Protonation and Deprotonation of TpOs(NHPh)Cl2:  An Unusually Inert Amido Ligand

• Published in: Inorganic chemistry 2001-04, Vol.40 (8), p.1888-1893
• Main Authors: Soper, Jake D, Bennett, Brian K, Lovell, Scott, Mayer, James M
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic001177x

Protonation of the Os(IV) amido complex TpOs(NHPh)Cl2 (1) to give the aniline complex [TpOs(NH2Ph)Cl2]OTf (2) requires excess triflic acid (HOTf). Complex 1 is unreactive with HCl and other moderately strong acids. Consistent with the low basicity of 1, the aniline complex 2 is extremely acidic and is deprotonated by stoichiometric addition of weak bases such as Cl- or H2O. No reaction is observed between 1 and methyl triflate (CH3OTf) at ambient temperatures. Upon heating, CH3OTf removes the chloride ligands from 1 to give CH3Cl and the amidobis(triflate) complex TpOs(NHPh)(OTf)2 (3). Attack at the amido nitrogen is not observed. Complex 1 is thus very inert to protonation and electrophilic attack at nitrogen. A deprotonated form of 1, TpOs[NPh(MgBr)]Cl2 (4), is generated on reaction of PhMgBr with TpOs(N)Cl2. Complex 4 is extremely basic and will protonate to 1 with weak acids such as CH3CN, DMSO, and acetic anhydride. Thus, 1 has a low acidity as well as a low basicity; it is both less acidic and less basic than aniline. The inertness of 1 is ascribed to partial Os−N π bonding and to the oxidizing nature of the Os(IV) center.