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铱氮杂环卡宾配合物催化甲醇脱氢反应

Methanol dehydrogenation by iridium N-heterocyclic carbene complexes.

作者信息

Campos Jesús, Sharninghausen Liam S, Manas Michael G, Crabtree Robert H

机构信息

Chemistry Department, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.

出版信息

Inorg Chem. 2015 Jun 1;54(11):5079-84. doi: 10.1021/ic502521c. Epub 2015 Jan 23.

Abstract

A series of homogeneous iridium bis(N-heterocyclic carbene) catalysts are active for three transformations involving dehydrogenative methanol activation: acceptorless dehydrogenation, transfer hydrogenation, and amine monoalkylation. The acceptorless dehydrogenation reaction requires base, yielding formate and carbonate, as well as 2-3 equivalents of H2. Of the few homogeneous systems known for this reaction, our catalysts tolerate air and employ simple ligands. Transfer hydrogenation of ketones and imines from methanol is also possible. Finally, N-monomethylation of anilines occurs through a "borrowing hydrogen" reaction. Notably, this reaction is highly selective for the monomethylated product.

摘要

一系列均相铱双(N - 杂环卡宾)催化剂对涉及脱氢甲醇活化的三种转化反应具有活性:无受体脱氢、转移氢化和胺单烷基化。无受体脱氢反应需要碱,生成甲酸盐和碳酸盐以及2 - 3当量的氢气。在已知的用于该反应的少数均相体系中,我们的催化剂能耐受空气并使用简单的配体。酮和亚胺从甲醇进行转移氢化也是可行的。最后,苯胺的N - 单甲基化通过“借氢”反应发生。值得注意的是,该反应对单甲基化产物具有高度选择性。

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