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Microsecond Photoluminescence and Photoreactivity of a Metal-Centered Excited State in a Hexacarbene–Co(III) Complex

[Image: see text] The photofunctionality of the cobalt–hexacarbene complex [Co(III)(PhB(MeIm)(3))(2)](+) (PhB(MeIm)(3) = tris(3-methylimidazolin-2-ylidene)(phenyl)borate) has been investigated by time-resolved optical spectroscopy. The complex displays a weak (Φ ∼ 10(–4)) but remarkably long-lived (...

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Detalles Bibliográficos
Autores principales: Kaufhold, Simon, Rosemann, Nils W., Chábera, Pavel, Lindh, Linnea, Bolaño Losada, Iria, Uhlig, Jens, Pascher, Torbjörn, Strand, Daniel, Wärnmark, Kenneth, Yartsev, Arkady, Persson, Petter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877722/
https://www.ncbi.nlm.nih.gov/pubmed/33449685
http://dx.doi.org/10.1021/jacs.0c12151
Descripción
Sumario:[Image: see text] The photofunctionality of the cobalt–hexacarbene complex [Co(III)(PhB(MeIm)(3))(2)](+) (PhB(MeIm)(3) = tris(3-methylimidazolin-2-ylidene)(phenyl)borate) has been investigated by time-resolved optical spectroscopy. The complex displays a weak (Φ ∼ 10(–4)) but remarkably long-lived (τ ∼ 1 μs) orange photoluminescence at 690 nm in solution at room temperature following excitation with wavelengths shorter than 350 nm. The strongly red-shifted emission is assigned from the spectroscopic evidence and quantum chemical calculations as a rare case of luminescence from a metal-centered state in a 3d(6) complex. Singlet oxygen quenching supports the assignment of the emitting state as a triplet metal-centered state and underlines its capability of driving excitation energy transfer processes.