| Literature DB >> 26350759 |
Luca Schweighauser1, Marcel A Strauss1, Silvia Bellotto1, Hermann A Wegner2.
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 Z isomers. 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.Entities:
Keywords: London dispersion; azobenzene; isomerization; molecular switches; steric interactions
Year: 2015 PMID: 26350759 DOI: 10.1002/anie.201506126
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336