Synthesis and 1H NMR studies of vinyl-substituted calix[4]arene derivatives

Enhanced cation-π interactions with extended calix[4]arene π-systems

Pavel Lhotak, Ryoji Nakamura, Seiji Shinkai

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A new class of calix[4]arene derivatives bearing vinyl groups on the upper rim has been synthesized using the condensation of starting 5,17-diformyl-2526,27,28-tetrapropoxycalix[4]arene with malonic acid in the presence of piperidine as a catalyst. The corresponding vinyl substituted derivative can be isolated directly in 40% yield and serves as a starting point for the preparation of calix[4]arene derivatives fixed either in the cone or 1,3-alternate conformations. The complexation ability of such compounds towards Ag+ cation has been studied with the help of 1H NMR spectroscopy and MS spectroscopy. It was shown that the presence of the double bonds at upper rim can enhance binding constants as compared with unsubstituted derivatives due to their additional cation-π interactions. The significance of the double bonds for quaternary pyridinium salts has been also demonstrated by the enhanced binding ability.

Original languageEnglish
Pages (from-to)333-344
Number of pages12
JournalSupramolecular Chemistry
Volume8
Issue number4
DOIs
Publication statusPublished - Jan 1 1997

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Cations
Nuclear magnetic resonance
Derivatives
Bearings (structural)
Complexation
Nuclear magnetic resonance spectroscopy
Conformations
Cones
Condensation
Salts
Spectroscopy
Catalysts
calix(4)arene

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Synthesis and 1H NMR studies of vinyl-substituted calix[4]arene derivatives : Enhanced cation-π interactions with extended calix[4]arene π-systems. / Lhotak, Pavel; Nakamura, Ryoji; Shinkai, Seiji.

In: Supramolecular Chemistry, Vol. 8, No. 4, 01.01.1997, p. 333-344.

Research output: Contribution to journalArticle

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