Journal article
Authors list: Lu, ZP; Hausmann, H; Becker, S; Wegner, HA
Publication year: 2015
Pages: 5332-5335
Journal: Journal of the American Chemical Society
Volume number: 137
Issue number: 16
ISSN: 0002-7863
DOI Link: https://doi.org/10.1021/jacs.5b02905
Publisher: 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.
Citation Styles
Harvard Citation style: 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 Citation style: 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