Efficient way to attach organosilyl groups in the interlayer space of layered solids

Yusuke Ide, Makoto Ogawa

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

An efficient method to immobilize silane-coupling reagents on the interlayer space of a layered silicate, magadiite (Na2Si 14O29 ·nH2O), is reported. The silylation was conducted by concentrating a mixture containing the pre-synthesized dodecyltrimethylammonium-exchanged magadiite and a stoichiometric amount (molar ratio of silane-coupling reagent/Si 14O29 unit of magadiite = 2.0) of (3-mercaptopropyl) trimethoxysilane. The resulting silylated derivative possessed basal spacing and had a composition comparable to those of the silylated derivative, prepared by using a previous silylation method, which involves dodecyltrimethylammonium- exchanged form with a much larger amount (molar ratio of silane-coupling reagent/Si14O29 unit of magadiite = 57) of the silane-coupling reagent. When the present method was employed, the surface coverage with (3-mercaptopropyl)silyl groups on the layer surface directly correlated to the amount of the silane-coupling reagent.

Original languageEnglish
Pages (from-to)1624-1629
Number of pages6
JournalBulletin of the Chemical Society of Japan
Volume80
Issue number8
DOIs
Publication statusPublished - 2007

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Silanes
Derivatives
Silicates
Chemical analysis

ASJC Scopus subject areas

  • Chemistry(all)

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Efficient way to attach organosilyl groups in the interlayer space of layered solids. / Ide, Yusuke; Ogawa, Makoto.

In: Bulletin of the Chemical Society of Japan, Vol. 80, No. 8, 2007, p. 1624-1629.

Research output: Contribution to journalArticle

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