Keywords
diphenylmethanides
oxidative coupling
rare-earth metals
structure
synthesis
Abstract
The outcome of salt metathesis reactions between the equimolar amounts of LnCl3 and dimeric potassium diphenylmethanide {[2,2′-(4-MeC6H3NMe2)2CH]K(THF)}2 depends on the rare-earth metal ion. In the case of ScIII and YIII, the reactions afford chlorido-bis(diphenylmethanido) complexes {[2,2′-(4-MeC6H3NMe2)2CH]2LnIII(μ-Cl)}2, in which the diphenylmethanido ligands perform bidentate κ2-CN coordination according to the X-ray data. For YbIII and SmIII, these reactions result in the spontaneous reduction of LnIII to LnII and the formation of known bis(diphenylmethanido) complexes [2,2′-(4-MeC6H3NMe2)2CH]2LnII and the product of oxidative coupling of diphenylmethanido anions.
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