4.5 Article

Symmetric and Asymmetric Bolaamphiphiles from Ascorbic Acid

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 115, Issue 40, Pages 11638-11649

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp204920y

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Funding

  1. Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase (CSGI, Florence)
  2. Ministero dell'Istruzione, dell'Universita e della Ricerca (MIUR, Rome)
  3. CNR

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The properties of novel bolaamphiphiles that carry epimers of vitamin C (L-ascorbic acid and/or D-isoascorbic acid) as hydrophilic head groups, and an interconnecting aliphatic C-12 chain (DD, DL, and LL) were investigated by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), small-angle X-ray scattering (SAXS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) in the solid state (anhydrous powders) and in aqueous dispersions as a function of the surfactant concentration. Upon heating, the aqueous dispersions undergo a phase transition from a hydrated semicrystalline coagel to a micellar phase. The results suggest that the headgroup chirality determines the formation of either inter- or intramolecular hydrogen bonds between the polar heads, which affect the phase behavior and structural properties of the nanoassemblies produced by these surfactants in water dispersions. The DSC data of aqueous dispersions were analyzed to obtain the size distribution of the pores in the coagel state.

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