A series of 1- and 2-substituted indenyl ligands were prepared and used in
the synthesis of [1-R-Ind](2)ZrCl2 [R = Me (2b), Et (4b), Pr-i (5b), Bu-i (
6b), SiMe3 (8b), Ph (10b), Bz (12b), 1-Naph (14b)] and [2-R-Ind](2)ZrCl2 [R
= Me (1b), Et (3b), SiMe3 (7b), Ph (9b), Bz (11b), 1-Naph (13b)] metalloce
nes. An X-ray crystallographic study of 4b and 10b showed the complexes to
be the racemic diastereomers (4b, both the R,R and S,S-enantiomers and 10b,
the S,S-enantiomer). The X-ray data together with NMR spectral data reveal
ed that the size of the substituent influenced the orientation the two inde
nyl ligands of the metallocenes. The 4b diastereomers are both found to cry
stallize with their ethyl groups syn (bis-central) with respect to each oth
er whereas the larger phenyl groups in 10b results in an anti (bis-lateral)
orientation of the indenyl ligands. (C) 2000 Elsevier Science B.V. All rig
hts reserved.