Stevens, James Rawiri2012-04-042012-04-042011http://hdl.handle.net/10179/3192The investigation into neutral aryl-linked oxime dicopper helicates encapsulating a number of anions was carried out. Two dicopper aryl-linked salicyloxime derived complexes were synthesized and studied which contained either p-xylylic (1) or m-xylylic (2) incorporated spacer groups. UV-visible spectroscopy was used to determine the binding stability constants of the anion complexes. Complex binding, encapsulation of anions and the conformational flexibility of 1 and 2 was supported and ascertained by the crystal structural data obtained. Receptor 1 expressed an exceptional binding strength for sulfate in THF where a log K value of 5.5 ± 0.3 was acquired. Receptor 2 could form both helical and non-helical structures. This was able to bind bromide selectively in a 2:1 stoichiometry of anion:receptor with a log K2 value of 9.2 ± 0.1 and showed an unexpectedly high association constant for the perchlorate anion in a 1:1 stoichiometry with a log K value of 4.6 ± 0.2 (presumably in a helical structure).enThe AuthorAnionsSupramolecular chemistryThesisQ112887973https://www.wikidata.org/wiki/Q112887973