This review discusses ligands which have been shown to form stable ura
nyl complexes and to be selective for the UO22+ ion, with a view to th
e recovery of U from phosphate-containing media. The most potent urano
philes were shown to be relatively rigid macrocycles with a quasi-plan
ar arrangement of five or six ligating groups. Hence, water soluble an
d lipophilic calix[n]arenes (n = 5 or 6) have been named ''super-urano
philes'' due to their remarkable uranyl selectivity and the extremely
stable nature of their uranyl complexes.