Journalartikel

Jahr der Veröffentlichung: 2015

Seiten: 5332-5335

Zeitschrift: Journal of the American Chemical Society

Bandnummer: 137

Heftnummer: 16

ISSN: 0002-7863

DOI Link: https://doi.org/10.1021/jacs.5b02905

Verlag: American Chemical Society

Abstract: 
A new transition-metal-free mode for the catalytic reduction of carbon dioxide via bidentate interaction has been developed. In the presence of Li-2[1,2-C6H4(BH3)(2)], CO2 can be selectively transformed to either methane or methanol, depending on the reducing agent. The bidentate nature of binding is supported by X-ray analysis of an intermediate analogue, which experiences special stabilization due to aromatic character in the bidentate interaction. Kinetic studies revealed a first-order reaction rate. The transformation can be conducted without any solvent.

Harvard-Zitierstil: Lu, Z., Hausmann, H., Becker, S. and Wegner, H. (2015) Aromaticity as Stabilizing Element in the Bidentate Activation for the Catalytic Reduction of Carbon Dioxide, Journal of the American Chemical Society, 137(16), pp. 5332-5335. https://doi.org/10.1021/jacs.5b02905

APA-Zitierstil: Lu, Z., Hausmann, H., Becker, S., & Wegner, H. (2015). Aromaticity as Stabilizing Element in the Bidentate Activation for the Catalytic Reduction of Carbon Dioxide. Journal of the American Chemical Society. 137(16), 5332-5335. https://doi.org/10.1021/jacs.5b02905