Abstract
A simple, readily-prepared precipitant (1.Cl2) precipitates oxalate or terephthalate from water with very high efficacy, removing these anions at sub-millimolar concentrations using only one equivalent of precipitant. A simple aqueous base/acid cycle can be used to regenerate 1.Cl2 after use. The resulting precipitates, 1.oxalate and 1.terephthalate, are anhydrous and closely-packed, with each anion receiving eight charge-assisted hydrogen bonds from amidinium N–H donors. Precipitation of oxalate and terephthalate occurs at much lower concentrations than other dicarboxylates, and direct competition experiments with the biologically/environmentally relevant divalent anions CO32–, HPO42– and SO42– reveal very high selectivity for oxalate or terephthalate over these competitors.
Supplementary materials
Title
Supporting Information
Description
Details of synthesis and characterisation, precipitation experiments, solubility measurements, precipitant regeneration, anion chromatography and X-ray crystallography.
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