Evidence map›Paper›PMID 42813015›Full record

ArticleChemical science2026

Cross-dehydrogenative coupling macrocyclization for the construction of donor-acceptor nanohoops.

Baitan Chakraborty, Yury Torubaev, Yuan-Qiu-Qiang Yi, Naoki Nakatani, Christine K Luscombe

Abstract read
In one paragraph

Article in Chemical science, 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

5 authors.

Baitan ChakrabortyPi-Conjugated Polymers Unit, Okinawa Institute of Science and Technology Graduate University Okinawa 904-0495 Japan christine.luscombe@oist.jp.ORCID https://orcid.org/0000-0002-9853-0151
Yury TorubaevNanofabrication Section, Core Facilities, Okinawa Institute of Science and Technology Graduate University Okinawa 904-0495 Japan.ORCID https://orcid.org/0000-0002-7835-0591
Yuan-Qiu-Qiang YiPi-Conjugated Polymers Unit, Okinawa Institute of Science and Technology Graduate University Okinawa 904-0495 Japan christine.luscombe@oist.jp.ORCID https://orcid.org/0000-0003-3522-7056
Naoki NakataniDepartment of Chemistry, Graduate School of Science and Engineering, Tokyo Metropolitan University Hachioji Tokyo 192-0397 Japan.ORCID https://orcid.org/0000-0002-9100-137X
Christine K LuscombePi-Conjugated Polymers Unit, Okinawa Institute of Science and Technology Graduate University Okinawa 904-0495 Japan christine.luscombe@oist.jp.ORCID https://orcid.org/0000-0001-7456-1343

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor (D) and acceptor (A) (D-A) architectures in cycloparaphenylenes (CPPs), or nanohoops, offer property tunability beyond what can be controlled by ring size. However, the synthesis of D-A nanohoops using traditional cross-coupling requires monomer prefunctionalization, which reduces step and atom economy. We report a catalytic cross-dehydrogenative coupling (CDC) macrocyclization strategy to access the [8]nanohoop cyclo(2,5-thienylene)(perfluoro-1,4-phenylene) ([8]CTPFP) with D-A architecture. A strain-relieving L-shaped precursor bearing thiophene termini is used in a Pd-catalyzed C-H/C-H cross-coupling reaction with 1,2,4,5-tetrafluorobenzene to form the precursor macrocycle pre[8]CTPFP in an atom- and step-economic route, circumventing the use of organometallic reagents. Subsequently, a BBr

Identifiers

PMID42813015
PMCPMC13621426

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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.