Journalartikel
Autorenliste: Rummel, Lars; Schreiner, Peter R.
Jahr der Veröffentlichung: 2024
Zeitschrift: Angewandte Chemie International Edition
Bandnummer: 63
Heftnummer: 12
ISSN: 1433-7851
eISSN: 1521-3773
Open Access Status: Hybrid
DOI Link: https://doi.org/10.1002/anie.202316364
Verlag: Wiley
London dispersion (LD) interactions are the main contribution of the attractive part of the van der Waals potential. Even though LD effects are the driving force for molecular aggregation and recognition, the role of these omnipresent interactions in structure and reactivity had been largely underappreciated over decades. However, in the recent years considerable efforts have been made to thoroughly study LD interactions and their potential as a chemical design element for structures and catalysis. This was made possible through a fruitful interplay of theory and experiment. This review highlights recent results and advances in utilizing LD interactions as a structural motif to understand and utilize intra- and intermolecularly LD-stabilized systems. Additionally, we focus on the quantification of LD interactions and their fundamental role in chemical reactions. It has by now been realized that London dispersion (LD) interactions, the main contributor to the attractive part of the van der Waals potential, are ubiquitously present and need to be taken into consideration in structures and dynamics of chemical reactions. This review highlights recent experimental and theoretical advances in utilizing LD interactions as a design element. image
Abstract:
Zitierstile
Harvard-Zitierstil: Rummel, L. and Schreiner, P. (2024) Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry, Angewandte Chemie International Edition, 63(12). https://doi.org/10.1002/anie.202316364
APA-Zitierstil: Rummel, L., & Schreiner, P. (2024). Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry. Angewandte Chemie International Edition. 63(12). https://doi.org/10.1002/anie.202316364
Schlagwörter
ATTRACTIVE NONCOVALENT INTERACTIONS; CENTRAL BOND-LENGTH; DENSITY-FUNCTIONAL THEORY; DIPHENYL ETHER-METHANOL; ENANTIOSELECTIVE ACYL TRANSFER; STERIC ATTRACTION; Structure and Reactivity