Organized thiol functional groups in mesoporous core shell colloids

The co-condensation in situ of tetraethoxysilane (TEOS) and mercaptopropyltrimethoxysilane (MPTMS) using cetyltrimethylammonium bromide (CTAB) as a template results in the synthesis of multilayered mesoporous structured SiO2 colloids with “onion-like” chemical environments. Thiol groups were anchore...

Full description

Saved in:
Bibliographic Details
Published inJournal of solid state chemistry Vol. 187; pp. 97 - 102
Main Authors Marchena, Martín H., Granada, Mara, Bordoni, Andrea V., Joselevich, María, Troiani, Horacio, Williams, Federico J., Wolosiuk, Alejandro
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.03.2012
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The co-condensation in situ of tetraethoxysilane (TEOS) and mercaptopropyltrimethoxysilane (MPTMS) using cetyltrimethylammonium bromide (CTAB) as a template results in the synthesis of multilayered mesoporous structured SiO2 colloids with “onion-like” chemical environments. Thiol groups were anchored to an inner selected SiO2 porous layer in a bilayered core shell particle producing different chemical regions inside the colloidal layered structure. X-Ray Photoelectron Spectroscopy (XPS) shows a preferential anchoring of the –SH groups in the double layer shell system, while porosimetry and simple chemical modifications confirm that pores are accessible. We can envision the synthesis of interesting colloidal objects with defined chemical environments with highly controlled properties. Mesoporous core shell SiO2 colloids with organized thiol groups. [Display omitted] ► Double shell mesoporous silica colloids templated with CTAB. ► Sequential deposition of mesoporous SiO2 layers with different chemistries. ► XPS shows the selective functionalization of mesoporous layers with thiol groups.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0022-4596
1095-726X
DOI:10.1016/j.jssc.2011.12.028