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http://dx.doi.org/10.5012/bkcs.2006.27.4.508

Ab initio Study of the Complexes of Trimethyl Ether of Monodeoxycalix[4]arene with Potassium Ion: Cation-π Interactions  

Lee, Hyung-Dae (Department of Chemistry, Chung-Ang University)
Kim, Kwang-Ho (Department of Chemistry, Chung-Ang University)
Lee, Ho-Jun (Department of Chemistry, Chung-Ang University)
Lee, Sik (Center for Computational Biology and Bioinformatics, Korea Institute of Science and Technology Information)
Nanbu, Shinkoh (Computing and Communications Center, Kyushu University)
Choe, Jong-In (Department of Chemistry, Chung-Ang University)
Publication Information
Bulletin of the Korean Chemical Society / v.27, no.4, 2006 , pp. 508-514 More about this Journal
Abstract
In this study, we have performed ab initio computer simulations to investigate the conformational and complexation characteristics of the trimethyl ether of p-tert-butylmonodeoxycalix[4]arene (6) with a potassium ion. The structures of different conformers of 6 and their potassium complexes were optimized by using ab initio RHF/6-31G and B3LYP/6-31G(d,p) methods. The relative stability of the various conformers of the uncomplexed 6 is in following order: cone (most stable) > 1-partial-cone ~ 2i-partial-cone > 2-partial-cone ~ 1,3-alternate > 3i-partial-cone. However, the relative stability of the conformational complexes of 6 with $K^+$ is in the following order: 2-partial cone ~ 1,3-alternate > cone > 3-partial cone > 1-partial cone (least stable). The highest binding strengths of 2-partial-cone and 1,3-alternate complexes originate from two strong cation-$\pi$ interactions and two strong cation-oxygen interactions in the complex of 6+$K^+$. Due to the cation-$\pi$ interactions, the calculated C-C bond distances in the arenes of the $K^+$-complexes are about 0.0048 $\AA$ longer than the values of their isolated hosts.
Keywords
Ab initio; B3LYP/6-31G; Monodeoxycalix[4]arene; Conformer; Cation-$\pi$ interaction;
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Times Cited By Web Of Science : 3  (Related Records In Web of Science)
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