Sensing anionic species in competitive aqueous media is a well-recognised challenge to long-term applications across a multitude of fields. Herein, we report a comprehensive investigation of the electrochemical
anion sensing performance of novel
halogen bonding (XB) and hydrogen bonding (HB) bis-
ferrocene-(iodo)
triazole receptors in
solution and at self-assembled monolayers (
SAMs), in a range of increasingly competitive aqueous organic
solvent media (
ACN/H2 O). In
solution, the XB sensor notably outperforms the HB sensor, with substantial
anion recognition induced cathodic voltammetric responses of the
ferrocene/
ferrocenium redox couple persisting even in highly competitive aqueous
solvent media of 20 % water content. The response to halides, in particular, shows a markedly lower sensitivity to increasing water content associated with a unique halide selectivity at unprecedented levels of
solvent polarity. The HB sensor, in contrast, generally displayed a preference towards oxoanions. A significant surface-enhancement effect was observed for both XB/HB receptive films in all
solvent systems, whereby the HB sensor generally displayed larger responses towards oxoanions than its
halogen bonding analogue.