“…The selectivity of these ligands toward caesium is so high that they are better Cs + sensors than any other functionalized calix (Pérez-Jiménez et al, 1998). Molecular Dynamics calculations as well as X-ray crystallographic data suggest that, provided no steric hindrance is introduced in the polyether bridge(s), hydrophobic interactions exist between the extracted alkali cations and the π electrons of the aryl rings, hence favouring the binding of the less hydrated caesium cation as compared to harder alkali cations, such as sodium (Wipff and Lauterbach, 1995, Lauterbach and Wipff, 1996, Thuery et al, 1996, Lamare et al, 1997, 1998, Jankowski et al, 2003. As expected, although unusual in metallic complexation, the symmetrical arrangement of calix[4]arenes-biscrown-6 with two complexing cavities, is well adapted to the formation of both 1 : 1 (ligand : metal) and 1 : 2 complexes, as indicated by NMR, electro-spray ionization mass spectrometry (ESI-MS), and X-ray crystallographic studies (Arnaud-Neu et al, 1996, Allain et al, 2000.…”