Azaylide-based gemini amphiphiles displaying unique self-assembling behavior <i>via</i> an even-odd effect of alkyl linker chain length.
basic_science · Level V
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- Record sourced from PubMed, PMID 39108245.
- Also identified by DOI 10.1039/d4sm00789a.
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Abstract
Herein, we report a straightforward synthesis of azaylide-based gemini amphiphiles using bis(diphenylphosphino)alkanes <i>via</i> the Staudinger reaction. The prepared gemini amphiphiles exhibited an even-odd effect in their self-assembly behavior depending on the length of the alkyl linkers. Furthermore, the assembled micelles had high host capability toward hydrophobic guests in water.