Abstract

The synthesis of acyclic and macrocyclic transition metal dithiocarbamate complexes containing positively charged imidazolium moieties is reported. The assemblies have been characterised by a range of spectroscopic techniques and the ability of these compounds to bind various anions was also examined. UV–Vis spectroscopic binding studies revealed H 2 P O 4 - is complexed selectively in preference to F − and Cl − for the acyclic transition metal dithiocarbamate complexes containing the N-methylimidazolium moiety. Cyclic voltammetric studies demonstrated that the copper(II) dithiocarbamate imidazolium systems can electrochemically sense the binding of Cl − and H 2 P O 4 - .

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