Evidence map›Paper›PMID 29542853›Full record

ReviewChemphyschem : a European journal of chemical physics and physical chemistry2018

Nucleophilic Substitution (S

Trevor A Hamlin, Marcel Swart, F Matthias Bickelhaupt

Abstract readReview
In one paragraph

Review in Chemphyschem : a European journal of chemical physics and physical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing 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

64 citing papers in PubMed.

  1. Article
  2. Article
  3. Leaving-Group Effects in SACS physical chemistry Au · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Understanding the SChemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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.

Trevor A HamlinDepartment of Theoretical Chemistry and, Amsterdam Center for Multiscale Modeling (ACMM), Vrije Universiteit Amsterdam, De Boelelaan 1083, 1081 HV, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-5128-1004
Marcel SwartDepartment of Theoretical Chemistry and, Amsterdam Center for Multiscale Modeling (ACMM), Vrije Universiteit Amsterdam, De Boelelaan 1083, 1081 HV, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-8174-8488
F Matthias BickelhauptDepartment of Theoretical Chemistry and, Amsterdam Center for Multiscale Modeling (ACMM), Vrije Universiteit Amsterdam, De Boelelaan 1083, 1081 HV, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-4655-7747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The reaction potential energy surface (PES), and thus the mechanism of bimolecular nucleophilic substitution (S

Indexed as

bimolecular nucleophilic substitutions (SN2)hypervalencyorganic chemistrypotential energy surfacereaction barriers

Identifiers

PMID29542853
PMCPMC6001448

What OpenQuestion holds

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LicenceCC BY-NC
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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.