Inorganics, Vol. 14, Pages 11: Formation and Reversible Cleavage of an Unusual Trisulfide-Bridged Binuclear Pyridine Diimine Iridium Complex

Inorganics doi: 10.3390/inorganics14010011

Authors:
Max Völker
Thomas Marx
Peter Burger

Iridium pyridine diimine (PDI) complexes provide a versatile platform for highly reactive Ir–nitrido species with pronounced multiple-bond character, capable of activating H–H, C–H, Si–H, and even C–C bonds. Building on this chemistry, we extended our studies to a system with a terminal Ir–S bond, starting from our recently reported PDI–Ir–SH complex, which exhibits partial multiple-bond character. Upon addition of the 2,4,6-tri-tert-butylphenoxy radical, the corresponding phenol and a tentative Ir–S• radical intermediate are formed at ambient temperature. DFT and LNO-CCSD(T) calculations consistently reveal a low barrier for this process, with the spin density localized primarily on sulfur, accounting for subsequent S–S coupling reactions. Instead of the anticipated dimeric disulfido Ir–S2–Ir complex formed along a least-motion pathway, a trisulfido Ir–S3–Ir species was obtained, and characterized by NMR spectroscopy, X-ray crystallography and mass spectrometry. The formation mechanism of the trisulfido complex was further elucidated by DFT calculations. Remarkably, the sulfur-bridge formation is thermally reversible, regenerating the monomeric sulfanido Ir–SH complex. The origin of the hydrogen atom was investigated using H2, D2, and deuterated solvents.

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