Arene C-H insertion catalyzed by ferrocene covalently heterogenized on graphene acid

被引:26
|
作者
Mosconi, Dario [1 ,2 ]
Blanco, Matias [1 ,2 ]
Gatti, Teresa [1 ,2 ]
Calvillo, Laura [1 ,2 ]
Otyepka, Michal [3 ]
Bakandritsos, Aristides [3 ]
Menna, Enzo [1 ,2 ]
Agnoli, Stefano [1 ,2 ]
Granozzi, Gaetano [1 ,2 ]
机构
[1] Univ Padua, Dept Chem Sci, Via F Marzolo 1, I-35131 Padua, Italy
[2] Univ Padua, INSTM Unit, Via F Marzolo 1, I-35131 Padua, Italy
[3] Palacky Univ Olomouc, Fac Sci, Dept Phys Chem, Reg Ctr Adv Technol & Mat, 17 Listopadu 1192-12, Olomouc 77146, Czech Republic
基金
欧盟地平线“2020”;
关键词
ONE-POT SYNTHESIS; ELECTRON-TRANSFER; HYBRID MATERIALS; OXIDE; FUNCTIONALIZATION; REDUCTION; CHEMISTRY; EFFICIENT; HYDROGENATION; ARYLATION;
D O I
10.1016/j.carbon.2018.11.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The heterogenation of molecular catalysts on solid supports is a viable route for the preparation of hybrid materials that combine the high selectivity and activity of homogeneous active species with the enhanced stability and recyclability imparted by the heterogeneous nature of the support. In this work we describe the covalent functionalization with ferrocene (Fc) of two graphene derivatives: graphene acid (GA), a graphene layer whose basal plane is modified with COOH groups, and graphene oxide (GO). The surface modification is performed exploiting the carbodiimide chemistry, which allows introducing up to 3.6% at. of iron in the GA-based material. Compared to GO, GA owns a superior functionalization degree, which is attributed to its controlled surface chemistry. Both Fc-modified materials are tested as catalysts in the CeH insertion of diazonium salts employing arene substrates. The materials are active, versatile and recyclable catalysts that show a catalytic performance comparable to or even better than molecular Fc, together with a 100% recyclability which does not alter the catalytic performance. The GAbased hybrid catalyst results more active than that based on GO due to the presence of more extended aromatic domains that facilitate the adsorption of the reagents close to the active sites. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:318 / 328
页数:11
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