Reactions of each Cp2Zr(Me)Cl and Cp2ZrCl2 with PhC=CCH2MgBr afford the eta
(3)-propargyl/allenyl complexes Cp2Zr(Me)(eta(3)-CH2CCPh) (I) and Cp2Zr(CH2
CCPh)(2) (2), respectively. Both products were characterized by a combinati
on of EI mass spectrometry and H-1- and C-13-NMR spectroscopy, and the stru
cture of 1 was elucidated by a single-crystal X-ray analysis. Molecules of
1 contain an unsymmetrically ligated eta(3)-propargyl/allenyl group C(1)H2C
(2)C(3)Ph with Zr-C(1)=2.658(4), Zr-C(2) = 2.438(3) and Zr-C(3) = 2.361(3)
Angstrom. Within the CH2CCPh ligand, C(1)-C(2) = 1.344(5), C(2)-C(3) = 1.25
9(4) Angstrom and C(1)-C(2)-C(3)= 155.3(3)degrees. The latter set of data i
ndicates that a sigma, pi-allenyl resonance structure makes a relatively la
rge contribution to the bonding description in 1 compared to a sigma, pi-pr
opargyl resonance structure. The fragment ZrC(10)C(I)C(2)C(3) (C(10)= C of
Me) is contained essentially in the mirror plane that reflects the two Cp r
ings. Complex 1 shows no fluxional behavior in its H-1-NMR spectra over the
temperature range 303-223 K. In contrast, 2 is fluxional, and its dynamic
behavior persists on cooling even to 180 K. The H-1-NMR spectra suggest tha
t a rapid exchange of the modes of bonding of eta(3)-propargyl/allenyl and
eta(1)-propargyl ligands may occur, with a probable participation of anothe
r Zr-C3H2Ph bonding mode, possibly eta(1)-allenyl. (C) 2000 Elsevier Scienc
e S.A. All rights reserved.