Issue 3, 1998

Synthesis and lithium ion selectivity of 14-crown-4 derivatives having bulky subunits: cis and trans isomers of 2-phenylcyclohexano-14-crown-4, 2,3-diphenylcyclohexano-14-crown-4 and 2,3-di-(1-adamantyl)-14-crown-4

Abstract

cis- and trans-2-Phenylcyclohexano-14-crown-4, cis- and trans-2,3-diphenylcyclohexano-14-crown-4, and cis- and trans-2,3-di-(1-adamantyl)-14-crown-4 have been prepared and their ion selectivities toward alkali metal cations examined by means of the extraction of alkali metal picrates, the measurement of stability constants of the complexes with lithium or sodium perchlorate, and the electrode response potential measurement for the ion-sensitive membranes. The remarkable dependence of the complexation ability to Li+ on the cis/trans stereochemistry of the ionophores is discussed on the basis of their geometries estimated by molecular mechanics calculations and the structures of cis- and trans-diphenylcyclohexano derivatives determined by X-ray structure analyses. In order to assist the discussion, the X-ray structure analyses of the lithium picrate complex of decalino-14-crown-4 and the 2∶1 ‘sandwich-type’ complex of benzo-14-crown-4 with sodium perchlorate have also been undertaken.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 485-494

Synthesis and lithium ion selectivity of 14-crown-4 derivatives having bulky subunits: cis and trans isomers of 2-phenylcyclohexano-14-crown-4, 2,3-diphenylcyclohexano-14-crown-4 and 2,3-di-(1-adamantyl)-14-crown-4

Y. Tobe, Y. Tsuchiya, H. Iketani, K. Naemura, K. Kobiro, M. Kaji, S. Tsuzuki and K. Suzuki, J. Chem. Soc., Perkin Trans. 1, 1998, 485 DOI: 10.1039/A706606F

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