Unusually high ionophoricity of 1,3-alternate-calix[4]arenes: π-Donor participation in the complexation of cations?

Atsushi Ikeda; Seiji Shinkai

doi:10.1016/S0040-4039(00)60194-6

Unusually high ionophoricity of 1,3-alternate-calix[4]arenes: π-Donor participation in the complexation of cations?

Atsushi Ikeda, Seiji Shinkai

Institute for Advanced Study

Research output: Contribution to journal › Article › peer-review

61 Citations (Scopus)

Abstract

It was found that 1,3-alternate-calix[4]arenes having cavities composed of two oxygens and two benzene rings show the metal affinity much higher than cone-calix[4]arenes having a cavity composed of four oxygens. The unexpected finding is most likely rationalized in terms of the "π-donor participation" in the metal complexation.

Original language	English
Pages (from-to)	7385-7388
Number of pages	4
Journal	Tetrahedron Letters
Volume	33
Issue number	48
DOIs	https://doi.org/10.1016/S0040-4039(00)60194-6
Publication status	Published - Nov 24 1992

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)60194-6

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AB - It was found that 1,3-alternate-calix[4]arenes having cavities composed of two oxygens and two benzene rings show the metal affinity much higher than cone-calix[4]arenes having a cavity composed of four oxygens. The unexpected finding is most likely rationalized in terms of the "π-donor participation" in the metal complexation.

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Unusually high ionophoricity of 1,3-alternate-calix[4]arenes: π-Donor participation in the complexation of cations?

Abstract

All Science Journal Classification (ASJC) codes

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