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2 Homometallic Alkoxides

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508<br />

Table 6.9 (Continued)<br />

Bond length ( ˚A) Bond angle ⊲ Ž ⊳<br />

Compound Aryloxide M–O M–O–Ar Reference<br />

[W2(di-OAr)⊲OBu t ⊳4]<br />

ethane-like, di-OAr terminally bound to each W<br />

[W(O)Cl3(Hdi-OAr)] pseudo-octahedral W with Hdi-OAr OH<br />

trans to WDO<br />

[(cyclohexanone)(thf) 2Li⊲ 2-di-<br />

OAr⊳Al(di-OAr⊳]<br />

3,3 0 -dimethyl-1,1 0 -bi-2-<br />

naphtholato<br />

3,3 0 -dimethyl-1,1 0 -bi-2naphtholato<br />

1.900 (1)<br />

1.934 (1)<br />

1.794 (5)<br />

2.262 (6)<br />

1,1 0 -bi-2-naphtholato 1.75 (1) (av.)<br />

1.96 (1)<br />

126<br />

130<br />

135<br />

(HO)<br />

xii xiii<br />

xiv<br />

119 xv<br />

i H. Sasai, T. Suzuki, N. Itoh, K. Tanaka, T. Date, K. Okamura, and M. Shibasaki, J. Am. Chem. Soc., 115, 10372 (1993).<br />

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vi T.J. Boyle, N.W. Eilerts, J.A. Heppert, and F. Takusagawa, Organometallics, 13, 2218 (1994).<br />

vii M.G. Torn, P.E. Fanwick, and I.P. Rothwell, unpublished results.<br />

viii F.R.W.P. Wild, L. Zsolnai, G. Huttner, and H.H. Brintzinger, J. Organomet. Chem., 232, 233 (1982).<br />

ix N.W. Eilerts, J.A. Heppert, M.L. Kennedy, and F. Takusagawa, Inorg. Chem., 33, 4813 (1994).<br />

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xi J.A. Heppert, S.D. Dietz, N.W. Eilerts, R.W. Henning, M.D. Morton, and F. Takusagawa, Organometallics, 12, 2565 (1993).<br />

xii J.A. Heppert, S.D. Dietz, T.J. Boyle, and F. Takusagawa, J. Am. Chem. Soc., 111, 1503 (1989).<br />

xiii S.D. Dietz, N.W. Eilerts, J.A. Heppert, and D.V. Velde, Inorg. Chem., 32, 1689 (1993).<br />

xiv M.D. Morton, J.A. Heppert, S.D. Dietz, W.H. Huang, D.A. Ellis, T.A. Grant, N.W. Eilerts, D.L. Barnes, F. Takusagawa, and D. Vander Velde, J.<br />

Am. Chem. Soc., 115, 7916 (1993).<br />

xv T. Arai, H. Sasai, K. Aoe, K. Okamura, T. Date, and M. Shibasaki, Angew. Chem. Int. Ed. Engl., 35, 104 (1996).

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