A Singlet Biradicaloid Zinc Compound and Its Nonradical Counterpart.

Metal ions with radical centers in their coordination sphere are key participants in biological and catalytic processes. In the present study, we describe the synthesis of the cAAC:ZnCl adduct (1) using a cyclic alkylaminocarbene (cAAC) as donor ligand. Compound 1 was treated with 2 equiv of KC and...

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Detalles Bibliográficos
Publicado en:Journal of the American Chemical Society Vol. 135; no. 19; pp. 7324 - 7330
Autores principales: Pratap Singh, Amit, Samuel, Prinson P., Roesky, Herbert W., Schwarzer, Martin C., Frenking, Gernot, Sidhu, Navdeep S., Dittrich, Birger
Formato: Artículo
Publicado: American Chemical Society 5/15/2013
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Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Metal ions with radical centers in their coordination sphere are key participants in biological and catalytic processes. In the present study, we describe the synthesis of the cAAC:ZnCl adduct (1) using a cyclic alkylaminocarbene (cAAC) as donor ligand. Compound 1 was treated with 2 equiv of KC and LiB(sec-Bu)H to yield a deep blue-colored dicarbene zinc compound (cAAC)Zn (2) and the colorless hydrogenated zinc compound (cAACH)Zn (3), respectively. Compounds 2 and 3 were well characterized by spectroscopic methods and single-crystal X-ray structural analysis. Density functional theory calculations were performed for 2 which indicate that this molecule possesses a singlet biradicaloid character. Moreover, we show the application of 2 in CO activation, which yields a zwitterionic cAAC·CO adduct.