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- W2078204806 abstract "New amphiphilic cyclodextrins are synthesized by selective modification. Two synthetic strategies are investigated. Per-(6-thio-2,3-trimethylsilyl)cyclodextrins can only be obtain by synthesizing first the per-6-thio-cyclodextrin and then silylating the remaining hydroxy functions. Characterizations of the products were achieved by ESI-MS and intramolecular coupling between thiol functions was evidenced. These new compounds are shown to be amphiphilic, and form stable Langmuir–Blodgett films that can be transferred on the upstroke and the downstroke of a substrate with a transfer ratio close to unity." @default.
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- W2078204806 date "2008-08-01" @default.
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- W2078204806 title "Synthesis and characterization of amphiphilic per-(6-thio-2,3-trimethylsilyl)cyclodextrin: Application to Langmuir film formation" @default.
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- W2078204806 doi "https://doi.org/10.1016/j.carbpol.2007.12.031" @default.
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