The synthesis of a square-planar cobalt(ii) hydrido complex supported by a pyrrole-based PNP ligand has been reinvestigated and its reactivity with various small molecules examined. Preparation of the complex was accomplished by treatment of the corresponding chloride complex, [CoCl(PNP)] (PNP = anion of 2,5-bis((di-tert-butylphosphino)methyl)pyrrole), with di-iso-butylaluminum hydride (DIBAL). Reaction of [CoCl(PNP)] with other hydride sources such as NaEtBH and LiAlH resulted in mixtures of the desired Co(ii) hydride along with the reduced Co(i) species, [Co(N)(PNP)], as the primary product. The hydride complex exhibits facile migratory insertion chemistry with CO producing the corresponding Co(ii) formate complex. When the Co-H complex is reacted with nitric oxide, the first example of a cobalt nitrosyl hydride complex is produced.

Formal Cu(III) complexes bearing an oxygen-based auxiliary ligand ([CuOR] 2+ , R = H or CH 2 CF 3 ) were stabilized by modulating the donor character of supporting ligand L Y (L Y = 4-Y, N,N′-bis(2,6-diisopropylphenyl)-2,6-pyridinedicarboxamide, Y = H or OMe) and/or the basicity of the auxiliary ligand, enabling the first characterization of these typically highly reactive cores by NMR spectroscopy and X-ray crystallography. Enhanced lifetimes in solution and slowed rates of PCET with a phenol substrate were observed. NMR spectra corroborate the S = 0 ground states of the complexes, and X-ray structures reveal shortened Cu−ligand bond distances that match well with theory.

Treatment of both [CoCl(tBuPNP)] and [NiCl(tBuPNP)] (tBuPNP = anion of 2,5-bis((di-tert-butylphosphino)methyl)pyrrole) with one equivalent of benzoquinone affords the corresponding chloride complexes containing a dehydrogenated PNP ligand, tBudPNP (tBudPNP = anion of 2,5-bis((di-tert-butylphosphino)methylene)-2,5-dihydropyrrole). Dehydrogenation of PNP to dPNP results in minimal change to steric profile of the ligand but has important consequences for the resulting redox potentials of the metal complexes resulting in the ability to isolate both [CoH(tBudPNP)] and [CoEt(tBudPNP)], which are more challenging (hydride) or not possible (ethyl) to prepare with the parent PNP ligand. Electrochemical measurements with both the Co and Ni dPNP species demonstrate a substantial shift in redox potentials for both the M(II/III) and M(II/I) couples. In the case of the former, oxidation to trivalent Co was found to be reversible, and subsequent reaction with AgSbF6 afforded a rare example of a square-planar Co(III) species. Corresponding reduction of [CoCl(tBudPNP)] with KC8 produced the diamagnetic Co(I) species, [Co(N2)(tBudPNP)]. Further reduction of the Co(I) complex was found to generate a rare pincer-based π-radical anion that demonstrated well-resolved EPR features to the four hydrogen atoms and lone nitrogen atom of the ligand with minor contributions from cobalt and coordinated N2. Changes in the electronic character of the PNP ligand upon dehydrogenation are proposed to result from loss of aromaticity in the pyrrole ligand resulting in a more reducing central amido donor. DFT calculations on the Co(II) complexes were performed to shed further insight into the electronic structure of the pincer complexes.

Hemiprotonated dimers of cytosine derivatives, implicated in the formation of the i-motif of DNA, have been created in solution and the gas phase. The mechanism of dimerization has been analyzed by mass spectrometry and multidimensional NMR spectroscopy.