Investigation of iron–ammine and amido complexes within a C3-symmetrical phosphinic amido tripodal ligand

• Published in: Dalton transactions : an international journal of inorganic chemistry 2021-08, Vol.50 (32), p.11197-11205
• Main Authors: Chen, Sun, Oswald, Victoria F, Hill, Ethan A, Ziller, Joseph W, Borovik, A S
• Format: Article
• Language: English
• Subjects: Ammonia; Coordination compounds; Crystallography; Donors (electronic); Ethane; Hydrogen bonds; Iron; Ligands; Toluidine
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/d1dt01032h

The primary and secondary coordination spheres can have large regulatory effects on the properties of metal complexes. To examine their influences on the properties of monomeric Fe complexes, the tripodal ligand containing phosphinic amido groups, N,N′,N′′-[nitrilotris(ethane-2,1-diyl)]tris(P,P-diphenylphosphinic amido) ([poat]3−), was used to prepare [FeII/IIIpoat]−/0 complexes. The FeII complex was four-coordinate with 4 N-atom donors comprising the primary coordination sphere. The FeIII complex was six-coordinate with two additional ligands coming from coordination of O-atom donors on two of the phosphinic amido groups in [poat]3−. In the crystalline phase, each complex was part of a cluster containing potassium ions in which K⋯O=P interactions served to connect two metal complexes. The [FeII/IIIpoat]−/0 complexes bound an NH3 molecule to form trigonal bipyramidal structures that also formed three intramolecular hydrogen bonds between the ammine ligand and the O=P units of [poat]3−. The relatively negative one-electron redox potential of −1.21 V vs. [FeIII/IICp2]+/0 is attributed to the phosphinic amido group of the [poat]3− ligand. Attempts to form the FeIII–amido complex via deprotonation were not conclusive but isolation of [FeIIIpoat(NHtol)]− using the p-toluidine anion was successful, allowing for the full characterization of this complex.