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A DFT study of the complexation behavior of hemispherands toward alkali metal cations
Author(s) -
Shibl Mohamed F.,
Hameed Salem A.,
Elroby Shabaan A.K.
Publication year - 2010
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.22505
Subject(s) - alkali metal , ionic radius , chemistry , binding energy , density functional theory , ionic bonding , ion , metal , computational chemistry , ligand (biochemistry) , group (periodic table) , inorganic chemistry , metal ions in aqueous solution , crystallography , atomic physics , organic chemistry , physics , biochemistry , receptor
A density functional theory study of the behavior of hemispherands toward alkali metal ions (Li + , Na + , and K + ) is performed. The effect of the replacement of the rigid anisyl group(s) by the mobile ether group(s) on the binding energy of hemispherands with alkali metal ions is investigated. The results indicated that the binding energies are inversely proportional to the ionic radius of the cations. Moreover, increasing the flexibility of the ligand results in decreasing the binding toward small ions. The structures of the hosts and the guests are correlated to the binding energies, and the correlations are interpreted in terms of the principle of preorganization. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem, 2010