Molecular dynamics study of low molecular weight gel forming salt-triggered dipeptide.

Molecular dynamics simulation method was used to study the aggregation of Na and Ca salts in different concentrations of Naphthalene-dipeptide (2NapFF) solutions. The results show that high-valence Ca2+ triggers the formation of a gel at a certain dipeptide concentration, and the low-valence Na+ system follows the aggregation law of general surfactants. The results also show that hydrophobic and electrostatic forces are the main driving forces for the formation of dipeptide aggregates, and that hydrogen bonds do not play a major role in the formation of dipeptide solution aggregates. Hydrophobic and electrostatic effects are the main driving forces for the formation of gels in dipeptide solutions triggered by Ca2+. Electrostatic attraction drives Ca2+ to form a weak coordination with four oxygen atoms on two carboxyl groups, which causes the dipeptide molecules to form a gel with a branched network structure.

A novel colorimetric and fluorescent probe based on a core-extended perylene tetra-(alkoxycarbonyl) derivative for the selective sensing of fluoride ions.

A novel fluoride (F-) colorimetric and fluorescent probe (P1) based on a core-extended perylene tetra-(alkoxycarbonyl) (PTAC) derivative was developed. The probe exhibited high sensitivity and selectivity for distinguishing F- from other common anions through significant changes of the UV-Vis and fluorescence spectra. Job's plot analysis revealed that the stoichiometry of the P1-F- interaction is 1 : 1. The association constant between P1 and F- was estimated to be 9.7 × 102 M-1 and the detection limit of F- was about 0.97 µM. An approximately 76 nm red-shift in the absorption and fluorescent quenching response was observed when F- was associated with P1. The emission intensity (I 574) decreased linearly along with the F- concentration from 3 × 10-5 M to 2 × 10-4 M. The mechanism of intermolecular proton transfer (IPT) was deduced based on the changes in the absorption, fluorescence, electrochemistry, and 1H NMR titration spectra. The density functional theory (DFT) theoretical results of the P1-F- complex are in good agreement with the experimental results. The rapid detection of F- ions in the solid state and living cells was also studied.

Vesicles of a new salt-free cat-anionic fluoro/hydrocarbon surfactant system.

Weakly basic tetradecyldimethylaminoxide (C14DMAO) molecules can be protonated to form a cationic surfactant, C14DMAOH+, by an acidic fluorocarbon surfactant, an 8-2-fluorotelomer unsaturated acid (C7F15CF==CHCOOH), to form a salt-free cationic and anionic (cat-anionic) fluoro/hydrocarbon surfactant system in aqueous solution. The high Krafft point of C7F15CF==CHCOOH was largely reduced as a result of being mixed with a C14DMAO micelle solution. A study of the phase behavior of the new salt-free cat-anionic fluoro/hydrocarbon surfactant system clearly indicates the existence of a birefringent Lalpha-phase region at (25.0+/-0.1) degrees C. The birefringent Lalpha phase consists of vesicles, which include uni- and multilamellar vesicles with one to dozens of shells, and oligovesicular vesicles, as demonstrated by freeze-fracture and cryo-transmission electron microscopy (FF- and cryo-TEM) images. The size distribution and structural transitions in the salt-free cat-anionic fluoro/hydrocarbon surfactant system were studied by dynamic light scattering (DLS) and 1H and 19F NMR spectroscopy. The formation of a salt-free cat-anionic vesicle phase could be induced by the strong electrostatic interaction between the cationic hydrocarbon C14DMAOH+ and the anionic fluorocarbon C7F15CF==CHCOO-, which provided evidence that the electrostatic interaction between the cationic and anionic surfactants is larger than the nonsynergistic interaction between the stiff fluorocarbon and the soft hydrocarbon chains of the surfactants.

Ca2+- and ba2+-ligand coordinated unilamellar, multilamellar, and oligovesicular vesicles.

Ca(2+)- and Ba(2+)-coordinated vesicle phases were prepared in mixed aqueous solutions of tetradecyldimethylamine oxide (C(14)DMAO) and calcium oleate (Ca(OA)(2)) or barium oleate (Ba(OA)(2)). At the right mixing ratios, metal-ligand coordination between Ca(OA)(2) or Ba(OA)(2) and C(14)DMAO results in the formation of molecular bilayers due to the reduction in area per head group. Ca(2+) and Ba(2+) tightly associate to the head groups of surfactants and in this system the bilayer membranes are not shielded by excess salts. The structures of the birefringent samples of the Ca(OA)(2)/C(14)DMAO/H(2)O and Ba(OA)(2)/C(14)DMAO/H(2)O systems were determined by freeze-fracture transmission electron microscopy (FF-TEM), small-angle X-ray scattering (SAXS), and rheological measurements to consist of unilamellar, multilamellar, and oligovesicular vesicles. The coordination between C(14)DMAO and Ba(OA)(2) or Ca(OA)(2) plays an important role in the formation of the vesicles, which was easily confirmed by studying the phase behavior of the KOA/C(14)DMAO/H(2)O system in which only the L(1) phase forms, due to the absence of coordination between KOA and C(14)DMAO. A mechanism is proposed that accounts for the formation of these new metal-ligand coordinated vesicles.

