(C) 2001 Elsevier Science B.V. All rights reserved.The main focus of this r
eview is the self-assembly in aqueous solutions of bowl-shaped sodium p-sul
fonatocalix[4,5]arenes with main group, transition metal and lanthanoid spe
cies, and with various organic molecules as additional supramolecular build
ing components, for example 18-crown-6, and other macrocycles, pyridine N-o
xide, amino-acids, and more. The versatility of building up new materials b
ased on these components is demonstrated by the formation of a diverse rang
e of complex inclusion structures assembled through pi -stacking, hydrogen
bonding and coordination interactions. There are up-down arrangements of ca
lix[4]arenes in hydrophobic -hydrophobic bi-layer structures with the posit
ively charged species and included molecules between the layers. A variant
of this is prevalent in structures incorporating 18-crown-6 which, in essen
ce, are built up of globular superanions or ionic capsules, for example {Na
+ subset of (18-crown-6)(H2O)(n)} subset of {(p-sulfonatocalix[4]arene(4=))
(2)}(7 -), n = 0 or 2. These can crystallize, often selectively, polynuclea
r hydrolytic M(III) cations [M-2(OH)(2)(H2O)(8)](4+), [M-3(OH)(4)(H2O)(10)]
(5+), [M4OH)(6)(H2O)(12)](6+), M = Cr or Rh, or [Al13O4(OH)(24)(H2O)(12)](7
+), depending on the pH and other synthetic parameters. Lanthanide(III) ion
s form a range of complexes at specific pH in the presence of the calixaren
e and crown ether, including complexes containing the capsule [{18-crown-6}
subset of {M(H2O)(7)(3+))(1.33)(p-sulfonatocalix[4]arene(4-))}(2)], for th
e smaller lanthanides, or the Ferris-wheel type structure [{La3+ subset of
(18-crown-6)(OH2)(3)} boolean AND {(p-sulfonatocalix[4]arene(4=) + 2H(+))}]
(+), for the larger lanthanide. In the presence of pyridine N-oxide, at pH
4 where the calixarenes take on 5 - charge, an up-up arrangement of sulfona
ted calixarenes results, either assembled in icosahedral spheres, or infini
te chiral, helical nano-tubes.