A. Alvanipour et al., SOME CROWN-ETHER CHEMISTRY OF TI, ZR AND HF DERIVED FROM LIQUID CLATHRATE MEDIA, Journal of the Chemical Society. Dalton transactions, (7), 1998, pp. 1223-1228
The reaction of [Ti(eta-C5H5)(2)Cl-2] with HCl(g) in the presence of 1
8-crown-6 formed the oxonium ion-containing complex [H3O+. 18-crown-6]
[TiCl5(H2O)(-)] 1. Its crystal structure shows the oxonium ion resides
within the crown ether and has a pyramidal structure. Treatment of [T
i(eta-C5H5)Cl-3] with AlMe3 in the presence of 18-crown-6 resulted in
the formation of the titanium(III) complex [Ti(eta-C5H5)Cl+. 18-crown-
6][AlCl2Me2] 2. The structure of 2 reveals a cation with a five-co-ord
inate Ti where the centroid of the C5H5 ring occupies the apex of a sq
uare pyramid. The crown ether 18-crown-6 underwent C-O bond scission b
y treatment with ZrCl4 in the presence of thf (tetrahydrofuran) to for
m the ring-opened zirconium(IV) co-ordination complex [ZrCl2 .(OCH2CH2
)(5)OCH2-CH2Cl+][ZrCl5(thf)(-)] 3. The structure of 3 shows the format
ion of a zirconium alkoxide species formed by the ring-opening reactio
n. The seven-co-ordinate zirconium center has pentagonal-bipyramidal g
eometry with two chloride atoms in the axial positions. In an analogou
s reaction, but in the presence of NaCl, HfCl4 formed the ionic comple
x [Na+. 18-crown-6][HfCl5(thf)(-)] 4, which has a structure similar to
that of 1.