Gorgas Nikolaus, Stöger Berthold, Veiros Luis F, Kirchner Karl
Institute of Applied Synthetic Chemistry and Institute of Chemical Technologies and Analytics, Vienna University of Technology , Getreidemarkt 9, A-1060 Vienna, Austria.
Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa , Av. Rovisco Pais No. 1, 1049-001 Lisboa, Portugal.
ACS Catal. 2016 Apr 1;6(4):2664-2672. doi: 10.1021/acscatal.6b00436. Epub 2016 Mar 11.
The synthesis and application of [Fe(PNP-Pr)(CO)(H)(Br)] and [Fe(PNP-Pr)(H)(CO)] as catalysts for the homogeneous hydrogenation of aldehydes is described. These systems were found to be among the most efficient catalysts for this process reported to date and constitute rare examples of a catalytic process which allows selective reduction of aldehydes in the presence of ketones and other reducible functionalities. In some cases, TONs and TOFs of up to 80000 and 20000 h, respectively, were reached. On the basis of stoichiometric experiments and computational studies, a mechanism which proceeds via a -dihydride intermediate is proposed. The structure of the hydride complexes was also confirmed by X-ray crystallography.
本文描述了[Fe(PNP-Pr)(CO)(H)(Br)]和[Fe(PNP-Pr)(H)(CO)]作为醛类均相氢化催化剂的合成及应用。这些体系是迄今为止报道的该反应最有效的催化剂之一,也是在酮类和其他可还原官能团存在下能够选择性还原醛类的催化过程的罕见实例。在某些情况下,TON(总转化数)和TOF(转化频率)分别高达80000和20000 h⁻¹。基于化学计量实验和计算研究,提出了一种通过α-二氢化物中间体进行的反应机理。氢化物配合物的结构也通过X射线晶体学得到了证实。