Heisenberg spin exchange (HE) studies of translational diffusion of the nitroxide radicals PD-tempone and P probe in two liquid crystalline solvents 60CB-80CB and 40,6 are described. It is shown that while PD-tempone undergoes strong exchange in the two solvents, the more anisotropic P-probe exhibits a tendency toward weak exchange which becomes more prominent in the low temperature mesophases. The molecular diffusion rates measured from our HE studies are compared with rates measured over larger distances using electron-spin resonance (ESR) imaging methods; we find that, in similar thermotropic liquid crystals, the former are somewhat faster. Also, while diffusion rates for PD-tempone (using HE) in the ordered phases of 60CB-80CB are consistent with a single activation energy, those in 40,6 show variations; suggesting that probe expulsion from core to chain regions in the former most likely occurs prior to SA formation, whereas in the latter it occurs in the SA phase. The absence of discontinuities in our diffusion data at the N-S A -RN transitions supports the belief that these transitions are subtle, with nothing dramatic occurring as the reentrant nematic (RN) phase is formed. The effect of including a potential of mean force U(r) between colliding radicals due to the liquid-crystal structure, is also considered. Our analyses indicate that the potential is of a repulsive nature [i.e., U( d) > 0] suggesting the possibility of solvent molecules inhibiting collisions of radicals at distances shorter than the sum of their solvated radii. The influence of orientational ordering on HE involving nonspherical radicals is considered, but changes from strong to weak exchange in the ordered phases appear to depend on how 'T the lifetime of the interacting radical pair is influenced by U(r). A careful effort is made to 1 separate the HE effects from the intermolecular electron-electron dipolar (EED) interactions. It is suggested that anomalies in D obtained from HE vs EED in this and earlier studies may also be rationalized in terms of the effects of U(r).

The phase behavior of 1,1′-di-O-eicosamethylene-2,2′-di-O-decylbis(glycero-3-phosphocholine) (1) and 1,1′-di-O-hexadecamethylene-2,2′-di-O-octylbis(glycero-3-phosphocholine) (2) was studied at the air-water interface and in aqueous dispersions using monolayer film balance, small-angle X-ray scattering, Raman spectroscopy, and cryo-TEM techniques. The limiting molecular areas (20 °C, pH 6.8) were observed to be 172 Å 2 for 2 and 105 Å 2 for 1, indicating a U-shaped configuration of the long polymethylene chains at the air-water interface. The larger molecular area of 2 relative to 1 at the air-water interface suggests that the alkyl chains of 2 are less ordered than those of 1 at similar pressures. The extrapolated d spacings for 1 from SAXS experiments were 32 Å in the liquid crystalline lamellar phase and 40 Å in the gel phase where the hydrocarbon chains are in their all trans configuration. The extrapolated d spacings for 2 were 27 and 33 Å in the liquid crystalline and gel phases, respectively. DSC analysis revealed phase transition temperatures of 1 and 2 in excess water at 15.3 and -23.5 °C, respectively, with observed transition enthalpies of 9.1 and 2.9 kJ/mol, respectively. These values are in good agreement with Raman spectroscopy experiments that detect alkyl melting transitions near these temperatures. Addition of 30 mol % cholesterol to both bolaamphiphile samples lowered the observed transition temperatures (1, 9.5 °C; 2, -25.1 °C) and enthalpies (1, 5.7 kJ/mol; 2, 2.5 kJ/mol), suggesting that cholesterol reduces the transition cooperativity. Extruded samples of pure 1 in buffer (30 mg/mL in 20 mM Tris, pH 8) produced vesicle structures that were variable in size (0.15-1.5 µm), with multilamellar and nonspherical morphologies apparent. Incorporation of cholesterol in the extruded samples (7:3 1/Chol), however, gave stable spherical unilamellar vesicles with a mean diameter of 857 ( 237 Å. Similar results were observed for dispersions of 2 and 7:3 2/Chol. These results suggest that stable, unilamellar monolayer membrane vesicles can be formed from bolaamphiphiles with relatively short (C16 and C20) membrane-spanning alkyl chains.

