Evidence map›Paper›PMID 31484805›Full record

ArticleActa crystallographica. Section C, Structural chemistry2019

The many flavours of halogen bonds - message from experimental electron density and Raman spectroscopy.

Ruimin Wang, Janine George, Shannon Kimberly Potts, Marius Kremer, Richard Dronskowski, Ulli Englert

Abstract read
In one paragraph

Article in Acta crystallographica. Section C, Structural chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Fluxional Halogen Bonds Versus Interlayer Stacking - Theory Meets Experiment.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Halogen-bonded shape memory polymers.Nature communications · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Hydrosulfide (HSAngewandte Chemie (International ed. in English) · 2021
    Article
  10. 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

6 authors.

Ruimin WangInstitute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, Aachen 52056, Germany.
Janine GeorgeInstitute of Condensed Matter and Nanosciences, Chemin des Étoiles 8/L7.03.01, Louvain-la-Neuve 1348, Belgium.ORCID 0000-0001-8907-0336
Shannon Kimberly PottsInstitute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, Aachen 52056, Germany.
Marius KremerInstitute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, Aachen 52056, Germany.
Richard DronskowskiInstitute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, Aachen 52056, Germany.ORCID 0000-0002-1925-9624
Ulli EnglertInstitute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, Aachen 52056, Germany.ORCID 0000-0002-2623-0061

Funding

Deutsche Forschungsgemeinschaft EN309/10, Charge density of halogen bonds and interhalogen contacts
6 · The paper itself

Abstract

Experimental electron-density studies based on high-resolution diffraction experiments allow halogen bonds between heavy halogens to be classified. The topological properties of the electron density in Cl...Cl contacts vary smoothly as a function of the interaction distance. The situation is less straightforward for halogen bonds between iodine and small electronegative nucleophiles, such as nitrogen or oxygen, where the electron density in the bond critical point does not simply increase for shorter distances. The number of successful charge-density studies involving iodine is small, but at least individual examples for three cases have been observed. (a) Very short halogen bonds between electron-rich nucleophiles and heavy halogen atoms resemble three-centre-four-electron bonds, with a rather symmetric heavy halogen and without an appreciable σ hole. (b) For a narrow intermediate range of halogen bonds, the asymmetric electronic situation for the heavy halogen with a pronounced σ hole leads to rather low electron density in the (3,-1) critical point of the halogen bond; the properties of this bond critical point cannot fully describe the nature of the associated interaction. (c) For longer and presumably weaker contacts, the electron density in the halogen bond critical point is only to a minor extent reduced by the presence of the σ hole and hence may be higher than in the aforementioned case. In addition to the electron density and its derived properties, the halogen-carbon bond distance opposite to the σ hole and the Raman frequency for the associated vibration emerge as alternative criteria to gauge the halogen-bond strength. We find exceptionally long C-I distances for tetrafluorodiiodobenzene molecules in cocrystals with short halogen bonds and a significant red shift for their Raman vibrations.

Indexed as

AIM analysiscrystal engineeringcrystal structureexperimental electron densityhalogen bondsRaman spectroscopy

Identifiers

PMID31484805
PMCPMC6727171

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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.