Evidence map›Paper›PMID 41964164›Full record

ArticleAngewandte Chemie (International ed. in English)2026

π-Enlargement in Porphyrin Macrocycles at Interfaces.

Ana Barragán, Elena Pérez-Elvira, Alba García-Frutos, Diego J Vicent, Pingo Mutombo, Koen Lauwaet, José M Gallego, Rodolfo Miranda, José I Urgel, Aurelio Gallardo 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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ana BarragánIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
Elena Pérez-ElviraIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
Alba García-FrutosIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
Diego J VicentDepartamento De Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense, Madrid, Spain.
Pingo MutomboInstitute of Physics of the Czech Academy of Science, Praha, Czech Republic.
Koen LauwaetIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
José M GallegoInstituto De Ciencia de Materiales de Madrid (ICMM), CSIC, Cantoblanco, Madrid, Spain.
Rodolfo MirandaIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
José I UrgelIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
Aurelio GallardoIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
Nazario MartínIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.
David ÉcijaIMDEA Nanoscience, C/ Faraday 9, Campus De Cantoblanco, Madrid, Spain.ORCID https://orcid.org/0000-0002-8661-8295

Funding

Agencia Estatal de Investigacion PID2019-108532GB-I00Agencia Estatal de Investigacion PID2022-136961NB-I0Agencia Estatal de Investigacion PID2023-146373OB-I00Comunidad de Madrid '(MAD2D-CM)-IMDEA-Nanociencia'Comunidad de Madrid '(MAD2D-CM)-UCM'Comunidad de Madrid MOLQUANTUM-CM SYG-2024/TEC-707Comunidad de Madrid QUIMTRONIC-CM Y2018/NMT-4783Comunidad de Madrid SYNMOLMAT-CMComunidad de Madrid TEC-2024/TEC-459European Research Council SyGMagnesis101224406European Research Council SyGTomatto951224Programme for Centers of Excellence in R&D CEX2020-001039-S
6 · The paper itself

Abstract

Porphyrins are essential heteroatomic macrocycles, fundamental to both biological systems and advanced technology. Their unique molecular architecture enables key functions in nature, such as oxygen transport in hemoglobin and light harvesting in chlorophyll, and inspires cutting-edge applications in chemical sensing, catalysis, renewable energy conversion, and optoelectronics. Consequently, significant efforts are dedicated to develop their solution-phase chemistry, particularly by strategically modifying the macrocyclic structure to tailor their properties. Inspired by the field of on-surface covalent synthesis, we introduce a pioneering strategy to tailor porphyrin macrocycles at interfaces, specifically expanding an 18-π porphyrin into a 20-π system. Such transformation is achieved by depositing a porphyrin precursor, equipped with two trifluoromethyl (-CF

Indexed as

antiaromaticityon‐surface synthesisporphyrin chemistryscanning probe microscopy

Identifiers

PMID41964164
PMCPMC13383249

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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.