Size and Polarizability as Design Principles for Stereoselective Catalysis

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.

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Publication Details

Journal
Chemistry - A European Journal
Published
2025-11-02
DOI
https://doi.org/10.1002/chem.202502741
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Size and Polarizability as Design Principles for Stereoselective Catalysis

Caroline M. Carter, Hendrik Zipse, Jan Brossette
Chemistry - A European Journal
Synthesis and Properties of Aromatic Compounds
article

Size and Polarizability as Design Principles for Stereoselective Catalysis

Caroline M. Carter, Hendrik Zipse, Jan Brossette
article en

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.

Chemistry - A European JournalVol. 31(68)
LMU Klinikum (DE), Ludwig-Maximilians-Universität München (DE)
Deutsche Forschungsgemeinschaft, Leibniz-Gemeinschaft, Leibniz-Rechenzentrum
Openalex Percentile: Top 75%
Synthesis and Properties of Aromatic Compounds
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