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The hydrophobic surfactant proteins SP-B and SP-C promote rapid adsorption of pulmonary surfactant to an air/water interface. Previous evidence suggests that they achieve this effect by facilitating the formation of a rate-limiting negatively curved stalk between the vesicular bilayer and the interface. To determine whether the proteins can alter the curvature of lipid leaflets, we used x-ray diffraction to investigate how the physiological mixture of these proteins affects structures formed by 1-palmitoyl-2-oleoyl phosphatidylethanolamine, which by itself undergoes the lamellar-to-inverse hexagonal phase transition at 71 degrees C. In amounts as low as 0.03% (w:w) and at temperatures as low as 57 degrees C, the proteins induce formation of bicontinuous inverse cubic phases. The proteins produce a dose-related shift of diffracted intensity to the cubic phases, with minimal evidence of other structures above 0.1% and 62 degrees C, but no change in the lattice-constants of the lamellar or cubic phases. The induction of the bicontinuous cubic phases, in which the individual lipid leaflets have the same saddle-shaped curvature as the hypothetical stalk-intermediate, supports the proposed model of how the surfactant proteins promote adsorption.

A carbon-doped silicon oxide (CDO) finds use as a material with a low dielectric constant (k) for copper interconnects in multilayered integrated circuits (ICs).

No abstract

Prior studies suggest that the hydrophobic surfactant proteins, SP-B and SP-C, promote adsorption of the lipids in pulmonary surfactant to an air-water interface by stabilizing a negatively curved rate-limiting structure that is intermediate between bilayer vesicles and the surface film. This model predicts that other peptides capable of stabilizing negative curvature should also promote lipid adsorption. Previous reports have shown that under appropriate conditions, gramicidin-A (GrA) induces dioleoyl phosphatidylcholine (DOPC), but not dimyristoyl phosphatidylcholine (DMPC), to form the negatively curved hexagonal-II (H(II)) phase. The studies reported here determined if GrA would produce the same effects on adsorption of DMPC and DOPC that the hydrophobic surfactant proteins have on the surfactant lipids. Small angle X-ray scattering and (31)P-nuclear magnetic resonance confirmed that at the particular conditions used to study adsorption, GrA induced DOPC to form the H(II) phase, but DMPC remained lamellar. Measurements of surface tension showed that GrA in vesicles produced a general increase in the rate of adsorption for both phospholipids. When restricted to the interface, however, in preexisting films, GrA with DOPC, but not with DMPC, replicated the ability of the surfactant proteins to promote adsorption of vesicles containing only the lipids. The correlation between the structural and functional effects of GrA with the two phospholipids, and the similar effects on adsorption of GrA with DOPC and the hydrophobic surfactant proteins with the surfactant lipids fit with the model in which SP-B and SP-C facilitate adsorption by stabilizing a rate-limiting intermediate with negative curvature.

To determine how the hydrophobic surfactant proteins promote insertion of the surfactant lipids into an air/water interface, we measured the effect of lysophosphatidylcholine (LPC) on adsorption. Existing models contend that the proteins function either by disordering the lipids or by stabilizing a negatively curved structure located between the adsorbing vesicle and the interface. Because LPC produces greater disorder but positive curvature, the models predict opposite effects. With vesicles containing either dioleoyl phosphatidylcholine (DOPC) or the neutral and phospholipids isolated from calf surfactant, LPC increased the initial rate at which surface tension fell. The final surface tension, however, remained well above the value of approximately 25 mN/m expected for a saturated surface. With two preparations, dioleoyl phosphatidylethanolamine and gramicidin A-DOPC, which form the negatively curved hexagonal-II (H(II)) phase and adsorb rapidly, LPC instead had little effect on initial adsorption but delayed the fall of surface tension below approximately 30 mN/m. LPC produced a similar inhibition of the late adsorption for extracted calf surfactant. Unlike dioleoyl phosphatidylethanolamine and gramicidin A-DOPC, small-angle x-ray scattering and (31)P-nuclear magnetic resonance for extracted calf surfactant detected no evidence for the H(II) phase. Our results indicate that although LPC can promote the initial adsorption of vesicles containing only lamellar lipids, it inhibits the facilitation by the hydrophobic proteins of late adsorption. Our findings support a model in which the surfactant proteins accelerate adsorption by producing a focal tendency to stabilize a negatively curved kinetic intermediate without a general shift to the H(II) phase.