4.6 Article

Syntheses, structures, and anion-binding properties of two novel calix[2]benzo[4]pyrroles

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 13, Issue 2, Pages 649-656

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200600452

Keywords

anions; calixpyrroles; host-guest systems; macrocycles; structure elucidation

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Calix[2]benzo[4]pyrrole m-6 and p-6, each containing two dipyrromethane moieties and two m-phenylene or p-phenylene units, respectively, were readily synthesised from pyrrole, 1,3- and 1,4-bis(1,1'-dimethylhydroxymethyl)benzene, (m-4 and p-4, respectively) and acetone. Macrocycles m-6 and p-6 were tested as receptors for a selection of anions, such as acetate, dihydrogenphosphate and fluoride. The X-ray structures of m-6 and p-6 and those of the complexes m-6(.)F(-), m-6(.)Cl(-) and m-6(.)CH(3)COO(-) (with an nBu(4)N(+) counterion) were also determined.

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