Polyaza metacyclophanes as ditopic anion receptors

Ilioudis, C.A.; Steed, J.W.

Abstract

Five macrocyclic polyaza metacyclophanes L-1 - L-5 prepared by dipode coupling of the tosylated precursors have been studied. The basicity of the ligands has been measured potentiometrically and their ability to complex halides and perchlorate has been studied in the solid state by X-ray crystallography. The results reveal that the ligands generally act as ditopic halide receptors with even the largest, L5, being too small to envelop the anion. The ligand's basicity behaviour parallels that observed for related para-analogues. Despite the ready crystallisation o fluoride, HF2-, chloride, bromide, iodide and triiodide salts in the solid state, there appears to be little afinity for halides in aqueous solution in the pH range accessible via potentiometry. The results do give a detailed insight into the role of the aryl ring in restricting the conformational. exibility of the ligands and, hence, the ability to chelate perching anions.

Citation

Ilioudis, C., & Steed, J. (2005). Polyaza metacyclophanes as ditopic anion receptors. Organic and Biomolecular Chemistry, 3(16), 2935-2945

• Journal Article Type: Article
• Publication Date: 2005
• Journal: Organic and Biomolecular Chemistry
• Print ISSN: 1477-0520
• Electronic ISSN: 1477-0539
• Publisher: Royal Society of Chemistry
• Peer Reviewed: Peer Reviewed
• Volume: 3
• Issue: 16
• Pages: 2935-2945
• Public URL: https://durham-repository.worktribe.com/output/1602026