Evidence map›Paper›PMID 41472412›Full record

ArticleAngewandte Chemie (International ed. in English)2026

A Precisely Bromo-Functionalized [9]Cycloparaphenylene as a Platform for Late-Stage Multisite π-Extension Toward Chiral Nanohoops.

Naoya Kinoshita, Nanami Kotani, Masaya Sugiura, Kotaro Matsumura, Daisuke Sakamaki, Daiki Tauchi, Masashi Hasegawa, Hidetoshi Kawai, Yoshitaka Tsuchido

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

9 authors.

Naoya Kinoshita *Department of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.
Nanami Kotani *Department of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.
Masaya SugiuraDepartment of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.
Kotaro MatsumuraDepartment of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.
Daisuke SakamakiDepartment of Chemistry, Graduate School of Science, Osaka Metropolitan University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka-shi, Osaka, 558-8585, Japan.ORCID https://orcid.org/0000-0001-6503-1607
Daiki TauchiDepartment of Chemistry, Graduate School of Science, Kitasato University, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0373, Japan.ORCID https://orcid.org/0009-0007-5434-2590
Masashi HasegawaDepartment of Chemistry, Graduate School of Science, Kitasato University, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0373, Japan.ORCID https://orcid.org/0000-0003-3302-6496
Hidetoshi KawaiDepartment of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.ORCID https://orcid.org/0000-0002-3367-0153
Yoshitaka TsuchidoDepartment of Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan.ORCID https://orcid.org/0000-0001-8860-0745

Funding

JSPS KAKENHI 20H05866JSPS KAKENHI 21H05496JSPS KAKENHI 21K05093JSPS KAKENHI 23H04041Tokuyama Science Foundation
6 · The paper itself

Abstract

Selective functionalization of [n]cycloparaphenylenes ([n]CPPs) has remained a significant synthetic challenge due to their inherent ring strain. In this study, we present the synthesis of a [9]CPP derivative in which bromo groups are orderly introduced at the 2,5-positions of three benzene rings in the [9]CPP framework, each separated by two phenylene units. The use of our developed Au-mediated CPP synthetic method enabled efficient and scalable access to the target compound in five steps with an overall yield of 37%. The resulting molecule exhibited phosphorescence at low temperature, arising from the heavy-atom effect of the bromo substituents. Furthermore, post-functionalization through Pd-catalyzed coupling reactions demonstrated multisite π-extension and afforded a chiral nanohoop exhibiting exceptional chiroptical performance (|g

Indexed as

Au(I) ComplexCircularly Polarized Luminescence (CPL)CycloparaphenylenePhosphorescenceπ‐Extension

Identifiers

PMID41472412
PMCPMC12865238

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.