Evidence map›Paper›PMID 39655504›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Metal-Bridging Cyclic Bilatriene Analogue Affords Stable π-Radicaloid Dyes with Near-Infrared II Absorption.

Aninda Ghosh, Shigeki Mori, Yuki Ide, Jun Tae Song, Yoshihisa Yamaoka, Tatsumi Ishihara, Takahisa Ikeue, Hiroyuki Furuta, Masatoshi Ishida

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

9 authors.

Aninda GhoshDepartment of Chemistry, Graduate School of Sciences, Tokyo Metropolitan University, Hachioji, 192-0397, Japan.
Shigeki MoriAdvanced Research Support Center, Ehime University, Matsuyama, 790-8577, Japan.ORCID https://orcid.org/0000-0001-6731-2357
Yuki IdeInstitute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo, 001-0021, Japan.ORCID https://orcid.org/0000-0003-0648-0503
Jun Tae SongDepartment of Applied Chemistry, Graduate School of Engineering, and International Institute for Carbon Neutral Energy Research (I2CNER), Kyushu University, Fukuoka, 819-0395, Japan.ORCID https://orcid.org/0000-0003-1047-6152
Yoshihisa YamaokaFaculty of Health Sciences, Department of Clinical Engineering, Komatsu University, Komatsu, 923-0961, Japan.ORCID https://orcid.org/0000-0001-6395-7721
Tatsumi IshiharaDepartment of Applied Chemistry, Graduate School of Engineering, and International Institute for Carbon Neutral Energy Research (I2CNER), Kyushu University, Fukuoka, 819-0395, Japan.ORCID https://orcid.org/0000-0002-7434-3773
Takahisa IkeueDepartment of Chemistry, Interdisciplinary Graduate School of Science and Engineering, Shimane University, Matsue, 690-8504, Japan.ORCID https://orcid.org/0000-0002-1673-1532
Hiroyuki FurutaDepartment of Applied Chemistry, Graduate School of Engineering, and International Institute for Carbon Neutral Energy Research (I2CNER), Kyushu University, Fukuoka, 819-0395, Japan.ORCID https://orcid.org/0000-0002-3881-8807
Masatoshi IshidaDepartment of Chemistry, Graduate School of Sciences, Tokyo Metropolitan University, Hachioji, 192-0397, Japan.ORCID https://orcid.org/0000-0002-1117-2188

Funding

Izumi Science and Technology FoundationJapan Science and Technology Corporation JPMJPR2103Japan Society for the Promotion of Science London JP20H00406Japan Society for the Promotion of Science London JP22K19937
6 · The paper itself

Abstract

Stable neutral metal radicaloid complexes have been synthesized from a modified tetrapyrrolic pigment, bilatriene, with iridium(I) and rhodium(I) cyclooctadiene (COD) synthons. The bilatriene skeleton contains α-linked conjugated pyrrole units, whereas an N-confused analogue used in this work possesses β-linked pyrrole moieties at the terminal, demonstrating a unique metal binding capability. Unprecedentedly, the metal-COD cations are accommodated at the outer nitrogen sites, which induced the formation of open-shell metal-radicaloid species. The resulting compounds are highly stable under ambient conditions and demonstrated facile redox conversion to afford the corresponding cation and anion species. Furthermore, the radicaloid complexes showed a distinct second near-infrared absorption (NIR-II) capability extending up to 1500 nm along with high photostability. These features emphasized that the complexes can be potential NIR-II light-responsible photothermal and photoacoustic imaging contrast agents based on the metal-radicaloid dye platform.

Indexed as

metal coordinationnear-infrared lightphotoacousticporphyrinoidradical

Identifiers

PMID39655504
PMCPMC11795725

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Registered trials

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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.