Dispersion Interactions in Condensed Phases and inside Molecular Containers
Author:
Affiliation:
1. Al-Balqa Applied University, Faculty of Science, Department of Chemistry, 19117 Al-Salt, Jordan
2. Constructor University, School of Science, Campus Ring 1, 28759 Bremen, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.3c00523
Reference75 articles.
1. Polarizabilities Inside Molecular Containers This work was supported by the Swiss National Science Foundation (projects 620-58000.99 and 4047-057552) within the program NFP 47 “Supramolecular Functional Materials”.
2. HYDROPHOBE Challenge: A Joint Experimental and Computational Study on the Host–Guest Binding of Hydrocarbons to Cucurbiturils, Allowing Explicit Evaluation of Guest Hydration Free-Energy Contributions
3. Cavitation energies can outperform dispersion interactions
4. Preferential binding of unsaturated hydrocarbons in aryl-bisimidazolium·cucurbit[8]uril complexes furbishes evidence for small-molecule π–π interactions
5. Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces
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1. Distinction and Quantification of Noncovalent Dispersive and Hydrophobic Effects;Molecules;2024-04-02
2. Single-Molecule Exchange inside a Nanocage Provides Insights into the Origin of π–π Interactions;Journal of the American Chemical Society;2024-03-27
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