Evidence map›Paper›PMID 41194420›Full record

ArticleThe journal of physical chemistry letters2025

On-Surface Synthesis of Azobenzene-Linked Porphyrin Derivatives.

Yuji Isshiki, Donglin Li, Saranyan Vijayaraghavan, Kewei Sun, Huynh Thien Ngo, Luiza Buimaga-Iarinca, Yoshitaka Matsushita, Edward A Neal, Cristian Morari, Jonathan P Hill and 1 more

Abstract read
In one paragraph

Article in The journal of physical chemistry letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

11 authors.

Yuji IsshikiCenter for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.
Donglin LiCenter for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.
Saranyan VijayaraghavanCSIR-Central Electrochemical Research Institute, Karaikudi 630003, India.
Kewei SunCenter for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.ORCID 0000-0002-1835-243X
Huynh Thien NgoResearch Center for Materials Nanoarchitectonics, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Luiza Buimaga-IarincaNational Institute for Research and Development of Isotopic and Molecular Technologies (NIRDIMT), 65-103 Donat, 400293 Cluj-Napoca, Romania.
Yoshitaka MatsushitaResearch Network and Facility Services Division, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.ORCID 0000-0002-4968-8905
Edward A NealResearch Center for Materials Nanoarchitectonics, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.ORCID 0000-0002-5464-9097
Cristian MorariNational Institute for Research and Development of Isotopic and Molecular Technologies (NIRDIMT), 65-103 Donat, 400293 Cluj-Napoca, Romania.ORCID 0000-0003-1989-3278
Jonathan P HillResearch Center for Materials Nanoarchitectonics, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.ORCID 0000-0002-4229-5842
Shigeki KawaiCenter for Basic Research on Materials, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan.ORCID 0000-0003-2128-0120

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

On-surface synthesis has become an attractive strategy to obtain functionalized carbon nanostructures from small precursor molecules using a bottom-up approach. Although various on-surface reactions have been developed, it is still unclear how the chirality of self-assembled structures prior to reaction affects the coupling process. Here, we investigate homocoupling of nitro-phenyl groups in Pt-porphyrin derivatives on Au(111) surfaces using low-temperature scanning tunneling microscopy. Two different self-assembled structures composed either of linear oligomer of molecules of opposing chirality or of discrete trimers of molecules having the same chirality (i.e., homochiral) were respectively obtained by using differently substituted phenyl and 3,5-di-

Identifiers

PMID41194420
PMCPMC12621240

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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.