A salt-free zero-charged aqueous onion-phase enhances the solubility of fullerene C60 in water.

An onion-phase (multilamellar vesicular phase or Lalpha-phase) was prepared from salt-free zero-charged cationic and anionic (catanionic) surfactant mixtures of tetradecyltrimethylammonium hydroxide (TTAOH)/lauric acid (LA)/H2O. The H+ and OH- counterions form water (TTAOH + LA --> TTAL + H2O), leaving the solution salt free. The onion-phase solution has novel properties including low conductivity, low osmotic pressure and unscreened electrostatic repulsions between cationic and anionic surfactants because of the absence of salt. The spherical multilamellar vesicles have an average 250 nm radius as measured by freeze-fracture transmission electron microscopy (FF-TEM) and the maximum interlayer distance, i.e., the thickness of the hydrophobic bilayer and the water layer, was calculated to be around 52 nm by small-angle X-ray scattering (SAXS). Extremely hydrophobic C60 fullerene can be solubilized in this salt-free zero-charged aqueous onion-phase. As a typical result, 0.588 mg.mL(-1) (approximately 0.82 mmol.L(-1)) C60 has been successfully solubilized into a 50 mmol.L(-1) catanionic surfactant onion-phase aqueous solution. The weight ratio of fullerene to TTAL is calculated to be around 1:40. Solubilization of C60 in the salt-free catanionic onion-phase solution was investigated by using different sample preparation routes, and a variety of techniques were used to characterize these vesicular systems with or without encapsulated C60. The onion-phase solution changed color from slightly bluish to yellow or brown after C60 was solubilized. 1H and 13C NMR measurements indicated that the C60 molecules are located in the hydrophobic layers, i.e., in the central positions [omega-CH3 and delta-(CH2)x] of the hydrophobic layers of the TTAL onion-phase. Salt-free zero-charged catanionic vesicular aqueous solutions are good candidates for enhancing the solubility of C60 in aqueous solutions and may broaden the functionality of fullerenes to new potential applications in biology, medicine, and materials. Hopefully, our method can also be extended to solubilize functionalized carbon nanotubes in aqueous solutions.

Two routes to vesicle formation: metal-ligand complexation and ionic interactions.

Two routes to vesicle formation were designed to prepare uni- and multilamellar vesicles in salt-free aqueous solutions of surfactants. The formation of a surfactant complex between a double-chain anionic surfactant with a divalent-metal ion as the counterion and a single-chain zwitterionic surfactant with the polar group of amine-oxide group is described for the first time as a powerful driving force for vesicle-phases constructed from salt-free mixtures of aqueous surfactant solutions. As a typical example, a Zn(2+)-induced charged complex fluid, vesicle-phase has been studied in aqueous mixtures of tetradecyldimethylamine oxide (C(14)DMAO) and zinc 2,2-dihydroperfluorooctanoate [Zn(OOCCH(2)C(6)F(13))(2)]. This ionically charged vesicle-phase formed due to surfactant complexation has interesting rheological properties and is not shielded by excess salts because there are no counterions in the solution. Such a vesicle-phase of surfactant complex is important for many applications; for example, the vesicle-phase was further used to produce in situ the vesicle-phase of the salt-free cationic/anionic (catanionic) surfactants, C(14)DMAOH(+)-(-)OOCCH(2)C(6)F(13). The salt-free catanionic vesicle-phase could be produced through injecting H(2)S gas into the C(14)DMAO/Zn(OOCCH(2)C(6)F(13))(2) vesicle-phase, because the zwitterionic surfactant C(14)DMAO can be charged by the H(+) released from H(2)S to become a cationic surfactant and Zn(2+) was precipitated as ZnS. After the ZnS precipitates were removed from C(14)DMAO/Zn(OOCCH(2)C(6)F(13))(2) solutions, the final mixed solution does not contain excess salts as do other cationic/anionic surfactant systems. Both the C(14)DMAO-Zn(OOCCH(2)C(6)F(13))(2) complex and the resulting catanionic C(14)DMAOH(+)-(-)OOCCH(2)C(6)F(13) solution are birefringent Lalpha-phase solutions that consist of uni- and multilamellar vesicles. Ring-shaped semiconductor ZnS materials with encapsulated ZnS precipitates and regular spherical ZnS particles were prepared, which resulted in a transition from vesicles composed of metal-ligand complexes to vesicles held together by ionic interactions in the salt-free aqueous systems. This strategy should provide a new method to prepare inorganic materials. The present routes to form vesicles solve a problem: how to prepare nanomaterials using surfactant self-assembly, with structure controlled not by the growing material, but by the phase behavior of the surfactants.