Evidence map›Paper›PMID 33112494›Full record

ArticleAngewandte Chemie (International ed. in English)2021

One-Pot Synthesis of Boron-Doped Polycyclic Aromatic Hydrocarbons via 1,4-Boron Migration.

Jin-Jiang Zhang, Man-Chung Tang, Yubin Fu, Kam-Hung Low, Ji Ma, Lin Yang, Jan J Weigand, Junzhi Liu, Vivian Wing-Wah Yam, Xinliang Feng

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Metal-Free Electrophilic Borylative Cyclizations of Alkynes.Chemical record (New York, N.Y.) · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Regio- and Stereoselective 1,2-Carboboration of Ynamides with Aryldichloroboranes.Angewandte Chemie (International ed. in English) · 2021
    Article
  11. 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

10 authors.

Jin-Jiang ZhangCenter for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.
Man-Chung TangInstitute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Rokfulam Road, Hong Kong, P. R. China.
Yubin FuCenter for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.
Kam-Hung LowInstitute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Rokfulam Road, Hong Kong, P. R. China.
Ji MaCenter for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.ORCID http://orcid.org/0000-0003-4418-2339
Lin YangCenter for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.
Jan J WeigandChair of Inorganic Molecular Chemistry & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.
Junzhi LiuInstitute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Rokfulam Road, Hong Kong, P. R. China.
Vivian Wing-Wah YamInstitute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Rokfulam Road, Hong Kong, P. R. China.
Xinliang FengCenter for Advancing Electronics Dresden (cfaed) & Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062, Dresden, Germany.ORCID http://orcid.org/0000-0003-3885-2703

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we demonstrate a novel one-pot synthetic method towards a series of boron-doped polycyclic aromatic hydrocarbons (B-PAHs, 1 a-1 o), including hitherto unknown B-doped zethrene derivatives, from ortho-aryl substituted diarylalkynes with high atom efficiency and broad substrate scopes. A reaction mechanism is proposed based on the experimental investigation together with the theoretical calculations, which involves a unique 1,4-boron migration process. The resultant benchtop-stable B-PAHs are thoroughly investigated by X-ray crystallography, cyclic voltammetry, UV/Vis absorption, and fluorescence spectroscopies. The blue and green organic light-emitting diode (OLED) devices based on 1 f and 1 k are further fabricated, demonstrating the promising application potential of B-PAHs in organic optoelectronics.

Indexed as

1,4-boron migrationboron dopingnanographenesorganic electronicspolycyclic aromatic hydrocarbons (PAHs)

Identifiers

PMID33112494
PMCPMC7898796

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.