A facile synthesis of fluorinated alkoxytrimethylsilanes using 1-methylimidazole as an acid scavenger
- Authors
- Lee, Bora; Kim, Jin Hyung; Lee, Hyunjoo; Ahn, Byoung Sung; Cheong, Minserk; Kim, Hoon Sik; Kim, Honggon
- Issue Date
- 2007-02
- Publisher
- ELSEVIER SCIENCE SA
- Citation
- JOURNAL OF FLUORINE CHEMISTRY, v.128, no.2, pp.110 - 113
- Abstract
- Fluorinated alkoxytrimethylsilanes (R1CH2OSiMe3), potential candidates for the third-generation cleaning agents, were synthesized in high yields over 95% from the reaction of chlorotrimethylsilane and fluorinated alcohol (R1CH2OH) in the presence of 1-methylimidazole. Elemental and H-1 NMR spectroscopic analysis showed that the reaction proceeds through the formation of an intermediate, 3-methyl-1-trimethylsilylimidazolium chloride. (c) 2006 Elsevier B.V. All rights reserved.
- Keywords
- CFC; SILICON; CFC; SILICON; chlorofluorohydocarbons; fluorinated alkoxytrimethylsilanes; CFC alternatives; 1-methylimidazolium chloride; ionic liquids
- ISSN
- 0022-1139
- URI
- https://pubs.kist.re.kr/handle/201004/134704
- DOI
- 10.1016/j.jfluchem.2006.10.008
- Appears in Collections:
- KIST Article > 2007
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.