“…These metals were selected because they should proceed spontaneously in both aqueous and DES systems from their redox potentials. Additionally, the Cu(II) and Fe(III) species present in these chloride‐based DESs and brines are already well‐characterised via spectroscopy
[3,13,20,39–40] . In both cases, each molar equivalent of oxidising agent will remove one electron from the target metal, so for a general process, x moles of Cu II or Fe III will be required per oxidation state number of the oxidised form of the target metal:
…”