Issue 20, 2014

Amine-functionalized metal-organic frameworks for the transesterification of triglycerides

Abstract

For the application of functionalized metal–organic frameworks (MOFs) as a solid base, amine-functionalized MOF materials are achieved by (i) dative modification of unsaturated metal sites located at the secondary building units of MOFs with diamine, and (ii) covalent modification of the amine-tagged organic linkers within the MOF by alkylation with 2-dimethylaminoethyl chloride. The resulting amine-functionalized MOFs exhibit excellent results in the liquid phase transesterification of triglycerides and methanol, with the triglyceride conversions exceeding 99%, which are important model reactions for the production of biodiesel. The relationship between the catalytic activity towards transesterification and the basicity of amine-functionalized MOFs reveals a linear correspondence in terms of turnover frequency and basic site density. The basicity of the MOFs and reaction parameters are shown to significantly affect the catalytic performance. Kinetics studies reveal that the reaction follows first-order kinetics with the calculated activation energy of 48.2 kJ mol−1. This research opens up new perspectives on the postsynthetic modification of MOFs and more generally on the rational design of MOF-derived solid base catalysts.

Graphical abstract: Amine-functionalized metal-organic frameworks for the transesterification of triglycerides

Supplementary files

Article information

Article type
Paper
Submitted
16 Jan 2014
Accepted
19 Feb 2014
First published
19 Feb 2014

J. Mater. Chem. A, 2014,2, 7205-7213

Author version available

Amine-functionalized metal-organic frameworks for the transesterification of triglycerides

J. Chen, R. Liu, H. Gao, L. Chen and D. Ye, J. Mater. Chem. A, 2014, 2, 7205 DOI: 10.1039/C4TA00253A

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