Evidence map›Paper›PMID 32286829›Full record

ArticleJournal of the American Chemical Society2020

Hypervalent Iodine(III) Compounds as Biaxial Halogen Bond Donors.

Flemming Heinen, Elric Engelage, Christopher J Cramer, Stefan M Huber

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Probing Weak Halogen Bonding in Aqueous Solution.Journal of the American Chemical Society · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cyclic Homo- and Heterohalogen Di-λJournal of the American Chemical Society · 2023
    Article
  11. Review
  12. Chiral Bromonium Salt (Hypervalent Bromine(III)) withMolecules (Basel, Switzerland) · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. A Bidentate Iodine(III)-Based Halogen-Bond Donor as a Powerful Organocatalyst*.Angewandte Chemie (International ed. in English) · 2021
    Article
  19. Article
  20. Comparison of Bifurcated Halogen with Hydrogen Bonds.Molecules (Basel, Switzerland) · 2021
    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

4 authors.

Flemming HeinenFakultät für Chemie und Biochemie, Organische Chemie I, Ruhr-Universität Bochum, Universitätsstraße 150,44801 Bochum, Germany.
Elric EngelageFakultät für Chemie und Biochemie, Organische Chemie I, Ruhr-Universität Bochum, Universitätsstraße 150,44801 Bochum, Germany.
Christopher J CramerDepartment of Chemistry, Chemical Theory Center, and Minnesota Supercomputing Institute, University of Minnesota, 207 Pleasant Street SE, Minneapolis 55455-0431, Minnesota, United States.ORCID http://orcid.org/0000-0001-5048-1859
Stefan M HuberFakultät für Chemie und Biochemie, Organische Chemie I, Ruhr-Universität Bochum, Universitätsstraße 150,44801 Bochum, Germany.ORCID http://orcid.org/0000-0002-4125-159X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

"Hypervalent" iodine(III) derivatives have been established as powerful reagents in organic transformations, but so far only a handful of studies have addressed their potential use as halogen-bonding noncovalent Lewis acids. In contrast to "classical" halogen-bond donors based on iodine(I) compounds, iodine(III) salts feature two directional electrophilic axes perpendicular to each other. Herein we present the first systematic investigation on biaxial binding to such Lewis acids in solution. To this end, hindered and unhindered iodolium species were titrated with various substrates, including diesters and diamides, via

Identifiers

PMID32286829
PMCPMC7252947

What OpenQuestion holds

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Registered trials

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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.