Incorporation of [CpRh] and [CpIr] Species into Heterobimetallic Complexes via Protonolysis Reactivity and Dioximato Chelation

• Published in: Inorganic chemistry Vol. 60; no. 18; pp. 14047 - 14059
• Main Authors: Kumar, Amit, Comadoll, Chelsea G, King, Daniel S, Oliver, Allen G, Day, Victor W, Blakemore, James D
• Format: Journal Article
• Language: English
• Published: American Chemical Society 20-09-2021
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.1c01362

The synthesis of multimetallic compounds can enable the placement of two or more metals in close proximity, but efforts in this area are often hindered by reagent incompatibilities and a lack of selectivity. Here, we show that organometallic half-sandwich [Cp*M] (M = Rh, Ir) fragments (where Cp* is η5-pentamethylcyclopentadienyl) can be cleanly installed into metallomacrocyclic structures based on the workhorse diimine–monooxime–monooximato ligand system. Six new heterobimetallic compounds have been prepared to explore this synthetic chemistry, which relies on in situ protonolysis reactivity with precursor Ni­(II) or Co­(III) monometallic complexes in the presence of suitable [Cp*M] species. Solid-state X-ray diffraction studies confirm installation of the [Cp*M] fragments into the metallomacrocycles via effective chelation of the Rh­(III) and Ir­(III) centers by the nascent dioximato site. Contrasting with square-planar Ni­(II) centers, the Co­(III) centers prefer octahedral geometry in the heterobimetallic compounds, promoting bridging ligation of acetate across the two metals. Spectroscopic and electrochemical studies reveal subtle influences of the metals on each other’s properties, consistent with the moderate M′···M distances of ca. 3.6–3.7 Å in the modular compounds. Taken together, our results show that heterobimetallic complexes can be assembled with organometallic [Cp*M] fragments on the diimine–dioximato platform.