Isovector quadrupole resonance observed in the 60Ni(13C,13N)60Co reaction at E/A=100 MeV

The charge-exchange reaction 60Ni(13C,13N)60Co at E/A=100 MeV has been studied to locate isovector (deltaT=1) non-spin-flip (deltaS=0) giant resonances. Besides the giant dipole resonance at E(x)=8.7 MeV, another resonance has been observed at E(x)=20 MeV with a width of 9 MeV. Distorted-wave Born approximation analysis on the angular distribution clearly indicated the L=2 multipolarity, attributing the E(x)=20 MeV state to the giant isovector quadrupole resonance.     

Alkylamines‐intercalated α‐zirconium phosphate as latent thermal anionic initiators

The reaction of glycidyl phenyl ether (GPE) with 1‐aminoalkanes‐intercalated α‐zirconium phosphate (α‐ZrP·1‐aminoalkane): 1‐aminoalkanes 1‐aminopropane (α‐ZrP·Pr), 1‐aminobutane (α‐ZrP·Bu), 1‐aminooctane (α‐ZrP·Oct), and 1‐aminohexadecane (α‐ZrP·Hed) was carried out at varying temperatures for 1 h periods. Reaction progress was not observed until the reactants were heated to 80 °C or above. On increasing the temperature, the conversion factors increased such that, at 140 °C, conversions of 62% (α‐ZrP·Pr), 60% (α‐ZrP·Bu), 67% (α‐ZrP·Oct), and 64% (α‐ZrP·Hed) were obtained. The thermal stabilities as latent initiators were tested: GPEs reacted with α‐ZrP·Pr, α‐ZrP·Bu, and α‐ZrP·Oct at 40 °C for 360 h achieved conversions of 83, 55, and 59%, respectively. In contrast, the reaction in the presence of α‐ZrP·Hed did not proceed at 40 °C. The order of the thermal stability of GPE in the presence of α‐ZrP·1‐aminoalkane intercalation compounds was: α‐ZrP·Hed > α‐ZrP·Bu ≈ α‐ZrP·Oct > α‐ZrP·Pr. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1854–1861     

Preparation of CF3-containing 1,3-di- and 1,1,3-trisubstituted allenes

Novel synthetic pathway to access trifluoromethylated allenes with 1,3-di- as well as 1,1,3-trisubstitution patterns was developed from a variety of 4,4,4-trifluorobut-2-yn-1-ols which were then transformed into the corresponding vinylic iodides in highly regio- and stereospecific manners, and zinc-mediated beta-elimination after trifluoroacetylation of the hydroxyl group eventually realized the formation of the target molecules in good to excellent overall yields in facile and short steps.     

Incorporation of glucose oxidase into Langmuir-Blodgett films based on Prussian blue applied to amperometric glucose biosensor

Glucose oxidase (GOx) was immobilized in the organic-inorganic Langmuir-Bldogett (LB) films consisting of octadecyltrimethylammonium (ODTA) and nanosized Prussian blue (PB) clusters. The amperometric glucose biosensors based on the LB films were fabricated and tested. It was found that the sensors exhibited a clear response current under an applied voltage of 0.0 V (vs Ag/AgCl). The linearity of current density versus glucose concentration was confirmed below 15 mmol/L concentration. This is the first observation of biosensor function of the hybrid organic-inorganic LB films. The successful preparation of glucose sensors operating at the very low potential indicates that the adsorbed PB clusters in the LB films act as an electrocatalyst for the electrochemical reduction of hydrogen peroxide, which is the final product of the enzymatic reaction sequence. The observed low potential applicability is estimated to inhibit the responses of interferants such as ascorbic acid, uric acid, and acetominophen. It was also found that an electrostatic interaction between positively charged ODTA+ and the adsorbed species of both GOx and PB provided a stabilized adsorption state in the LB films. Such stable immobilization contributes to the steady amperometric response current observed in the present ODTA/PB/GOx LB films.     

Quantitative assessment of regional systolic and diastolic functions and temporal heterogeneity of myocardial contraction in patients with myocardial infarction using cine magnetic resonance imaging and Fourier fitting

Purpose

The objective of this study is to determine regional left ventricle (LV) function and temporal heterogeneity of LV wall contraction by analyzing regional time–volume curve (TVC) after Fourier fitting and to assess altered systolic and diastolic functions and temporal indices of myocardial contraction in infarcted segments in comparison with noninfarcted myocardium in patients with myocardial infarction (MI).

