Evidence map›Paper›PMID 38504923›Full record

ArticleAngewandte Chemie (Weinheim an der Bergstrasse, Germany)2022

Squarephaneic Tetraanhydride: A Conjugated Square-Shaped Cyclophane for the Synthesis of Porous Organic Materials.

Simon Eder, Bowen Ding, Daisy B Thornton, Darlene Sammut, Andrew J P White, Felix Plasser, Ifan E L Stephens, Martin Heeney, Stefano Mezzavilla, Florian Glöcklhofer

Abstract read
In one paragraph

Article in Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 2022. 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
–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

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

10 authors.

Simon EderDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.
Bowen DingDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.
Daisy B ThorntonDepartment of Materials Imperial College London Royal School of Mines London SW7 2AZ UK.ORCID 0000-0001-7011-3834
Darlene SammutDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.
Andrew J P WhiteDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.ORCID 0000-0001-6175-1607
Felix PlasserDepartment of Chemistry Loughborough University Loughborough LE11 3TU UK.ORCID 0000-0003-0751-148X
Ifan E L StephensDepartment of Materials Imperial College London Royal School of Mines London SW7 2AZ UK.ORCID 0000-0003-2157-492X
Martin HeeneyDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.ORCID 0000-0001-6879-5020
Stefano MezzavillaDepartment of Materials Imperial College London Royal School of Mines London SW7 2AZ UK.ORCID 0000-0002-0181-1142
Florian GlöcklhoferDepartment of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.ORCID 0000-0002-6911-8563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aromatic carboxylic anhydrides are ubiquitous building blocks in organic materials chemistry and have received considerable attention in the synthesis of organic semiconductors, pigments, and battery electrode materials. Here we extend the family of aromatic carboxylic anhydrides with a unique new member, a conjugated cyclophane with four anhydride groups. The cyclophane is obtained in a three-step synthesis and can be functionalised efficiently, as shown by the conversion into tetraimides and an octacarboxylate. Crystal structures reveal the high degree of porosity achievable with the new building block. Excellent electrochemical properties and reversible reduction to the tetraanions are shown for the imides; NMR and EPR measurements confirm the global aromaticity of the dianions and evidence the global Baird aromaticity of the tetraanions. Considering the short synthesis and unique properties, we expect widespread use of the new building block in the development of organic materials.

Indexed as

AromaticityCarboxylic AnhydridesConjugated MacrocyclesImidesOrganic Materials

Identifiers

PMID38504923
PMCPMC10947162

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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.