Synthesis of mesostructured silica from monoalkyl-substituted double five-ring units

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Abstract

A mesostructured silica-based material was synthesized by self-assembly of a novel amphiphilic molecule consisting of a well-defined siloxane head with a double five-ring (D5R) structure and a hydrophobic alkyl tail. A precursor functionalized with ethoxy groups, C22H45Si 10O15(OEt)9 (1), was hydrolyzed under an acidic condition with the retention of the D5R units, leading to the formation of two-dimensional (2D) hexagonal phase by evaporation-induced self-assembly of amphiphilic hydrolyzed molecules. Solid-state 29Si MAS NMR analysis of the resulting hybrid solid confirmed that the D5R units were cross-linked to form siloxane networks. Calcination of this hybrid solid gave mesoporous silica with high BET surface area (740 m2 g-1). These results expand the design possibility of silica-based materials at both molecular- and meso-scales, leading to the bottom up synthesis of hierarchically ordered materials.

Original languageEnglish
Pages (from-to)263-268
Number of pages6
JournalJournal of Sol-Gel Science and Technology
Volume57
Issue number3
DOIs
Publication statusPublished - 2011 Mar 1

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Keywords

  • Mesoporous silica
  • Organic-inorganic hybrid
  • Self-assembly
  • Siloxane cage

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Biomaterials
  • Condensed Matter Physics
  • Materials Chemistry

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