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HERO ID
4285276
Reference Type
Journal Article
Title
sigma-sigma, sigma-pi, and pi-pi Stacking Interactions between Six-Membered Cyclic Systems. Dispersion Dominates and Electrostatics Commands
Author(s)
Cabaleiro-Lago, EM; Rodriguez-Otero, J
Year
2017
Journal
ChemistrySelect
ISSN:
2365-6549
Volume
2
Issue
18
Page Numbers
5157-5166
Language
English
DOI
10.1002/slct.201700671
Web of Science Id
WOS:000406674900024
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85041698193&doi=10.1002%2fslct.201700671&partnerID=40&md5=106dd7ea478f2a8a766edd5493e3e548
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Abstract
The characteristics of the interaction in aliphatic-aliphatic (sigma-sigma), aliphatic-aromatic (sigma-pi), and aromatic-aromatic (pi-pi) dimers have been studied employing benzene, cyclohexane and some of their fluorinated derivatives. Though fluorination dramatically changes the electrostatic properties of the molecules, the interaction only changes notably when the fluorinated species interacts with a significantly polar molecule. Fluorination hardly affects the interaction with cyclohexane or trifluorobenzene, both with small dipole and quadrupole moments. The results indicate that whereas dispersion constitutes the leading stabilising contribution in most of the dimers considered, it is the electrostatic term the one reflecting the changes on the interaction introduced by fluorination. As a consequence, the order of stability of the complexes studied follows the trends observed for the electrostatic term, despite not being the largest stabilising contribution.
Keywords
computational chemistry; noncovalent interactions; pi interactions; stacking interactions; CH-pi contacts
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