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源自功能化石墨烯的混合价态单原子催化剂。

Mixed-Valence Single-Atom Catalyst Derived from Functionalized Graphene.

作者信息

Bakandritsos Aristides, Kadam Ravishankar G, Kumar Pawan, Zoppellaro Giorgio, Medved' Miroslav, Tuček Jiří, Montini Tiziano, Tomanec Ondřej, Andrýsková Pavlína, Drahoš Bohuslav, Varma Rajender S, Otyepka Michal, Gawande Manoj B, Fornasiero Paolo, Zbořil Radek

机构信息

Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University Olomouc, Šlechtitelu˚ 27, 783 71, Olomouc, Czech Republic.

Department of Chemical and Pharmaceutical Sciences, INSTM Trieste Research Unit and ICCOM-CNR Trieste Research Unit, University of Trieste, via L. Giorgieri 1, I-34127, Trieste, Italy.

出版信息

Adv Mater. 2019 Apr;31(17):e1900323. doi: 10.1002/adma.201900323. Epub 2019 Feb 27.

Abstract

Single-atom catalysts (SACs) aim at bridging the gap between homogeneous and heterogeneous catalysis. The challenge is the development of materials with ligands enabling coordination of metal atoms in different valence states, and preventing leaching or nanoparticle formation. Graphene functionalized with nitrile groups (cyanographene) is herein employed for the robust coordination of Cu(II) ions, which are partially reduced to Cu(I) due to graphene-induced charge transfer. Inspired by nature's selection of Cu(I) in enzymes for oxygen activation, this 2D mixed-valence SAC performs flawlessly in two O -mediated reactions: the oxidative coupling of amines and the oxidation of benzylic CH bonds toward high-value pharmaceutical synthons. High conversions (up to 98%), selectivities (up to 99%), and recyclability are attained with very low metal loadings in the reaction. The synergistic effect of Cu(II) and Cu(I) is the essential part in the reaction mechanism. The developed strategy opens the door to a broad portfolio of other SACs via their coordination to various functional groups of graphene, as demonstrated by successful entrapment of Fe /Fe single atoms to carboxy-graphene.

摘要

单原子催化剂(SACs)旨在弥合均相催化和多相催化之间的差距。挑战在于开发具有配体的材料,以使金属原子能够以不同价态配位,并防止浸出或纳米颗粒形成。本文采用腈基功能化的石墨烯(氰基石墨烯)来实现Cu(II)离子的牢固配位,由于石墨烯诱导的电荷转移,Cu(II)离子会部分还原为Cu(I)。受自然界中酶选择Cu(I)进行氧活化的启发,这种二维混合价态SAC在两个O介导的反应中表现完美:胺的氧化偶联和苄基C-H键向高价值药物合成子的氧化。在反应中使用非常低的金属负载量即可实现高转化率(高达98%)、高选择性(高达99%)和可回收性。Cu(II)和Cu(I)的协同作用是反应机理的关键部分。所开发的策略为通过与石墨烯的各种官能团配位来制备其他多种SAC打开了大门,成功将Fe/Fe单原子捕获到羧基石墨烯中就证明了这一点。

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