Titlebook: Calixarenes: A Versatile Class of Macrocyclic Compounds; J. Vicens,V. Böhmer Book 1991 Kluwer Academic Publishers 1991 Claisen rearrangeme

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S. Walitza,J. Seifert,A. Warnke,M. Gerlachetic acid, these small spherical cations were thought to be incapable of complex formation with any known ligand. Consequently, they were frequently used in large excess as the supporting electrolyte in studies of cation complexation in solution. The coordination chemistry of the alkali cations blos

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J. Seifert,Ch. Schubert,M. Gerlachst—guest chemistry related to calixarenes have been very limited [1–3]. In fact, Gutsche stated in his 1985 review article that there are no published data in support of solution complexes of calixarenes [2]. This is in sharp contrast to cyclodextrins which can form a variety of host—guest-type solu

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https://doi.org/10.1007/978-3-7091-3791-8 the ‘lower rim’, Y, of the calixarene, ., can lead to water-soluble species. These substances are of particular importance with regard to cation complexation [2]. The focus of this chapter is on ‘upper rim’-substituted derivatives of calix[4]arenes.

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R. Taurines,C. Wewetzer,A. Warnke,M. Gerlachs ranging from simple qualitative testing for cations [4] to major aspects of biological [5] and industrial [6] chemistry. While most early studies concerned the chemistry of aryloxide ligands and this continues to be a focus [7–10], the prominence of aryl ether units in macrocyclic systems such as

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Water Soluble Calixarene Salts. A Class of Compounds with Solid-State Structures Resembling Those of the ‘lower rim’, Y, of the calixarene, ., can lead to water-soluble species. These substances are of particular importance with regard to cation complexation [2]. The focus of this chapter is on ‘upper rim’-substituted derivatives of calix[4]arenes.

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Calixarenes: A Versatile Class of Macrocyclic Compounds978-94-009-2013-2Series ISSN 0923-6732

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0923-6732 Overview: 978-94-010-7402-5978-94-009-2013-2Series ISSN 0923-6732

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