Two new titanium complexes of the general type Ti(η5:η1‐C5H4SiMe2NCH2CH2X)Cl2 (X = NMe2 OMe), containing a tridentate ligand, were prepared by reaction of Ti(η5‐C5H4SiMe2Cl)Cl3 with the lithium amide Li(NHCH2CH2X) (X = NMe2, OMe). The 1HNMR chemical shifts for the protons of the ethylene link were found to vary considerably as a function of the temperature, indicating the presence of an equilibrium between the tri‐ and bidentate bonding mode of the ligand. A single‐crystal X‐ray structural analysis of Ti(η5:η1C5H4SiMe2NCH2CH2OMe)Cl2 revealed that the methoxy function is not intramolecularly coordinated in the solid state.
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Okuda et al. (1996) studied this question.
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