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本文引用的文献

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Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.用于醇无受体脱氢制羧酸的铱催化剂:范围与机理
ACS Catal. 2018 May 4;8(5):3754-3763. doi: 10.1021/acscatal.8b00105. Epub 2018 Mar 26.
2
Dehydrogenation of formic acid by Ir-bisMETAMORPhos complexes: experimental and computational insight into the role of a cooperative ligand.铱-双METAMORPhos配合物催化甲酸脱氢反应:对协同配体作用的实验与计算研究
Chem Sci. 2015 Feb 1;6(2):1027-1034. doi: 10.1039/c4sc02555e. Epub 2014 Oct 22.
3
Ruthenium PNN(O) Complexes: Cooperative Reactivity and Application as Catalysts for Acceptorless Dehydrogenative Coupling Reactions.钌PNN(O)配合物:协同反应性及作为无受体脱氢偶联反应催化剂的应用
Organometallics. 2017 Apr 24;36(8):1541-1549. doi: 10.1021/acs.organomet.7b00111. Epub 2017 Apr 6.
4
Iron-based nanocatalyst for the acceptorless dehydrogenation reactions.用于受体非依赖性脱氢反应的铁基纳米催化剂。
Nat Commun. 2017 Dec 15;8(1):2147. doi: 10.1038/s41467-017-01603-3.
5
Protic NNN and NCN Pincer-Type Ruthenium Complexes Featuring (Trifluoromethyl)pyrazole Arms: Synthesis and Application to Catalytic Hydrogen Evolution from Formic Acid.含(三氟甲基)吡唑臂的质子型NNN和NCN钳形钌配合物:合成及其在甲酸催化析氢中的应用
Chem Asian J. 2018 Jan 4;13(1):73-80. doi: 10.1002/asia.201701474. Epub 2017 Dec 5.
6
Manganese Complexes for (De)Hydrogenation Catalysis: A Comparison to Cobalt and Iron Catalysts.锰配合物在(脱氢)氢化催化中的应用:与钴和铁催化剂的比较。
Angew Chem Int Ed Engl. 2018 Jan 2;57(1):46-60. doi: 10.1002/anie.201709010. Epub 2017 Dec 8.
7
Ligand Substituents Govern the Efficiency and Mechanistic Path of Hydrogen Production with [Cp*Rh] Catalysts.配体取代基调控[Cp*Rh]催化剂产氢的效率和反应机理。
ChemSusChem. 2017 Nov 23;10(22):4589-4598. doi: 10.1002/cssc.201701416. Epub 2017 Nov 2.
8
Homogeneous Catalysis for Sustainable Hydrogen Storage in Formic Acid and Alcohols.甲酸和醇中可持续储氢的均相催化
Chem Rev. 2018 Jan 24;118(2):372-433. doi: 10.1021/acs.chemrev.7b00182. Epub 2017 Oct 6.
9
Dehydrogenation of Alkanes and Aliphatic Groups by Pincer-Ligated Metal Complexes.钳式配体金属配合物促进的烷烃和脂肪族基团的脱氢反应。
Chem Rev. 2017 Oct 11;117(19):12357-12384. doi: 10.1021/acs.chemrev.7b00247. Epub 2017 Sep 27.
10
Reversible Interconversion between 2,5-Dimethylpyrazine and 2,5-Dimethylpiperazine by Iridium-Catalyzed Hydrogenation/Dehydrogenation for Efficient Hydrogen Storage.铱催化加氢/脱氢实现 2,5-二甲基吡嗪和 2,5-二甲基哌嗪的可逆互变用于高效储氢。
Angew Chem Int Ed Engl. 2017 Aug 28;56(36):10886-10889. doi: 10.1002/anie.201705452. Epub 2017 Jul 27.

基于铱的氢化物转移催化剂:从储氢到精细化学品。

Iridium-based hydride transfer catalysts: from hydrogen storage to fine chemicals.

机构信息

Loker Hydrocarbon Research Institute and Department of Chemistry, University of Southern California, 837 Bloom Walk, Los Angeles, CA 90089-1661, USA.

出版信息

Chem Commun (Camb). 2018 Jul 10;54(56):7711-7724. doi: 10.1039/c8cc03412e.

DOI:10.1039/c8cc03412e
PMID:29888372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6039230/
Abstract

Selective hydrogen transfer remains a central research focus in catalysis: hydrogenation and dehydrogenation have central roles, both historical and contemporary, in all aspects of fuel, agricultural, pharmaceutical, and fine chemical synthesis. Our lab has been involved in this area by designing homogeneous catalysts for dehydrogenation and hydrogen transfer that fill needs ranging from on-demand hydrogen storage to fine chemical synthesis. A keen eye toward mechanism has enabled us to develop systems with excellent selectivity and longevity and demonstrate these in a diversity of high-value applications. Here we describe recent work from our lab in these areas that are linked by a central mechanistic trichotomy of catalyst initiation pathways that lead highly analogous precursors to a diversity of useful applications.

摘要

选择性氢转移仍然是催化研究的核心关注点

加氢和脱氢在燃料、农业、制药和精细化学品合成的各个方面都具有历史和当代的核心作用。我们的实验室通过设计用于脱氢和氢转移的均相催化剂参与了这一领域,这些催化剂满足了从按需储氢到精细化学品合成等各种需求。对反应机制的敏锐观察使我们能够开发出具有优异选择性和长寿命的系统,并在各种高价值应用中展示这些系统。在这里,我们描述了我们实验室在这些领域的最新工作,这些工作通过催化剂引发途径的中心机制三分法联系在一起,这些途径导致高度类似的前体转化为多种有用的应用。

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