Displacement Plating of a Mesoporous Pt Skin onto Co Nanochains in a Low‐Concentration Surfactant Solution

Mesoporous Pt skins on Co nanochains are successfully synthesized by a displacement reaction between Pt species and a Co support with the assistance of surfactant micelles. The assembly of surfactant micelles on Co nanochains plays a key role in the formation of mesoporous Pt layers. The evolution of the mesoporous Pt layers is carefully studied at different time intervals. As the reaction time increases, the mesoporous Pt layers become thicker, and well‐defined mesoporous structures gradually develop. The obtained mesoporous Pt skin exhibits high activity and superior CO tolerance in the electro‐oxidation reaction of methanol. The mesoporous Pt skin also shows very high durability, and only a 20.2 % loss of the Pt electrochemical surface area is found even after a harsh durability test.     

Characteristic near-field spectra of single gold nanoparticles

We report on results for the in silico screening of a database of 10 000 flexible compounds against various crystal structures of the thymidine kinase enzyme complexed with 10 known inhibitors. We provide a quantitative analysis of the deviations in the ranking of the inhibitors depending on the choice of receptor conformation and imply that the inclusion of side-chain degrees of freedom to the receptor would significantly improve the predictive power of the screening approach. We suggest a consensus score that, in the case of several known native structures of the receptor, enables the evaluation of scoring functions without the requirement of explicit receptor-flexibility.     

Novel thermo-responsive coloring phenomena in water/surfactant/oil emulsions

Emulsions comprising a dual-surfactant system of a long-chain amidoamine derivative and a quaternary ammonium salt developed an iridescent color at a specific temperature region. The emulsions underwent phase inversion on heating from an O/W emulsion to a W/O emulsion, passing through a periodical lamellar structure which developed a characteristic interference color. Interestingly, the color and the coloring temperature can be independently controlled by adjusting the concentration of surfactants, respectively.     

Wittig reaction with ion-supported Ph3P

Ion-supported Ph₃P, 4-(diphenylphosphino)benzyltrimethylammonium bromide A and N-methyl-N-[4-(diphenylphosphino)benzyl]pyrrolidinium bromide B, were used for the Wittig reaction. Ion-supported phosphonium salts A1 and B1, which were prepared from the reactions of ion-supported Ph₃P A and B with ethyl bromoacetate, respectively, reacted with aromatic and aliphatic aldehydes in the presence of K₂CO₃ to give the corresponding α,β-unsaturated ethyl esters in good yields with high purity by simple filtration of the reaction mixture and subsequent removal of the solvent from the filtrate. Similarly, ion-supported phosphonium salts A2 and B2, which were prepared from the reactions of ion-supported Ph₃P A and B with p-methylbenzyl bromide, respectively, reacted with aromatic and aliphatic aldehydes in the presence of NaH to provide the corresponding p-methylstyrene derivatives in good yields with high purity by simple filtration of the reaction mixture and the subsequent removal of the solvent from the filtrate. In both reactions, the co-product, ion-supported Ph₃PO, could be obtained quantitatively by simple filtration, and was converted into the corresponding ion-supported Ph₃P A and B again in high yields using dimethyl sulfate, followed by the reduction with LiAlH₄. Recovered and regenerated ion-supported Ph₃P A and B could be reused for the same Wittig reaction while maintaining good yields of ethyl (E)-3-(4′-chlorophenyl)-2-propenoate and 1-(4′-chlorophenyl)-2-(4″-methylphenyl)ethene with high purity by simple filtration and removal of the solvent from the filtrate.     

Near-field optical imaging of enhanced electric fields and plasmon waves in metal nanostructures

In this article, studies on noble metal nanostructures using near-field optical microscopic imaging are reviewed. We show that near-field transmission imaging and near-field two-photon excitation imaging provide valuable methods for investigation of plasmon resonances in metal nanostructures. The eigenfunctions of plasmon modes in metal nanoparticles are directly visualized using these methods. For metal nanowire systems, wavevectors of the longitudinal plasmon modes can be estimated directly from the wave-function images, and the dispersion relations are plotted and analyzed. Using ultrafast transient near-field imaging, we show that the deformation of the plasmon wave function takes place after photoexcitation of a gold nanorod. Such methods of plasmon-wave imaging may provide a unique basic tool for designing plasmon-mode-based nano-optical devices. We also demonstrate that the near-field two-photon excitation probability images reflect localized electric-field enhancements in metal nanostructures. We apply this method to gold nanosphere assemblies and clearly visualize the local enhanced optical fields in the interstitial sites between particles (hot spots). We also show the contribution of hot spots to surface enhanced Raman scattering. The methodology described here may provide valuable basic information about the characteristic enhanced optical fields in metal nanostructures as well as on their applications to new innovative research areas beyond the conventional scope of materials.     

