journal article·2018-10-23Open access

Strategies for Localizing Multiple Functional Groups in Mesoporous Silica Particles through a One-Pot Synthesis

Nicola Zucchetto, Dominik Brühwiler

Chemistry of Materials· Volume 30· Issue 20

Abstract

The process of postcondensation for the functionalization of mesoporous silica is based on the cooperation between the end-on growth of arrays of silica nanochannels and the steric hindrance of the functional silanes (R-silanes). To obtain particles with differently functionalized surfaces (thiol and amino groups), the delayed addition of another R-silane was introduced. This tandem postcondensation approach allows for three selective functionalization strategies, depending on the mobility and the steric hindrance of the R-silanes. Following these one-pot synthesis strategies, functional groups can be placed independently on the pore entrances and on the internal surface of the mesoporous silica particles. Confocal laser scanning microscopy was used to image the functional group distribution after selective coupling with a fluorescent dye. Nitrogen sorption measurements were conducted to confirm the well-defined mesoporosity of the functionalized products.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Mesoporous Materials and Catalysis · Analytical Chemistry and Sensors · Diatoms and Algae Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of Chemistry and Biotechnology, Zürich University of Applied Sciences (ZHAW), CH-8820 Wädenswil, Switzerland

Funding

Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung

References (35)

Show source-provided references
1. 10.1021/ja00053a02010.1021/ja00053a020 ↗
2. 10.1021/nn200365a10.1021/nn200365a ↗
3. 10.1021/acs.chemmater.8b0187310.1021/acs.chemmater.8b01873 ↗
4. 10.1039/c0nr00039f10.1039/c0nr00039f ↗
5. 10.1021/nn405092w10.1021/nn405092w ↗
6. 10.1039/C5NR09112H10.1039/C5NR09112H ↗
7. 10.1002/chem.20150057810.1002/chem.201500578 ↗
8. 10.1016/j.jcat.2004.11.00810.1016/j.jcat.2004.11.008 ↗
9. 10.1039/C6BM00872K10.1039/C6BM00872K ↗
10. 10.1002/adhm.20120032610.1002/adhm.201200326 ↗
11. 10.1039/C6TB01468B10.1039/C6TB01468B ↗
12. 10.1016/j.micromeso.2017.03.05010.1016/j.micromeso.2017.03.050 ↗
13. 10.1016/j.colsurfb.2015.04.06810.1016/j.colsurfb.2015.04.068 ↗
14. 10.1016/j.chroma.2017.02.01210.1016/j.chroma.2017.02.012 ↗
15. 10.1166/jnn.2005.08910.1166/jnn.2005.089 ↗
16. 10.1002/anie.20050307510.1002/anie.200503075 ↗
17. 10.1016/S0927-7757(03)00138-910.1016/S0927-7757(03)00138-9 ↗
18. 10.1021/acs.chemmater.6b0362910.1021/acs.chemmater.6b03629 ↗
19. 10.1039/C6DT02033J10.1039/C6DT02033J ↗
20. 10.1021/jp048516i10.1021/jp048516i ↗
21. 10.1002/anie.20150474510.1002/anie.201504745 ↗
22. 10.1002/anie.20030057010.1002/anie.200300570 ↗
23. 10.1002/chem.20150440410.1002/chem.201504404 ↗
24. 10.1039/C5RA16913E10.1039/C5RA16913E ↗
25. 10.1002/anie.20090243610.1002/anie.200902436 ↗
26. 10.1515/pac-2014-111710.1515/pac-2014-1117 ↗
27. 10.1016/S1387-1811(01)00251-710.1016/S1387-1811(01)00251-7 ↗
28. 10.1021/ja01269a02310.1021/ja01269a023 ↗
29. 10.1109/TNANO.2005.85142510.1109/TNANO.2005.851425 ↗
30. 10.1038/386692a010.1038/386692a0 ↗
31. 10.1016/S0167-2991(98)80985-310.1016/S0167-2991(98)80985-3 ↗
32. 10.1021/acs.chemmater.7b0347210.1021/acs.chemmater.7b03472 ↗
33. 10.1039/c2cs15308d10.1039/c2cs15308d ↗
34. 10.1002/open.20150005310.1002/open.201500053 ↗
35. 10.1039/c0jm00645a10.1039/c0jm00645a ↗