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Ligand-Mediated Spin-State Changes in a Cobalt-Dipyrrin-Bisphenol Complex

[Image: see text] The influence of a redox-active ligand on spin-changing events induced by the coordination of exogenous donors is investigated within the cobalt complex [Co(II)(DPP·(2–))], bearing a redox-active DPP(2–) ligand (DPP = dipyrrin-bis(o,p-di-tert-butylphenolato) with a pentafluoropheny...

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Detalles Bibliográficos
Autores principales: van Leest, Nicolaas P., Stroek, Wowa, Siegler, Maxime A., van der Vlugt, Jarl Ivar, Bruin, Bas de
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482399/
https://www.ncbi.nlm.nih.gov/pubmed/32815718
http://dx.doi.org/10.1021/acs.inorgchem.0c01979
Descripción
Sumario:[Image: see text] The influence of a redox-active ligand on spin-changing events induced by the coordination of exogenous donors is investigated within the cobalt complex [Co(II)(DPP·(2–))], bearing a redox-active DPP(2–) ligand (DPP = dipyrrin-bis(o,p-di-tert-butylphenolato) with a pentafluorophenyl moiety on the meso-position. This square-planar complex was subjected to the coordination of tetrahydrofuran (THF), pyridine, tBuNH(2), and AdNH(2) (Ad = 1-adamantyl), and the resulting complexes were analyzed with a variety of experimental (X-ray diffraction, NMR, UV–visible, high-resolution mass spectrometry, superconducting quantum interference device, Evans’ method) and computational (density functional theory, NEVPT2-CASSCF) techniques to elucidate the respective structures, spin states, and orbital compositions of the corresponding octahedral bis-donor adducts, relative to [Co(II)(DPP·(2–))]. This starting species is best described as an open-shell singlet complex containing a DPP·(2–) ligand radical that is antiferromagnetically coupled to a low-spin (S = (1)/(2)) cobalt(II) center. The redox-active DPP(n–) ligand plays a crucial role in stabilizing this complex and in its facile conversion to the triplet THF adduct [Co(II)(DPP·(2–))(THF)(2)] and closed-shell singlet pyridine and amine adducts [Co(III)(DPP(3–))(L)(2)] (L = py, tBuNH(2), or AdNH(2)). Coordination of the weak donor THF to [Co(II)(DPP·(2–))] changes the orbital overlap between the DPP·(2–) ligand radical π-orbitals and the cobalt(II) metalloradical d-orbitals, which results in a spin-flip to the triplet ground state without changing the oxidation states of the metal or DPP·(2–) ligand. In contrast, coordination of the stronger donors pyridine, tBuNH(2), or AdNH(2) induces metal-to-ligand single-electron transfer, resulting in the formation of low-spin (S = 0) cobalt(III) complexes [Co(III)(DPP(3–))(L)(2)] containing a fully reduced DPP(3–) ligand, thus explaining their closed-shell singlet electronic ground states.