Journalartikel

Attraction or Repulsion? London Dispersion Forces Control Azobenzene Switches


AutorenlisteSchweighauser, L; Strauss, MA; Bellotto, S; Wegner, HA

Jahr der Veröffentlichung2015

Seiten13436-13439

ZeitschriftAngewandte Chemie International Edition

Bandnummer54

Heftnummer45

ISSN1433-7851

DOI Linkhttps://doi.org/10.1002/anie.201506126

VerlagWiley


Abstract
Large substituents are commonly seen as entirely repulsive through steric hindrance. Such groups have additional attractive effects arising from weak London dispersion forces between the neutral atoms. Steric interactions are recognized to have a strong influence on isomerization processes, such as in azobenzene-based molecular switches. Textbooks indicate that steric hindrance destabilizes the Zisomers. Herein, we demonstrate that increasing the bulkiness of electronically equal substituents in the meta-position decreases the thermal reaction rates from the Z to the E isomers. DFT computations revealed that attractive dispersion forces essentially lower the energy of the Z isomers.



Zitierstile

Harvard-ZitierstilSchweighauser, L., Strauss, M., Bellotto, S. and Wegner, H. (2015) Attraction or Repulsion? London Dispersion Forces Control Azobenzene Switches, Angewandte Chemie International Edition, 54(45), pp. 13436-13439. https://doi.org/10.1002/anie.201506126

APA-ZitierstilSchweighauser, L., Strauss, M., Bellotto, S., & Wegner, H. (2015). Attraction or Repulsion? London Dispersion Forces Control Azobenzene Switches. Angewandte Chemie International Edition. 54(45), 13436-13439. https://doi.org/10.1002/anie.201506126



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