Kalra S, Pividori DM, Fehn D, Dai C, Dong S, Yao S, Zhu J, Meyer K, Driess M (2022)
Publication Type: Journal article
Publication year: 2022
DOI: 10.1039/d2sc03352f
Using the potentially tridentate N,N'-bis(N-heterocyclic silylene)pyridine [SiNSi] pincer-type ligand, 2,6-N,N'-diethyl-bis[N,N'-di-tert-butyl(phenylamidinato)silylene] diaminopyridine, led to the first isolable bis(silylene)pyridine-stabilized manganese(0) complex, {kappa(3)-[SiNSi]Mn(dmpe)} 4 (dmpe = (Me2P)(2)C2H4), which represents an isolobal 17 VE analogue of the elusive Mn(CO)(5) radical. The compound is accessible through the reductive dehalogenation of the corresponding dihalido (SiNSi)Mn(II) complexes 1 (Cl) and 2 (Br) with potassium graphite. Exposing 4 towards the stronger pi-acceptor ligands CO and 2,6-dimethylphenyl isocyanide afforded the related Mn(0) complexes kappa(2)-[SiNSi]Mn(CO)(3) (5) and kappa(3)-[SiNSi] Mn(CNXylyl)(2)(kappa(1)-dmpe) (6), respectively. Remarkably, the stabilization of Mn(0) in the coordination sphere of the [SiNSi] ligand favors the d(7) low-spin electronic configuration, as suggested by EPR spectroscopy, SQUID measurements and DFT calculations. The suitability of 4 acting as a superior pre-catalyst in regioselective hydroboration of quinolines has also been demonstrated.
APA:
Kalra, S., Pividori, D.M., Fehn, D., Dai, C., Dong, S., Yao, S.,... Driess, M. (2022). A bis(silylene)pyridine pincer ligand can stabilize mononuclear manganese(0) complexes: facile access to isolable analogues of the elusive d(7)-Mn(CO)(5) radical. Chemical Science. https://doi.org/10.1039/d2sc03352f
MLA:
Kalra, Shweta, et al. "A bis(silylene)pyridine pincer ligand can stabilize mononuclear manganese(0) complexes: facile access to isolable analogues of the elusive d(7)-Mn(CO)(5) radical." Chemical Science (2022).
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