Abstract
The proton coupled electron transfer reactivity of an octahedral Ta(V) aniline complex ligated by an acridane-derived redox active NNN pincer ligand is reported. Reversible association of aniline to a Ta(V) dichloride leads to significant coordination induced bond weakening of aniline’s N–H bonds allowing for two-fold hydrogen atom abstraction yielding a terminal imido complex accompanied by two-electron oxidation of the NNN pincer ligand under retention of the metal oxidation state. The bond dissociation free energies of the amine and a transient radical amido complex are estimated via stoichiometric reactions with hydrogen atom abstractor and donor reagents complemented by DFT calculations.
Supplementary materials
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Supporting Information
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Synthetic, crystallographic, spectroscopic and computational details
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Checkcif
Description
Checkcif files of all XRD structures
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.cif files of 3
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crystallographic file of compounds 3
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.cif file of 4
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crystallographic file of compounds 4
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.xyz files of all computed structures
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Coordinates of all computed structures
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