z-logo
Premium
Syntheses, Structures, and Anion‐Binding Properties of Two Novel Calix[2]benzo[4]pyrroles
Author(s) -
Cafeo Grazia,
Kohnke Franz H.,
White Andrew J. P.,
Garozzo Domenico,
Messina Angela
Publication year - 2007
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200600452
Subject(s) - pyrrole , counterion , chemistry , benzene , phenylene , acetone , ion , fluoride , medicinal chemistry , polymer chemistry , organic chemistry , inorganic chemistry , polymer
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 n Bu 4 N + counterion) were also determined.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom