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

Atsushi Ikeda, Seiji Shinkai

Research output: Contribution to journal › Article

60 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 languageEnglish
Pages (from-to)7385-7388
Number of pages4
JournalTetrahedron Letters
Volume33
Issue number48
DOIs
Publication statusPublished - Nov 24 1992

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Complexation
Cations
Metals
Oxygen
Benzene
Cones

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Unusually high ionophoricity of 1,3-alternate-calix[4]arenes : π-Donor participation in the complexation of cations? / Ikeda, Atsushi; Shinkai, Seiji.

In: Tetrahedron Letters, Vol. 33, No. 48, 24.11.1992, p. 7385-7388.

Research output: Contribution to journal › Article

Ikeda, A & Shinkai, S 1992, 'Unusually high ionophoricity of 1,3-alternate-calix[4]arenes: π-Donor participation in the complexation of cations?', Tetrahedron Letters, vol. 33, no. 48, pp. 7385-7388. https://doi.org/10.1016/S0040-4039(00)60194-6
Ikeda A, Shinkai S. Unusually high ionophoricity of 1,3-alternate-calix[4]arenes: π-Donor participation in the complexation of cations? Tetrahedron Letters. 1992 Nov 24;33(48):7385-7388. https://doi.org/10.1016/S0040-4039(00)60194-6
Ikeda, Atsushi ; Shinkai, Seiji. / Unusually high ionophoricity of 1,3-alternate-calix[4]arenes : π-Donor participation in the complexation of cations?. In: Tetrahedron Letters. 1992 ; Vol. 33, No. 48. pp. 7385-7388.
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