Pressure effects on bending elasticities of surfactant monolayers in a ternary microemulsion composed of aerosol-OTD2O/decane

Pressure effects on the bending elasticities of surfactant monolayers have been investigated in a microemulsion system composed of aerosol-OT (AOT), D2O, and deuterated decane by means of small angle neutron scattering, neutron spin echo (NSE), and dynamic light scattering (DLS). In this system, a water-in-oil droplet structure, at ambient temperature and pressure, decomposes into two phases, under both increasing temperature and pressure. The authors' previous study showed that the bending modulus kappa of monolayers slightly decreased with increasing temperature, while it increased with increasing pressure. Temperature and pressure dependencies of kappa were explained in terms of a microscopic model, which takes into account the interactions between surfactant molecules. In this paper, the authors present the temperature and pressure dependencies of kappa obtained by the analysis combined with DLS and NSE experiments. The values of the bending modulus and mean displacement of the second-order droplet deformation are reasonable. It was further confirmed that an increase in the attractive interaction between hydrocarbon tails of AOT molecules with increasing pressure could be the origin of the pressure-induced phase transition.     

Contribution of stress wave and cavitation bubble in evaluation of cell–cell adhesion by femtosecond laser-induced impulse

When an intense femtosecond laser is focused in a cell culture medium, shock wave, stress wave, and cavitation bubble are generated at the laser focal point. Cell–cell adhesion can be broken at the cellular level by the impacts of these factors. We have applied this breaking of the adhesion to an estimation of the cell–cell adhesion strength. In this application, it is important to identify which of these factors is the dominant factor that breaks the adhesion. Here we investigated this issue using streptavidin-coated microbeads adhering to a biotin-coated substrate as a mimic of the cell–cell adhesion. The results indicated that the break was induced mainly by the stress wave, not by the impact of the cavitation bubble.     

Irreversible magnetovolume effect in Nd7Rh3 single crystal

Magnetovolume effect in Nd₇Rh₃ single crystal has been studied by measuring the magnetostriction as a function of external magnetic field at 4.2 K. An irreversible magnetovolume effect having a negative remanent volume magnetostriction was observed when the external magnetic field was applied along the b-axis. The irreversible magnetostrictive effect takes place in the longitudinal magnetostriction along the b-axis. The remanent magnetostriction along the b-axis relaxes after removing external magnetic field for several hours and equilibrium state is stabilized.     

A purification system for 64Cu produced by a biomedical cyclotron for antibody PET imaging

Ion exchange is a simple and efficient method for separating no-carrier-added ⁶⁴Cu from an irradiated Ni target. We developed a semi-automated two-round ⁶⁴Cu separation system equipped with a strong-base anion exchange resin column. We first verified the efficiency of the system using a non-radioactive substitute consisting of 25 mg of Ni and 127 ng of Cu, and confirmed that Cu was completely eluted at the second round of the separation step. After the bombardment, separation of ⁶⁴Cu from the Ni target was achieved with high radiochemical purity. ⁶⁴Cu produced and separated in this study had an extremely low level of Ni impurity. It could be used for labeling monoclonal antibodies for antibody positron emission tomography imaging and synthesizing radiopharmaceuticals.     

Unique inclusion behaviour of 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetraaminothiacalix[4]-arene towards small organic molecules

Tetraaminothiacalixarene 3, bearing four amino groups instead of the hydroxy groups of p-tert-butylthiacalix[4]arene 2, exhibits inclusion properties different from those of compound 2 towards small organic molecules upon crystallisation from neat solvents or guest solutions. X-ray crystallographic analyses reveal that nitromethane and acetonitrile are included into the cone-shaped cavity of compound 3, as is often seen in inclusion crystals of compound 2, whereas dichloromethane occupies a space between two distal benzene rings of compound 3, adopting a 1,3-alternate conformation. Acetic acid, which forms a dimer, fills a pore surrounded by four host molecules with a pinched cone conformation. Furthermore, guest-free crystals of compound 3 with a 1,3-alternate conformation absorb acetonitrile to give inclusion crystals with the same crystal structure as that obtained by the crystallisation. Thus, compound 3 flexibly changes its conformation according to the structures of guest compounds.     

Measurements on diproton emission from the break-up channels of 23Al and 22Mg

Two-proton relative momentum distributions from the break-up channels ²³Al→p+p+²¹Na and ²²Mg→p+p+²⁰Ne at an energy of 60–70 A MeV have been measured together with two-proton opening angles at the projectile fragment separator beamline (RIPS) in the RIKEN Ring Cyclotron Facility. The results demonstrate the existence of diproton emission component from single-step ²He for highly excited ²³Al and ²²Mg.     

Infrared studies of stereoregular polymerization of methyl methacrylate and methacrylonitrile by organometallic compounds

Infrared spectra of reaction mixtures of methyl methacrylate or methacrylonitrile with an equimolar amount of organometallic compounds were investigated in relation to the stereoregulating ability of the catalysts in polymerization. It was found that the carbonyl or nitrile stretching frequency correlated with the stereoregularity of polymers prepared with the corresponding catalysts; i.e., the higher the frequency, the higher the isotacticity. From these results a mechanism of isotactic polymer formation was proposed, in which catalyst counterion was located near the carbonyl group in polymer terminal and that of monomer to be reacted, and consequently the isotactic polymerization is facilitated.