The crystallographically determined structural features of Na(isodiCp)(15-crown-5) and [K-cryptand(2.2.2)]+(isodiCp)- are compared to those of the corresponding Li(TMEDA) complex and the sandwich dimer involving Li+ (cocrystallized with Li(12-crown-4)2). The features of the potassium salt are distinctively different from those of its congeners. As a consequence of the encapsulation of the K+ ion by the cryptand, no interaction occurs with the isodiCp anion, which is “naked”. Notwithstanding the complete dissociation that exists, the stand-alone isodiCp anion exhibits appreciable folding about the bond that it shares with the norbornyl framework. The dihedral angle is 8.3(1)° in a downward direction away from the exo surface. This unrivaled opportunity to observe the free isodicyclopentadienide anion is shown to be in agreement with the results of HF−SCF calculations.

The diastereomeric endo and exo isomers of the title complex, [TiCl3(C10H11)], have been synthesized by electrophilic attack of TiCl4 on the exo- or endo-trimethylsilyl derivative of isodiCp (isodiCp = isodicyclopentadiene). This reaction proceeds with net inversion of configuration to give exclusively either the endo- or exo-(isodiCp)TiCl3 compound. Although the two isomers have similar unit-cell constants, they crystallize in different space groups. The endo complex, (2), is in Pbcm with a crystallographic mirror plane, while the exo complex, (4), is in Pca2(1) with pseudo-mirror symmetry. Both molecules display a distorted tetrahedral geometry about the Ti atom. Each Ti atom is bonded in a eta(5) manner to the Cp ring of the isodiCp ligand, with Ti--ring centroid distances of 2.031 (2) and 2.013 (2) A for (2) and (4), respectively. A slight bending of the isodiCp ligand about the bond shared by the Cp ring and the norbornane fragment is observed in both structures. The determination of the absolute structure of (4) defines the directionality of the packing along the polar c axis.

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The mu-oxo dimer mu-oxo-bis[dichloro[(1,2,3,3a,7a-eta)- 4,5,6,7-tetrahydro-4,7-methano-1H-indenyl]titanium], [Ti2Cl4(mu-O)(C10H11)2], and the mu-oxo cyclic tetramer, cyclo-tetra-mu-oxo-tetrakis[chloro[(1,2,3,3a,7a-eta)-4,5,6,7-tetrahydro- 4,7-methano-1H-indenyl]titanium], [Ti4Cl4(mu-O)4(C10H11)4], have been synthesized by electrophilic attack of TiCl4 on the exo-trimethylsilyl derivative of isodiCp (isodiCp is the isodicyclopentadienide anion or 4,5,6,7-tetrahydro-4,7-methano-1H-indene) in the presence of trace amounts of moisture. Both structures are endo isomers, with each Ti atom bonded in a eta 5 manner to the Cp ring of the isodiCp ligand. Both display a slight bending of the isodiCp group about the bond common to the Cp ring and the norbornane fragment, such that the norbornane group is displaced in the direction away from the Ti atom. The dihedral angles which describe this bending are 9.0 (3) and 10.2 (3) degrees for the dimer, and 9.2 (2) degrees for the tetramer. The dimer contains a bent Ti-O-Ti angle of 159.5 (2) degrees. The tetramer forms tetragonal crystals, which are twinned by merohedry on the (110) plane. The tetramer molecule contains a crystallographic 4 axis, with the Ti atoms linked by the O atoms in a mu-oxo manner to form an eight-membered ring.

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