Solvent effect on neutral chiral supramolecular assemblies and their distinct receptor behaviour towards anions†
Abstract
We describe the distinct receptor behaviour of a neutral chiral Cu(II) complex in dimethylsulfoxide or methanol towards anions, such as F−, Cl−, Br−, I− or OAc−, where F− and OAc− show the most colorimetric change, through various spectroscopic techniques. Further insights into this at the molecular level come from the single crystal X-ray structures of both dimethylsulfoxide and methanol solvates which show a solvent effect on their supramolecular network formation. Both chromogenic and fluorogenic sensing of the anions indicate a 2 : 1 receptor–anion formation via anion–π as well as hydrogen bonding interactions.