Two-fold proton coupled electron transfer of a Ta(V) aniline complex mediated by a redox active NNN pincer ligand

Josh, Abbenseth, Sotirios, Pavlidis, Jasmin, Alasadi, Amanda, Opis-Basilio
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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.
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氧化还原活性 NNN 夹配体介导的 Ta(V)苯胺复合物的双质子耦合电子转移
据报道,由吖啶衍生的氧化还原活性 NNN 钳子配体连接的八面体 Ta(V)苯胺配合物具有质子耦合电子转移反应活性。苯胺与 Ta(V)二氯化物的可逆结合导致苯胺的 N-H 键在配位诱导下发生显著的键弱化,从而产生两倍氢原子抽取,生成末端亚胺络合物,同时在金属氧化态保持不变的情况下,NNN 夹配体发生双电子氧化。通过与氢原子抽取试剂和供体试剂的化学计量反应,并辅以 DFT 计算,估算出了胺和瞬时自由基亚胺络合物的键解离自由能。
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