Issue 13, 2022

Covalent organic frameworks anchored with frustrated Lewis pairs for hydrogenation of alkynes with H2

Abstract

Frustrated Lewis Pair (FLP) chemistry has been widely explored in the field of catalytic hydrogenation. However, FLPs, which are usually used as homogeneous catalysts, quickly lose their catalytic reactivity in the process of recycling due to their solubility and instability. Herein, we provide a solution to this issue by anchoring triaryl phosphorus used as the Lewis base of FLPs in two kinds of bromine functionalized covalent organic frameworks (COFs). Then, tris(pentafluorophenyl)boron (BCF) was introduced as the Lewis acid of FLPs, resulting in COF supported heterogeneous FLP catalysts, called COFs-FLPs which are the first COFs anchored with FLPs. These heterogeneous COFs-FLP catalysts show excellent catalytic reactivity for the hydrogenation of alkynes to olefins. More importantly, these COFs-FLPs can be easily re-cycled at least 10 times without losing their catalytic reactivity.

Graphical abstract: Covalent organic frameworks anchored with frustrated Lewis pairs for hydrogenation of alkynes with H2

Supplementary files

Article information

Article type
Paper
Submitted
18 Oct 2021
Accepted
09 Dec 2021
First published
10 Dec 2021

J. Mater. Chem. A, 2022,10, 7333-7340

Covalent organic frameworks anchored with frustrated Lewis pairs for hydrogenation of alkynes with H2

Q. Liu, Q. Liao, J. Hu, K. Xi, Y. Wu and X. Hu, J. Mater. Chem. A, 2022, 10, 7333 DOI: 10.1039/D1TA08916A

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