4.6 Article

Dynamic NMR Study of the Kinetics of Complexation of TI+ Ion with Calix[4]crown-6

Journal

JOURNAL OF PHYSICAL CHEMISTRY A
Volume 114, Issue 28, Pages 7462-7469

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp101662f

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Funding

  1. Tarbiat Modares University Research Council

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The complexation and exchange kinetics and mechanism for the dissociation and conformational change of thallium ion complex of calix[4]crown-6 were studied in CD3CN/CDCl3 (4:1 v/v) solution by dynamic H-1 NMR. The results show the formation of a 1:1 complex with cone conformation. From variable temperature dynamic NMR analysis in the range 223-293 K, two coalescence temperatures at 228 and 243 K were ascertained. The activation parameters for the dissociation process, E-a (kJ/mol), Delta S-double dagger (J/mol.K), and Delta H-double dagger (kJ/mol) are 11.0, -133.2, and 10.1 for the bimolecular regime and 21.5, -112.8, and 20.6 for the unimolecular regime, respectively. In addition, the dynamic H-1 NMR spectroscopy shows that the exchange of TI+ between the two crown sides of the complexed ligand proceeds through an intramolecular tunneling. An Arrhenius convex curve was observed for intramolecular exchange. This phenomenon is explained in terms of two conformer state formations differentiated by hydrogen bond association.

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