Preparation of alkyl-substituted partial trimethylsilyl silicates from olivine

Kazuyuki Kuroda, Tetsuhiro Koike, Chuzo Kato*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)


The direct trimethylsilylation reaction of olivine has yielded partial trimethylsilyl derivatives of ortho- and di-silicates whose unsilylated silanol groups have been esterified with the alcohol used as the organic solvent in the trimethylsilylating reagent. Gas chromatographic-mass spectroscopic measurements indicate the presence of the tri-, di-, and mono-alkyl-substituted trimethylsilyl derivatives of monosilicic acid [SiO4(SiMe3)4-nRn; n = 1-3] in addition to the fully silylated monomeric derivative [SiO4(SiMe3)4]. Dimeric derivatives have also been detected which contain both the completely trimethylsilylated derivative [Si2O7(SiMe3)6] and alcohol-esterified derivatives [Si2O7(SiMe3)6-nRn; n = 1-4]. The ratio of the esterified products varies with the volume of alcohol or water in the silylating reagent as well as with the reaction time.

Original languageEnglish
Pages (from-to)1957-1960
Number of pages4
JournalJournal of the Chemical Society, Dalton Transactions
Issue number9
Publication statusPublished - 1981 Dec 1

ASJC Scopus subject areas

  • Chemistry(all)


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