Issue 1, 2014

Preparation of bifunctionalized phenylene-bridged periodic mesoporous organosilica for solid-phase microextraction

Abstract

Well-ordered bifunctionalized periodic mesoporous organosilicas (BPMOs), with various mesostructures (like hexagonal p6mm, cubic Ia[3 with combining macron]d symmetry), relatively large mesopores, a phenylene-bridged skeleton and vinyl functional groups, were first prepared by co-condensation of 1,4-bis(triethoxysilyl)benzene (BTEB) and triethoxyvinylsilane (TEVS) with a triblock copolymer (P123) as a template under acid conditions. It was found that the mesostructure of the BPMOs can be facilely tuned by altering the fraction of organosilanes in the synthesis mixture. With an increase of TEVS content, the mesostructure changed from p6mm to Ia[3 with combining macron]d, until disordered. The mechanisms of the mesophase transformation were discussed based on the adsorption of vinyl groups into the micelles and the relative reactivities of the organosilane precursors. In addition, the potential application of the BPMOs as an effective fibre-coating absorbent is tested in solid-phase microextraction (SPME) analyses.

Graphical abstract: Preparation of bifunctionalized phenylene-bridged periodic mesoporous organosilica for solid-phase microextraction

Supplementary files

Article information

Article type
Paper
Submitted
01 Sep 2013
Accepted
30 Oct 2013
First published
30 Oct 2013

RSC Adv., 2014,4, 168-174

Preparation of bifunctionalized phenylene-bridged periodic mesoporous organosilica for solid-phase microextraction

L. Y. Xia, Y. C. Hu, M. Z. Rong and Y. J. Liang, RSC Adv., 2014, 4, 168 DOI: 10.1039/C3RA46178E

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