Freitag Frederik, Irrgang Torsten, Kempe Rhett
Anorganische Chemie II-Katalysatordesign, Universität Bayreuth, 95540, Bayreuth, Germany.
Chemistry. 2017 Sep 7;23(50):12110-12113. doi: 10.1002/chem.201701211. Epub 2017 May 19.
Alcohols are promising sustainable starting materials because they can be obtained from abundant and indigestible biomass. The substitution of expensive noble metals in catalysis by earth abundant 3d metals, such as Mn, Fe, or Co, (nonprecious or base metals) is a related key concept with respect to sustainability. Here, we report on the first cobalt-catalyzed alkylation of secondary alcohols with primary alcohols. Easy-to-synthesize and easy-to-activate PN P-pincer-ligand-stabilized Co complexes developed in our laboratory mediate the reaction most efficiently. The catalysis is applicable to a broad substrate scope and proceeds under relatively mild conditions. We have even demonstrated the coupling of a variety of purely aliphatic alcohols with a base or nonprecious metal catalyst. Mechanistic studies indicate that the reaction follows the borrowing hydrogen or hydrogen autotransfer concept.
醇类是很有前景的可持续起始原料,因为它们可以从丰富且不可消化的生物质中获得。在催化过程中用储量丰富的3d金属(如锰、铁或钴,即非贵金属或贱金属)替代昂贵的贵金属是与可持续性相关的一个关键概念。在此,我们报道首例钴催化仲醇与伯醇的烷基化反应。我们实验室开发的易于合成且易于活化的PNP钳形配体稳定的钴配合物能最有效地介导该反应。该催化反应适用于广泛的底物范围,且在相对温和的条件下进行。我们甚至已经证明了各种纯脂肪族醇与碱或非贵金属催化剂的偶联反应。机理研究表明该反应遵循借氢或氢自转移概念。