Tying Covalent Organic Frameworks through Alkene Metathesis and Supported Platinum as Efficient Catalysts for Hydrosilylation

Nanomaterials

Guangwen Li¹  Yuzhou Liu²  Defa Gu²  Yushan Liu³ 

[1] Research Institute of Petroleum Processing, SINOPEC, Beijing 100083, China;School of Chemistry, Beihang University, Bejing 100191, China;Trinity School of Durham and Chapel Hill, Durham, NC 27705, USA;

关键词: hydrolytic stability;    hierarchical bond formation;    alkene metathesis;    hydrosilylation;   

DOI  :  10.3390/nano12030499

来源: DOAJ

【 摘 要 】

Recently there has been a great interest in covalent organic frameworks due to their fascinating properties. Current approaches to improve their hydrolytic stability mainly rely on the transformation of the dynamic bonds into strong and irreversible bonds, but these approaches also reduce the versatility of the frameworks. Herein, we would like to demonstrate a solution to this dilemma by forming hierarchical bonds through olefin metathesis to produce highly stable COFs. Our approach allows unprecedented opportunities for post-modification of the inner space through the dynamic imine bonds while maintaining the integrity of the framework. Specifically, we demonstrate an amorphous-to-crystalline transformation. In addition, the porosity can be enhanced by up to 70% after full removal of the amine subunits. Overall, our work provides a new direction for the generation of highly stable while still versatile COFs. Meanwhile, platinum(II) complexes can be supported on BHU-2 (Pt@BHU-2) or BHU-2-Oxidate(Pt@BHU-2-Oxidate) as efficient catalysts for hydrosilylation.

【 授权许可】

Unknown