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Facile formation of the ditelluride [(TePiPr2NiPr2PTe-)2], which exists as a centrosymmetric dimer (see picture: Te green, P purple, N blue, C gray) with a weak TeTe bond, embodies a new feature of the chemistry of dichalcogenoimidodiphosphinate ligands. The monotelluride HPiPr2NiPr2PTe analogue is obtained as the PH tautomer.
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Chivers et al. (2005) studied this question.
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