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PH-dependent chiral vesicles from enantiomeric sodium 2,3-bis(decyloxy) succinate in aqueous solution
Balachandran Vijai Shankar,
Published in
2007
PMID: 17335249
Volume: 23
   
Issue: 7
Pages: 3523 - 3529
Abstract
Enantiomeric, twin-tailed, twin-chiral, sodium (2R,3R)-(+)-bis(decyloxy) succinate and sodium (2S,3S)-( - )-bis-(decyloxy)succinate have been synthesized and characterized. Surface tension, conductivity, and steady-state fluorescence spectroscopic measurements confirmed the presence of two aggregation concentrations, namely, the critical micellar concentration (CMC) and the critical vesicle concentration (CVC). The compounds behaved as true surfactants, with a CMC of 0.05 mM, and formed vesicles spontaneously in aqueous solution at a CVC of 0.14 mM. The compounds formed myelin figures in contact experiments, suggesting the formation of bilayers in aqueous solution culminating into individual vesicles. The vesicles were of 500-800 nm size and formed egg shells, porous spheres, and multivesicular vesicles, confirmed from transmission electron microscopy and optical microscopic techniques. The vesicles were found to be pH sensitive, were stable in the pH range 6-8, and formed the insoluble diacid at acidic pH due to protonation of the carboxylate head groups. © 2007 American Chemical Society.
About the journal
JournalLangmuir
ISSN07437463
Open AccessNo
Concepts (27)
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    Bubbles (in fluids)
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    Chirality
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    Critical micelle concentration
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    Electric conductivity
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    Fluorescence spectroscopy
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    Ph effects
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    Solutions
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    Surface tension
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    Carboxylates
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    FLUORESCENCE SPECTROSCOPIC MEASUREMENT
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    MULTIVESICULAR VESICLES
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    Vesicles
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    Sodium compounds
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    SUCCINIC ACID DERIVATIVE
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    Surfactant
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    Article
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    Chemistry
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    Micelle
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    pH
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    Stereoisomerism
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    Synthesis
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    Transmission electron microscopy
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    Hydrogen-ion concentration
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    Micelles
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    Microscopy, electron, transmission
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    Succinates
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    Surface-active agents