Evidence map›Paper›PMID 41178212›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2025

Size and Polarizability as Design Principles for Stereoselective Catalysis.

Caroline M Carter, Jan Brossette, Hendrik Zipse

Abstract readReview
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Assessing Benzene Dimer Interactions in Solution With a Molecular Balance.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    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.

Caroline M CarterDepartment of Chemistry, LMU Munich, Butenandtstraße 5-13, 81377, Munich, Germany.ORCID https://orcid.org/0009-0004-0557-5994
Jan BrossetteDepartment of Chemistry, LMU Munich, Butenandtstraße 5-13, 81377, Munich, Germany.ORCID https://orcid.org/0000-0002-7179-048X
Hendrik ZipseDepartment of Chemistry, LMU Munich, Butenandtstraße 5-13, 81377, Munich, Germany.ORCID https://orcid.org/0000-0002-0534-3585

Funding

Deutsche Forschungsgemeinschaft, 426795949
6 · The paper itself

Abstract

Molecular volumes and isotropic polarizabilities of a larger number of carbocyclic π-systems ranging from benzene on the small to heptacene on the large end are provided in order to facilitate the analysis of positively size-dependent catalytic processes, where an increase in substrate or catalyst size leads to an increase in reaction rate and/or reaction stereoselectivity. The utility of this approach is demonstrated for selected stereoselective catalytic processes from the contemporary literature.

Indexed as

isotropic polarizabilityLondon dispersion forcesmolecular volumenoncovalent interactionsstereoselective catalysis

Identifiers

PMID41178212
PMCPMC12679343

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.