Abstract
Data on the electrical, optical, magnetic, and structural properties of Ti2 O3 are reviewed; the differences between the transition encountered in Ti2 O3 and V2 O3 are particularly stressed. Perusal of the available experimental and theoretical work leads to the conclusion that the transition in Ti3 O3 can be explained without invoking antiferromagnetic ordering. This is of particular relevance in light of recent experimental work which casts serious doubt on the commonly accepted hypothesis that Ti2 O3 is antiferromagnetic. An alternative interpretation of the transition is offered, according to which a gradual change in the position and width of two close-lying bands results in a change of Ti2 O3 from a narrow-gap semiconductor to a semimetal. It is pointed out that a simple theory based on this model is in essential accord with the available experimental data, and that it satisfies the requirements imposed by crystal symmetry.

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