Methods

Steady-state cine magnetic resonance (MR) and late gadolinium-enhanced (LGE) MR images were acquired using a 1.5-T MR system in 60 patients with MI. Regional LV function was determined by analyzing regional TVC in 16 segments. The fitted regional TVC was generated by Fourier curve fitting with five harmonics. Regional LV ejection fraction (EF), peak ejection rate (PER), peak filling rate (PFR), time to end-systole and time to peak filling (TPF) were determined from TVC and the first derivative curve.

Results

On LGE MR imaging (MRI), MI was observed in 307 of 960 segments (32.0%). Regional EF and PER averaged in LGE segments were 49.3±14.5% and 2.83±0.65 end-diastolic volume (EDV)/s, significantly lower than those in normal segments (66.7±11.9% and 3.63±0.60 EDV/s, P<.001 and P<.01, respectively). In addition, regional PFR, an index of diastolic function, was significantly reduced in LGE segments (1.94±0.54 vs. 2.86±0.68 EDV/s, P<.01). Time to end-systole and TPF were significantly greater in LGE segments (380.2±57.6 and 169.3±45.4 ms) than in normal segments (300.9±55.1 and 132.3±43.0 ms, P<.01 and P<.01, respectively).

Conclusions

Analysis of regional TVC on cine MRI after Fourier fitting allows quantitative assessment of regional systolic and diastolic LV functions and temporal heterogeneity of LV wall contraction in patients with MI.     

Thermoelectric power of quasi-one-dimensional Nb3X4 with X=S, Se andTe

The thermoelectric power of linear chain synthetic metals Nb₃X₄ (with X=S, Se and Te) was measured from 5 to 300 K. The thermopower is negative indicating a dominant transport by electrons. Common to three compounds, in lower temperature regions the thermopower rises linearly with temperature but soon saturates. With respect to Nb₃S₄ and Nb₃Se₄ we have found no special anomaly of the thermopower except for a little higher magnitude.With respect to Nb₃Te₄ anomalies in the thermopower vs temperature appear at about 80 and 20 K which are explained in terms of the charge- density-wave phase transition from the simultaneous measurement of the resistivity and the observation of the electron diffraction patterns.     

Rapid and Direct Conversion of Graphite Crystals into High‐Yielding,Good‐Quality Graphene by Supercritical Fluid Exfoliation

Graphene has attracted a great deal of attention in recent years due to its unusual electronic, mechanical, and thermal properties. Exploiting graphene properties in a variety of applications requires a chemical approach for the large‐scale production of high‐quality, processable graphene sheets (GS), which has remained an unanswered challenge. Herein, we report a rapid one‐pot supercritical fluid (SCF) exfoliation process for the production of high‐quality, large‐scale, and processable graphene for technological applications. Direct high‐yield conversion of graphite crystals to GS is possible under SCF conditions because of the high diffusivity and solvating power of SCFs, such as ethanol, N‐methyl‐pyrrolidone (NMP), and DMF. For the first time, we report a one‐pot direct conversion of graphite crystals to a high yield of graphene sheets in which about 90–95 % of the exfoliated sheets are <8 layers with approximately 6–10 % monolayers and the remaining 5–10 % are ≥10 layers.     

Stability of Bose-Einstein condensates in a double-well potential

We investigate the stability of the first excited state, the so-called “π-state,” of Bose-Einstein condensates in a double-well potential. From the condition of complex excitation energies, we determine the critical barrier height, above which the π-state is dynamically unstable. We find that the critical barrier height decreases monotonically as the number of condensate atoms increases. We also simulate the dynamics of the π-state by solving the time-dependent Gross-Pitaevskii equation. Our simulation results show that the π-state in the dynamically unstable region exhibits distinctively different behavior from that in the dynamically stable region.     

Homogenization problem for stochastic partial differential equations of Zakai type

We discuss homogenization for stochastic partial differential equations (SPDEs) of Zakai type with periodic coefficients appearing typically in nonlinear filtering problems. We prove such homogenization by two different approaches. One is rather analytic and the other is comparatively probabilistic.