Iron complexation by biomass model compounds†

Abstract

Iron chelating agents have important roles to play, both in human physiology and in the environment. In the latter case, persistence in the environment has given cause for concern in the case of synthetic iron chelating agents such as ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA), which do not readily biodegrade. Due to their long lifespan in the environment synthetic iron chelators can also participate in mobilization reactions, particularly with radionuclides such as ⁶⁰Co. There is an eminent need to explore alternative iron chelating compounds, preferably, renewable in origin, to overcome the drawbacks of synthetic compounds, making plant biomass a potential source of iron chelating agents. Twelve biomass model compounds, representative of the biomass constituents, cellulose, hemicellulose, lignin and extractives (tannins), were tested for their iron complexation ability by measurement of the binding strengths with Fe(II) and Fe(III) in dimethylsulfoxide (DMSO), to ensure solubility, using spectrophotometric titration. The flavonols, kaempferol, quercetin and myricetin displayed the strongest binding affinity to Fe(II) and Fe(III) along with the greatest positive cooperativity as determined by the calculation of Hill coefficients. The lignin-representative compound, p-coumaric acid, showed the highest binding affinity to Fe(II) only. Carbohydrate model compounds did not show any evidence of binding to iron, despite some contrary evidence in literature about their ability to do so. This study points to the potential role that the flavonols class of compounds, and therefore by extension, plant tissues that are rich in extractives, may play in the exploration of biomass-derived iron chelants.