Evidence map›Paper›PMID 40767509›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Poly(p-phenylene phosphaborene): A Modified Poly(p-phenylene vinylene) with π-Conjugated B═P Linkages.

Julian Glock, Jonas Klopf, Merian Crumbach, Johannes Chorbacher, Johannes S Schneider, Alexandra Friedrich, Emilia Buchsteiner, Tobias Bischof, Maik Finze, Bernd Engels and 1 more

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Conjugated Inorganic-Organic Hybrid Polymers with p-Block Elements.Angewandte Chemie (International ed. in English) · 2026
    Review
  3. 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

11 authors.

Julian GlockInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Jonas KlopfInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Merian CrumbachInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Johannes ChorbacherInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Johannes S SchneiderInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Alexandra FriedrichInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.ORCID https://orcid.org/0000-0002-1411-7336
Emilia BuchsteinerRigaku Europe SE, Hugenottenallee 167, 63263, Neu-Isenburg, Germany.ORCID https://orcid.org/0000-0001-7599-305X
Tobias BischofInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Maik FinzeInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Bernd EngelsInstitute of Physical and Theoretical Chemistry, Julius-Maximilians-Universität Würzburg, Emil-Fischer-Str. 42, 97074, Würzburg, Germany.
Holger HeltenInstitute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB), Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.

Funding

Deutsche Forschungsgemeinschaft 401739196Deutsche Forschungsgemeinschaft 466754611Deutsche Forschungsgemeinschaft 468457264Deutsche Forschungsgemeinschaft HE 6171/6-2Deutsche Forschungsgemeinschaft HE 6171/9-1
6 · The paper itself

Abstract

While the isoelectronic substitution of selected C═C by B═N units in π-conjugated organic compounds has evolved into a well-established concept to create novel hybrid materials with modified properties, the use of valence isoelectronic B═P units for such purposes has been hardly explored. Herein, we demonstrate substitutional doping of the famous optoelectronic organic polymer poly(p-phenylene vinylene) (PPV) with B═P linking groups for the first time. We report on the successful synthesis of a soluble polymer and a series of monodisperse oligomers of BP-PPV type. Our structural and photophysical investigations, supported by in-depth DFT calculations, evidence effective π-conjugation along their backbone, which is similary pronounced as in their previously reported BN congeners. In addition, the novel BCP compounds show distinct fluorescence emission in solution and emission enhancement upon aggregation (AIEE), occurring from a P-pyramidalized excited state.

Indexed as

BP compoundsConjugated polymersHybrid polymersPhosphinoboranesPoly(p‐phenylene vinylene)

Identifiers

PMID40767509
PMCPMC12435409

What OpenQuestion holds

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LicenceCC BY
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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.