Unveiling the Local Structure of Palladium Loaded into Imine-Linked Layered Covalent Organic Frameworks for Cross-Coupling Catalysis

被引:66
|
作者
Romero-Muniz, Ignacio [1 ]
Mavrandonakis, Andreas [2 ]
Albacete, Pablo [1 ]
Vega, Alicia [1 ]
Briois, Valerie [3 ]
Zamora, Felix [1 ,4 ,5 ]
Platero-Prats, Ana E. [1 ,4 ]
机构
[1] Univ Autonoma Madrid, Dept Quim Inorg, Fac Ciencias, Campus Cantoblanco, E-28049 Madrid, Spain
[2] IMDEA Energy, Elect Proc Unit, Ave Ramon de la Sagra 3, Madrid 28935, Spain
[3] LOrme Merisiers, Synchrotron SOLEIL, BP48, F-91192 Gif Sur Yvette, France
[4] Univ Autonoma Madrid, Condensed Matter Phys Ctr IFIMAC, Campus Cantoblanco, E-28049 Madrid, Spain
[5] Univ Autonoma Madrid, Inst Invest Avanzada Ciencias Quim, Campus Cantoblanco, E-28049 Madrid, Spain
基金
欧盟地平线“2020”;
关键词
cross-coupling catalysis; DFT modeling; layered covalent organic frameworks; pair distribution function; NANOPARTICLES; CONSTRUCTION;
D O I
10.1002/anie.202004197
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Layered covalent organic frameworks (2D-COFs), composed of reversible imine linkages and accessible pores, offer versatility for chemical modifications towards the development of catalytic materials. Nitrogen-enriched COFs are good candidates for binding Pd species. Understanding the local structure of reacting Pd sites bonded to the COF pores is key to rationalize interactions between active sites and porous surfaces. By combining advanced synchrotron characterization methods with periodic computational DFT modeling, the precise atomic structure of catalytic Pd sites attached to local defects is resolved within an archetypical imine-linked 2D-COF. This material was synthesized using an in situ method as a gel, under which imine hydrolysis and metalation reactions are coupled. Local defects formed in situ within imine-linked 2D-COF materials are highly reactive towards Pd metalation, resulting in active materials for Suzuki-Miyaura cross-coupling reactions.
引用
收藏
页码:13013 / 13020
页数:8
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