Evidence map›Paper›PMID 33443314›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2021

Synthetic Approaches to Triarylboranes from 1885 to 2020.

Sarina M Berger, Matthias Ferger, Todd B Marder

Open access · hybridAbstract readReview
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.5field-weighted citation impact, top 2% of its field
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

15 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Host-Guest Doping Enables Room Temperature Phosphorescence from Triarylboranes.Angewandte Chemie (International ed. in English) · 2026
    Article
  3. Diastereoselective Synthesis ofACS catalysis · 2026
    Article
  4. Article
  5. Article
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  13. Synthetic Approaches to Triarylboranes from 1885 to 2020.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Review
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

Sarina M BergerInstitut für Anorganische Chemie and Institute for Sustainable Chemistry, & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0001-8261-7941
Matthias FergerInstitut für Anorganische Chemie and Institute for Sustainable Chemistry, & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0001-9280-0619
Todd B MarderInstitut für Anorganische Chemie and Institute for Sustainable Chemistry, & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.ORCID http://orcid.org/0000-0002-9990-0169
University of Würzburg · DE

Funding

Bayerisches Staatsministerium für Bildung und Kultus, Wissenschaft und Kunst Collaborative Research Network "Solar Technologies go Hybrid"Deutsche Forschungsgemeinschaft GRK 2112Julius-Maximilians-Universität Würzburg
6 · The paper itself

Abstract

In recent years, research in the fields of optoelectronics, anion sensors and bioimaging agents have been greatly influenced by novel compounds containing triarylborane motifs. Such compounds possess an empty p-orbital at boron which results in useful optical and electronic properties. Such a diversity of applications was not expected when the first triarylborane was reported in 1885. Synthetic approaches to triarylboranes underwent various changes over the following century, some of which are still used in the present day, such as the generally applicable routes developed by Krause et al. in 1922, or by Grisdale et al. in 1972 at Eastman Kodak. Some other developments were not pursued further after their initial reports, such as the synthesis of two triarylboranes bearing three different aromatic groups by Mikhailov et al. in 1958. This review summarizes the development of synthetic approaches to triarylboranes from their first report nearly 135 years ago to the present.

Indexed as

arylmetalateboraneschromophoreLewis acidsynthetic methods

Identifiers

PMID33443314
PMCPMC8247992
OpenAlexW3118564699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.