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Study on the Cation‐π Interactions between Ammonium Ion and Aromatic π Systems
Author(s) -
Wang ZhaoXu,
Zhang JingChang,
Cao WeiLiang
Publication year - 2006
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.200690287
Subject(s) - chemistry , substituent , interaction energy , chemical physics , aromaticity , computational chemistry , london dispersion force , toluene , dispersion (optics) , ammonium , ion , decomposition , critical point (mathematics) , stereochemistry , organic chemistry , molecule , quantum mechanics , van der waals force , physics , mathematical analysis , mathematics
The nature and strength of the cation‐π interactions betweenand toluene, p ‐cresol, or Me‐indole were studied in terms of the topological properties of molecular charge density and binding energy decomposition. The results display that the diversity in the distribution pattern of bond and cage critical points reflects the profound influence of the number and nature of substituent on the electron density of the aromatic rings. On the other hand, the energy decomposition shows that dispersion and repulsive exchange forces play an important role in the organic cation ()‐π interaction, although the electrostatic and induction forces dominate the interaction. In addition, it is intriguing that there is an excellent correlation between the electrostatic energy and ellipticity at the bond critical point of the aromatic π systems, which would be helpful to further understand the electrostatic interaction in the cation‐π complexes.