The synthetic route to the η2-hydrazine–samarium complex 1 parallels protonations which were postulated for the N2 fixation in biological systems. Thus 1 was formed by a double H +-transfer onto the bridging (N2H2)2− ligand of the dinuclear complex 2. The hydrazine ligand is bound firmly to the Sm center and cannot be removed by either vacuum or recrystallization in potentially coordinating solvents.
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Evans et al. (1992) studied this question.
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