Rkr. Jetti et al., 4-Tritylbenzoic acid. A molecular scaffold for wheel-and-axle host-guest inclusion compounds with a supramolecular axis, J CHEM S P2, 6, 2000, pp. 1223-1232
Citations number
74
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
4-Tritylbenzoic acid crystallises via the carboxy dimer supramolecular synt
hon to produce a wheel-and-axle host lattice that includes different aromat
ic solvents in its microporous framework. The clathrate structures were cha
racterised by single crystal X-ray diffraction. Solvents like xylenes, chlo
robenzene and anisole are included in a channel of cross-sectional area 42
Angstrom(2) with 2:1 host-guest stoichiometry while mesitylene occupies a c
hannel of 71 Angstrom(2) as a 1:1 clathrate. The host architecture is robus
t and yet adaptive. The carboxy dimer synthon together with the phenyl-phen
yl interactions (edge-to-face, ef and offset face-to-face, off) produce rec
urring, zigzag tapes of wheel-and-axle supermolecules. A plethora of aromat
ic ef and off motifs in the intra- and inter-tape regions modulate the cavi
ty area to accommodate solvents of different size/shape. The ability to tun
e the pore volume and still retain the target wheel-and-axle topology is a
notable feature in this family of isomorphous structures. The unsolvated ac
id adopts a different crystal packing with the triphenylmethyl groups filli
ng the voids in the structure.