Issue 7, 2018

A single palladium site catalyst as a bridge for converting homogeneous to heterogeneous in dimerization of terminal aryl acetylenes

Abstract

Herein, we utilize the surface dangling bond of MOFs as anchoring sites to access single Pd sites embedded on a hollow MOF nanobox. The stabilization of isolated Pd1 species is based on the strong coordination of the surface dangling bond of MOFs, followed by sequential reduction and phase transfer processes. The supported isolated single Pd sites can effect the highly active and selective process to produce conjugated dienes towards the dimerization of terminal aryl acetylenes, which has been previously only catalyzed by homogeneous catalysts. Unlike the commercial Pd/C and nanoparticles (NPs), the heterolytic cleavage of H2 and C–H bond efficient cleavage of terminal alkynes on atomically dispersed Pd1 sites ensure the high selectivity process and prevent the generation of styrene.

Graphical abstract: A single palladium site catalyst as a bridge for converting homogeneous to heterogeneous in dimerization of terminal aryl acetylenes

Supplementary files

Article information

Article type
Research Article
Submitted
07 Mär 2018
Accepted
25 Mär 2018
First published
27 Mär 2018

Mater. Chem. Front., 2018,2, 1317-1322

A single palladium site catalyst as a bridge for converting homogeneous to heterogeneous in dimerization of terminal aryl acetylenes

C. Zhao, H. Yu, J. Wang, W. Che, Z. Li, T. Yao, W. Yan, M. Chen, J. Yang, S. Wei, Y. Wu and Y. Li, Mater. Chem. Front., 2018, 2, 1317 DOI: 10.1039/C8QM00095F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements