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Published on: May 26, 2019
Formation of heterobimetallic zirconium/cobalt diimido complexes via a four-electron transformation
Bing Wu1, Raúl Hernández Sánchez, Mark W Bezpalko
1Department of Chemistry, Brandeis University , 415 South Street, MS 015, Waltham, Massachusetts 02454, United States.
Abstract:
The reactivity of the reduced heterobimetallic complex Zr((i)PrNP(i)Pr2)3CoN2 (1) toward aryl azides was examined, revealing a four-electron redox transformation to afford unusual heterobimetallic zirconium/cobalt diimido complexes. In the case of p-tolyl azide, the diamagnetic C3-symmetric bis(terminal imido) complex 3 is formed, but mesityl azide instead leads to asymmetric complex 4 featuring a bridging imido fragment.
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