Issue 55, 2015

Catalytic cleavage of C–O linkages in benzyl phenyl ether assisted by microwave heating

Abstract

The microwave-assisted cleavage of C–O linkages in benzyl phenyl ether was investigated at 200 °C in the presence of ZrP or SBA-15 doped with or without metal catalyst (Pd/C or Ru/C). The total yield of phenol and benzyl alcohol from benzyl phenyl ether depolymerization with ZrP was 26.91%, while the yield of phenol reached 26.11% for that with Pd/C. Hybrid catalysts performed effectively for promoting the formation of phenol. A conversion of 85.70% was achieved with ZrP–Pd/C catalyst, and the selectivity to phenol reached 47.32%. The highest yield of phenol was obtained at 1 h, and repolymerization was remarkable at longer reaction time. Based on the reaction using phenol and benzyl alcohol as the reactants, benzyl phenyl ether might be decomposed into phenol and benzyl alcohol following with the repolymerization producing thermally stable polymers in the presence of Pd.

Graphical abstract: Catalytic cleavage of C–O linkages in benzyl phenyl ether assisted by microwave heating

Supplementary files

Article information

Article type
Paper
Submitted
20 Mar 2015
Accepted
11 May 2015
First published
11 May 2015

RSC Adv., 2015,5, 43972-43977

Author version available

Catalytic cleavage of C–O linkages in benzyl phenyl ether assisted by microwave heating

J. Hu, D. Shen, S. Wu, H. Zhang and R. Xiao, RSC Adv., 2015, 5, 43972 DOI: 10.1039/C5RA04974A

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