Naturally engineered glycolipid biosurfactants leading to distinctive self-assembled structures

Self-assembling properties of "natural" glycolipid biosurfactants, mannosyl-erythritol lipids A and B (MEL-A, MEL-B), which are abundantly produced from yeast strains, were investigated by using the fluorescence-probe method, dynamic light-scattering (DLS) analysis, freeze-fracture transmission electron microscopy (FF-TEM), and synchrotron small/wide-angle X-ray scattering (SAXS/WAXS) analysis, among other methods. Both MEL-A and MEL-B exhibit excellent self-assembly properties at extremely low concentrations; they self-assemble into large unilamellar vesicles (LUV) just above their critical-aggregation concentration (CAC). The CAC(I) value was found to be 4.0x10(-6) M for MEL-A and 6.0x10(-6) M for MEL-B. Moreover, the self-assembled structure of MEL-A above a CAC(II) value of 2.0x10(-5) M was found to drastically change into sponge structures (L3) composed of a network of randomly connected bilayers that are usually obtained from a complicated multicomponent "synthetic" surfactant system. Interestingly, the average water-channel diameter of the sponge structure was 100 nm. This is relatively large compared with those obtained from "synthetic" surfactant systems. In addition, MEL-B, which has a hydroxyl group at the C-4' position on mannose instead of an acetyl group, gives only one CAC; the self-assembled structure of MEL-B seems to gradually move from LUV to multilamellar vesicles (MLV) with lattice constants of 4.4 nm, depending on the concentration. Furthermore, the lyotropic-liquid-crystal-phase observation at high concentrations demonstrates the formation of an inverted hexagonal phase (H2) for MEL-A, together with a lamella phase (L(alpha)) for MEL-B, indicating a difference between MEL-A and MEL-B molecules in the spontaneous curvature of the assemblies. These results clearly show that the difference in spontaneous curvature caused by the single acetyl group on the head group probably decides the direction of self-assembly of glycolipid biosurfactants. The unique and complex molecular structures with several chiral centers that are molecularly engineered by microorganisms must have led to the sophisticated self-assembling properties of the glycolipid biosurfactants.     

Modification of nitroxyl contrast agents with multiple spins and their proton T(1) relaxivity

The purpose of this study is to test the performance of multispin nitroxyl contrast agents in improving the sensitivity of MR detection for nitroxyl contrast agents. The relation between T(1) relaxivity and the number of paramagnetic centers in a molecule was investigated. Compound 1 is a single molecule of methoxycarbonyl-PROXYL (MC-PROXYL). Two and three MC-PROXYL molecules were chemically coupled to obtain Compounds 2 and 3, which have two and three nitroxyl spins in the molecule, respectively. A good linear relation, the slope of which increased depending on the number of nitroxyl spins in the molecule, was obtained between T(1)-weighted (fast low-angle shot) MR image contrast enhancement at 7 T and the concentration of nitroxyl contrast agents. T(1)-weighted MR image contrast enhancement and T(1) relaxivity levels of nitroxyl contrast agents were increased depending on the number of nitroxyl spins in the molecule. Multicoupling nitroxyl molecules can enhance the T(1)-weighted contrast effect while maintaining the quantitative behavior of the molecule for up to three spins.     

Cerebral infarction associated with moyamoya disease: histogram-based quantitative analysis of diffusion tensor imaging -- a preliminary study

Moyamoya disease (MMD) is a rare disorder of unknown etiology in which terminal portions of the internal carotid arteries become steno-occlusive, with fine collateral "moyamoya vessels" formed secondarily, resulting in serial ischemic strokes throughout its clinical course. Whole-brain histogram (WBH) of diffusion tensor imaging (WBH-DTI) is an analytical tool whose feasibility has been ascertained in various pathologies. To elucidate whether WBH-DTI could detect any difference between ischemic MMD and normal controls, we examined 27 consecutive MMD patients without hemorrhage and 48 normal controls in this prospective study using a 3.0-T magnetic resonance scanner. WBHs of fractional anisotropy (FA) (WBH-FA) and mean diffusivity (MD) (WBH-MD) were compared among three groups: Group 1, MMD patients with infarct (n=15); Group 2, MMD patients without infarct (n=12); and Group 3, normal controls (n=48). Group 1 showed significantly higher peak height and significantly lower mean value on WBH-FA, as well as significantly lower peak height and significantly higher mean value on WBH-MD, compared with Groups 2 and 3. No significant difference was seen in parameters at either WBH-FA or WBH-MD between Groups 2 and 3. These results might reflect the pathological severity of each group, and WBH-DTI could feasibly detect differences between ischemic MMD with infarction and MMD without infarction and normal controls.     

Contrast changes in portal vein and bile duct between centric and linear k-space ordering on three-dimensional segmented true fast imaging with steady-state precession magnetic resonance imaging

Purpose

To compare the degree of visualization of the bile duct and portal vein in terms of the difference in k-space ordering on a three-dimensional (3D) segmented true fast imaging with steady-state precession (trueFISP) sequence.

Materials and Methods

A breath-hold coronal 3D segmented trueFISP sequence was prospectively performed on 14 healthy volunteers. Images obtained with centric and linear k-space ordering in the k(x)–k(y) plane were compared by two independent radiologists qualitatively with depiction scores on a five-point scale (1=not seen to 5=excellent depiction) using the Wilcoxon signed-rank test. Images were also compared quantitatively using relative contrast values for the bile duct and portal vein against the hepatic parenchyma using a paired t-test.

Results

With centric ordering, both the mean depiction scores and relative contrast values for the portal vein were significantly lower than those with linear ordering (1.5 vs. 3.5, P<.01; and 0.08±0.19 vs. 0.51±0.10, P<.01, respectively). However, in the bile duct, there were no significant differences, only slight differences were found among the results obtained with centric and linear ordering (3.9 vs. 3.8, P=.72; and 0.59±0.06 vs. 0.68±0.06, P<.01, respectively).

Conclusion

For visualizing the bile duct, centric k-space ordering on 3D segmented trueFISP sequence is recommended, while linear ordering is recommended for portal vein visualization.