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Org Biomol Chem ; 2(11): 1582-6, 2004 Jun 07.
Article in English | MEDLINE | ID: mdl-15162208

ABSTRACT

Two-armed neutral anion receptors (4,5), were prepared and examined for their anion-binding ability using UV-vis, fluorescence and 1H NMR spectra in DMSO. The results of non-linear curve fitting indicate that 4 or 5 form 1 : 1 stoichiometric complexes with dicarboxylate anions by multiple hydrogen bonding interactions and the sensitivity for recognition of dicarboxylate depends on the chain length of these dicarboxylate anions. Receptors 4 and 5 have no binding ability with acetate, dihydrogen phosphate and the halogen (Cl-, Br-, I-) anions. This demonstrates that receptors 4 or 5 could be used as chemical sensors for some special dicarboxylate anions.


Subject(s)
Amides/chemistry , Calixarenes , Carboxylic Acids/chemistry , Phenols/chemistry , Thiourea/chemistry , Amides/metabolism , Anions/chemistry , Anions/metabolism , Carboxylic Acids/metabolism , Molecular Structure , Phenols/metabolism , Thiourea/metabolism
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