Real space observation of current-induced magnetic domain wall displacement in Co/Ni nano-wire by photoemission electron microscopy

Current-induced magnetic domain wall (DW) displacement in a Co/Ni nano-wire with perpendicular magnetic anisotropy was investigated in real space by photoemission electron microscopy (PEEM) for the first time. DW velocity determined from the PEEM observation was 40?m?s(-1) for the current density of 2.5?×?10(12)?A?m(-2), which was consistent with the result obtained by the electrical measurement used in our previous reports.     

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.     

Formation of a Thymine‐HgII‐Thymine Metal‐Mediated DNA Base Pair: Proposal and Theoretical Calculation of the Reaction Pathway

A reaction mechanism that describes the substitution of two imino protons in a thymine:thymine (T:T) mismatched DNA base pair with a Hg^II ion, which results in the formation of a (T)N3‐Hg^II‐N3(T) metal‐mediated base pair was proposed and calculated. The mechanism assumes two key steps: The formation of the first Hg^II? N3(T) bond is triggered by deprotonation of the imino N3 atom in thymine with a hydroxo ligand on the Hg^II ion. The formation of the second Hg^II? N3(T) bond proceeds through water‐assisted tautomerization of the remaining, metal‐nonbonded thymine base or through thymine deprotonation with a hydroxo ligand of the Hg^II ion already coordinated to the thymine base. The thermodynamic parameters ΔG_R=?9.5 kcal mol^?1, ΔH_R=?4.7 kcal mol^?1, and ΔS_R=16.0 cal mol^?1 K^?1 calculated with the ONIOM (B3LYP:BP86) method for the reaction agreed well with the isothermal titration calorimetric (ITC) measurements by Torigoe et al. [H. Torigoe, A. Ono, T. Kozasa, Chem. Eur. J. 2010 , 16, 13218–13225]. The peculiar positive reaction entropy measured previously was due to both dehydration of the metal and the change in chemical bonding. The mercury reactant in the theoretical model contained one hydroxo ligand in accord with the experimental pK_a value of 3.6 known for an aqua ligand of a Hg^II center. The chemical modification of T:T mismatched to the T‐Hg^II‐T metal‐mediated base pair was modeled for the middle base pair within a trinucleotide B‐DNA duplex, which ensured complete dehydration of the Hg^II ion during the reaction.     

Detection of single nucleotide polymorphisms by the specific interaction between transition metal ions and mismatched base pairs in duplex DNA

Single nucleotide polymorphisms (SNPs) are base differences in the human genome. These differences are favorable markers for genetic factors including those associated with risks of complex diseases and individual responses to drugs. When two duplex DNAs with different types of SNPs are mixed and reannealed, the two novel heteroduplexes containing mismatched base pairs are formed in addition to the two initial perfectly matched homoduplexes. Heteroduplex analysis recognizing the newly formed mismatched base pairs is useful for SNP detection. Various strategies to detect the mismatched base pairs were devised due to the potential applications of SNPs. However, they were not always convenient and accurate. Here, we propose a novel strategy to detect the mismatched base pairs by the specific interaction between the Hg²⁺ ion and a T:T mismatched base pair and that between the Ag⁺ ion and a C:C mismatched base pair. UV melting indicated that the melting temperature of only the heteroduplexes with the T:T and C:C mismatched base pair specifically increased on adding the Hg²⁺ and Ag⁺ ion, respectively. Fluorescence resonance energy transfer analyses indicated that the intensity of fluorophore emission of only the fluorophore and quencher-labeled heteroduplexes with the T:T and C:C mismatched base pair specifically decreased on adding the Hg²⁺ and Ag⁺ ion, respectively. We propose that the addition of the metal ion could be a convenient and accurate strategy to detect the mismatched base pair in the heteroduplex. This novel strategy might make the heteroduplex analysis easy and eventually lead to better SNP detection.     

