de MadridItalian Ministry of University and Research (MUR) 2022JW8LHZSpanish State Research Agency (AEI)Swedish Research Council 2022-06725
6 · The paper itself

Abstract

The temperature-controlled transformation of organic molecules at interfaces is an incipient yet powerful strategy for tailoring their structural and physico-chemical properties. In this study, we investigate the substrate- and thermal-selective reactions of bis(3,4-thiophene-fused)tetrabromo-p-benzoquinodimethane molecule (1), focusing on its behavior at distinct coinage metal interfaces, namely Au(111) and Ag(111). Combining scanning probe microscopy and theory, we demonstrate that its sequential transformations are highly dependent on the substrate material and the specific reaction temperatures. When a benzodithiophene precursor, endowed with = CBr

Indexed as

Atomic force microscopyOn‐surface synthesisScanning tunneling microscopyThiophene

Identifiers

PMID41474260
PMCPMC12865235

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.