Abstract

Synthetic and structural studies have been performed for two imido complexes of titanium(IV). The reaction between [{Ti(NBut)Cl2(NH2But)2}3] and 6 equivalents of Me3SiN3 at room temperature in the presence of pyridine resulted in the substitution of only one chloride per titanium atom and formation of the dimeric complex [{Ti(NBut)Cl(N3)(py)2}2] (py = pyridine). An alternative approach to such complexes, which involved the reaction between [Ti(NMe2)2(N3)2(py)2] and 1 equivalent of CyNH2 at room temperature, resulted in the dimeric bis(azide) complex [{Ti(NCy)(N3)2(py)2}2] (Cy = cyclohexyl). The two new complexes have been characterised by X-ray crystallography; the solid state of each comprises dimeric units in which the two titanium atoms are bridged by a pair of azide ligands. A gas-phase pyrolysis study has been conducted on [Ti(NMe2)2(N3)2(py)2] and preliminary CVD experiments on the two new complexes revealed that they are not effective titanium nitride precursors.

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