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.
Authors
- Caroline M. Carter (ORCID: https://orcid.org/0009-0004-0557-5994)
- Hendrik Zipse (ORCID: https://orcid.org/0000-0002-0534-3585)
- Jan Brossette (ORCID: https://orcid.org/0000-0002-7179-048X)
Institutions
- LMU Klinikum (DE)
- Ludwig-Maximilians-Universität München (DE)
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
Funders
- Deutsche Forschungsgemeinschaft
- Leibniz-Gemeinschaft
- Leibniz-Rechenzentrum