Application of 85Kr dating to groundwater in volcanic aquifer of Kumamoto Area, Japan

Groundwater age was determined by ⁸⁵Kr/Kr specific activity of gases dissolved in groundwater at Kumamoto Area, in which newly developed Kr extraction system and liquid scintillation counting technique for ⁸⁵Kr were applied. Apparent mean residence times observed were 8.2 ± 0.7 years and 20.7 ± 0.6 years for the groundwater taken from a well at the recharge area and that from an artesian borehole at the discharge area, respectively showing a consistent age trend estimated from the observed groundwater flow system of Kumamoto Area and also that determined using environmental tritium. Similar mean residence times of ⁸⁵Kr and tritium were observed at the discharge area but the mean residence time of ⁸⁵Kr at the recharge area was younger compared to that of tritium, probably due to mixing of river water containing recent ⁸⁵Kr high in concentration into groundwater flow coming from the northern upland??s recharge area. The mean residence time of the groundwater flow coming from northern upland area and a traveling time of the groundwater between two sampling points were estimated by a simple model assuming mixing the river water with the groundwater and a piston flow between two sampling points.     

Uniqueness and Examples of Compact Toric Sasaki-Einstein Metrics

In [11] it was proved that, given a compact toric Sasaki manifold with positive basic first Chern class and trivial first Chern class of the contact bundle, one can find a deformed Sasaki structure on which a Sasaki-Einstein metric exists. In the present paper we first prove the uniqueness of such Einstein metrics on compact toric Sasaki manifolds modulo the action of the identity component of the automorphism group for the transverse holomorphic structure, and secondly remark that the result of [11] implies the existence of compatible Einstein metrics on all compact Sasaki manifolds obtained from the toric diagrams with any height, or equivalently on all compact toric Sasaki manifolds whose cones have flat canonical bundle. We further show that there exists an infinite family of inequivalent toric Sasaki-Einstein metrics on for each positive integer k.     

Application of spectroscopic photoemission and low energy electron microscope to high-k gate dielectrics: Relationship between surface morphology and electronic states during Hf-silicide formation

We have applied the spectroscopic photoemission and low energy electron microscope to study high-k gate dielectrics and have performed the following in situ operations during ultrahigh vacuum annealing: real-time observation of surface morphology and microregion photoelectron spectroscopy measurements. Changes in surface morphology and electronic states were consistent with the models previously reported in the case of HfO₂/Si. No clear differences between void regions and nonvoid regions have been observed in microregion photoelectron spectra for poly-Si/HfO₂/Si, regardless of phase separation in real space. These results have suggested that the initial void formation occurs in about 100-nm wide regions for both HfO₂/Si and poly-Si/HfO₂/Si.     

On Global Existence,Asymptotic Stability and Blowing Up of Solutions for Some Degenerate Non-linear Wave Equations of Kirchhoff Type with a Strong Dissipation

We study on the initial-boundary value problem for some degenerate non-linear wave equations of Kirchhoff type with a strong dissipation: When the initial energy $E(u_0,u_1)\equiv \left\| u_1\right\| ⁁2+\frac 1{\gamma +1}\left\| \nabla u_0\right\| ⁁{2(\gamma +1)}-\frac 2{\alpha +2}\left\| u_0\right\| _{\alpha +2}⁁{\alpha +2}$ associated with the equations is non-negative and small, a unique (weak) solution exists globally in time and has some decay properties. When the initial energy E(u₀,u₁) is negative, the solution blows up at some finite time. In the proof we use the ‘modified potential well’ and ‘Concavity’ methods. © 1997 by B.G. Teubner Stuttgart-John Wiley & Sons, Ltd.     

Novel synthesis of polymeric phase transfer catalysts containing N,N-dialkylacrylamide unit and their catalytic activity

Soluble polymeric phase transfer catalysts (PTCs) containing benzyltributylphosphonium chloride moieties and polar N,N-dialkyl-acrylamide with long alkyl groups such as N,N-dipropylacrylamide, N,N-dibutylacrylamide, N,N-dihexylacrylamide, and N,N-dioctylacrylamide were prepared via two-step reactions from p-chloromethylstyrene and the corresponding N,N-dialkylacrylamide. When the obtained polymers were added, the phase transfer catalyzed reaction of benzylchloride with solid potassium acetate to proceed smoothly. The catalytic activity was strongly affected by the content of phosphonium chloride and the varieties of comonomer unit in the polymeric PTC. The polymeric PTC containing the N,N-dihexylacrylamide unit showed excellent high catalytic activity in a low polar solvent such as the mixed solvent of toluene with 70 vol % n-tridecane. Therefore, the polymer containing lipophilic long chains such as the hexyl group is desirable for polymeric PTC. © 1996 John Wiley & Sons, Inc.