TY - JOUR
T1 - Synthesis, Structure and Alkali Metal Ion Binding Properties of a Podand Polyether Derived from Calix[4]arene, 5,11,17,23-tetra-tert-butyl-25,27-di(phenylmethoxy)-26,28-di(2'-methoxyethoxy)-calix[4]arene
AU - Abidi, R.
AU - Harrowfield, J.M.
AU - Skelton, Brian
AU - White, Allan
AU - Asfari, Z.
AU - Vicens, J.
PY - 1997
Y1 - 1997
N2 - The ligand 5,11,17,23-tetra-t-butyl-25,27-di(phenylmethoxy)-26,28-di(2-methoxyethoxy)calix[4]arene, designed as an analogue of some calixcrown species in order to evaluate possible origins of their selectivity in alkali metal ion binding, has been synthesised and structurally characterised by X-ray crystallography. The crystals are monoclinic, P2(1)/n, a = 15.940(6), b = 19.388(5), c = 20.020(5) Angstrom, beta = 109.10(2) deg., Z = 4, conventional R on \F\ being 0.073 for 3454 independent, 'observed' (I > 3 sigma(I)) reflections. H-1-NMR studies in 1:1 CD3CN/CDCl3 solvent have shown that the ligand exerts a strong preference for the lighter alkali metal ions (Li+ and Na+) contrary to the binding behaviour of known calixcrowns. This may reflect interactions restricted to the lower rim donor atoms without concomitant interaction with the calixarene pi-electrons, perhaps because the latter interactions are substituted by those with the benzyl group pi-electrons.
AB - The ligand 5,11,17,23-tetra-t-butyl-25,27-di(phenylmethoxy)-26,28-di(2-methoxyethoxy)calix[4]arene, designed as an analogue of some calixcrown species in order to evaluate possible origins of their selectivity in alkali metal ion binding, has been synthesised and structurally characterised by X-ray crystallography. The crystals are monoclinic, P2(1)/n, a = 15.940(6), b = 19.388(5), c = 20.020(5) Angstrom, beta = 109.10(2) deg., Z = 4, conventional R on \F\ being 0.073 for 3454 independent, 'observed' (I > 3 sigma(I)) reflections. H-1-NMR studies in 1:1 CD3CN/CDCl3 solvent have shown that the ligand exerts a strong preference for the lighter alkali metal ions (Li+ and Na+) contrary to the binding behaviour of known calixcrowns. This may reflect interactions restricted to the lower rim donor atoms without concomitant interaction with the calixarene pi-electrons, perhaps because the latter interactions are substituted by those with the benzyl group pi-electrons.
U2 - 10.1023/A:1007981710765
DO - 10.1023/A:1007981710765
M3 - Article
VL - 27
SP - 291
EP - 302
JO - Journal of Inclusion Phenomena and Molecular Recognition in Chemistry
JF - Journal of Inclusion Phenomena and Molecular Recognition in Chemistry
ER -