Observation of a new absorption due to a precursor of the lowest triplet state of 1,8-dichloroanthraquinone

The buildup and decay of a new absorption of 1,8-dichloroanthraquinone was observed on the picosecond time scale. Since the decay of this absorption was accompanied by a rate matching increase in the T′  T₁ absorption, the new absorption was assigned to a precursor of the lowest triplet state of 1,8-dichloroanthraquinone     

Structure and stereochemistry of boschniakine, boschnialactone, and boschnialinic acid, an oxidation product of boschnialactone

Boschniakine, C₁₀H₁₁NO, and boschnialactone, C₉H₁₄O₂, were isolated as the physiologically active principles of Boschniakia rossica Hunt, and their absolute structures have been determined. Four optically active stereoisomers of boschnialinic acid (2-carboxy-3-methylcyclopentylacetic acid), one of which is an oxidation product of boschnialactone, have been synthesized and their stereochemistries established.     

High sensitivity search for nu;e's from the sun and other sources at KamLAND

Data corresponding to a KamLAND detector exposure of 0.28 kton yr has been used to search for nu;(e)'s in the energy range 8.3相似文献   

High-resolution transmission electron microscopy study of Ca(3)Co(4)O(9)

The crystal structure of Ca(3)Co(4)O(9) was investigated using high-resolution transmission electron microscopy (HRTEM) and the image-simulation method. The c(*) was 10.8A and the b parameters were 4.56A for the Ca(2)CoO(3) block and 2.82A for the CoO(2) sheet. The [110] zone axis HRTEM images confirmed that Ca(3)Co(4)O(9) has a modulated layered structure with modulation. For the first time, the atomic positions of the Ca and Co atoms in the Ca(2)CoO(3) block were identified, corresponding to three rows of dark spots in the [110] direction. The observed HRTEM images for Ca(2)CoO(3) agreed well with the calculated images based on the structural model obtained by the Rietveld refinement method.     

Improvement of depth position in 2-D/3-D registration of knee implants using single-plane fluoroscopy

Two-dimensional (2-D)/three-dimensional (3-D) registration techniques using single-plane fluoroscopy are highly important for analyzing 3-D kinematics in applications such as total knee arthroplasty (TKA) implants. The accuracy of single-plane fluoroscopy-based techniques in the determination of translation perpendicular to the image plane (depth position), however, is relatively poor because a change in the depth position causes only small changes in the 2-D silhouette. Accuracies achieved in depth position using conventional 2-D/3-D registration techniques are insufficient for clinical applications. Therefore, we propose a technique for improving the accuracy of depth position determination in order to develop a system for analyzing knee kinematics over the full six degrees of freedom (6 DOF) using single-plane fluoroscopy. In preliminary experiments, the behaviors of errors for each free variable were quantified as evaluation curves by examining changes in cost function with variations in the free variable. The evaluation curve for depth position was more jagged, and the curve peak less pointy, compared to the evaluation curves of the other five variables, and the curve was found to behave differently. Depth position is therefore optimized independently of the other variables, using an approximate evaluation curve of depth position prepared after initial registration. Accuracy of the proposed technique was evaluated by computer simulation and in vitro tests, with validation of absolute position and orientation performed for each knee component. In computer simulation tests, root-mean-square error (RMSE) in depth position was improved from 2.6 mm (conventional) to 0.9 mm (proposed), whereas for in vitro tests, RMSE improved from 3.2 mm to 1.4 mm. Accuracy of the estimation of the remaining two translational and three rotational variables was found to be almost the same as that obtained by conventional techniques. Results of in vivo tests are also described in which the possibility of full 6 DOF kinematic analysis of TKA implants is shown.     

Simultaneous determination of water-soluble vitamins in a vitamin-enriched drink by an in-capillary enzyme reaction method

The in-capillary enzyme reaction method was used to determine riboflavin phosphate in a vitamin-enriched drink based on its conversion to riboflavin (vitamin B2) with alkaline phosphatase. Simultaneously, three water-soluble vitamins [thiamine nitrate (vitamin B2 mononitrate), pyridoxine hydrochloride (vitamin B6 hydrochloride) and nicotinamide (vitamin PP)] and anhydrous caffeine in the drink were subjected to quantitative analysis. In the system, electrophoretic migration was used to mix zones containing the substrate (riboflavin phosphate) and the enzyme (alkaline phosphatase). The reaction was then allowed to proceed in the presence of a weak electric field and, finally, the product (riboflavin) of enzyme reaction and other water-soluble vitamins migrated under the influence of an applied electric field to the detector. All the active ingredients and the formulation excipients were successfully separated by micellar electrokinetic chromatography with 135 mM sodium dodecyl sulfate. To prevent inhibition of enzyme reaction by the addition of sodium dodecyl sulfate to the reaction zone, sandwich mode injection, in which plugs of sandwich solution without sodium dodecyl sulfate were introduced into the capillary on both sides of the reaction zone, was utilized as a barrier to protect the enzyme reaction from the inhibitor. The relationship between the peak area of the product and the concentration of the substrate was calculated in the in-capillary enzyme reaction method. Excellent linearity was obtained, with correlation coefficients of 0.9999. The established method was validated and demonstrated to be applicable to the determination of the five active ingredients, including riboflavin phosphate, in a commercial vitamin-enriched drink. No interference from the formulation excipients was observed. Good linearities were obtained, with correlation coefficients above 0.999. Recoveries and precisions ranged from 99.3 to 101.8%, and from 0.1 to 2.5% RSD, respectively. Good agreement was obtained between the established method and traditional high-performance liquid chromatographic methods. These results suggest that the in-capillary enzyme reaction method can be used for the simultaneous determination of riboflavin phosphate and other water-soluble vitamins in pharmaceuticals.     

Survivable MPLS Over Optical Transport Networks: Cost and Resource Usage Analysis

In this paper we study different options for the survivability implementation in MPLS over optical transport networks (OTN) in terms of network resource usage and configuration cost. We investigate two approaches to the survivability deployment: single layer and multilayer survivability and present various methods for spare capacity allocation (SCA) to reroute disrupted traffic. The comparative analysis shows the influence of the offered traffic granularity and the physical network structure on the survivability cost: for high bandwidth LSPs, close to the optical channel capacity, the multilayer survivability outperforms the single layer one, whereas for low bandwidth LSPs the single layer survivability is more cost-efficient. On the other hand, sparse networks of low connectivity parameter use more wavelengths for optical path routing and increase the configuration cost, as compared with dense networks. We demonstrate that by mapping efficiently the spare capacity of the MPLS layer onto the resources of the optical layer one can achieve up to 22% savings in the total configuration cost and up to 37% in the optical layer cost. Further savings (up to 9 %) in the wavelength use can be obtained with the integrated approach to network configuration over the sequential one, however, at the increase in the optimization problem complexity. These results are based on a cost model with different cost variations, and were obtained for networks targeted to a nationwide coverage     

Quantitative on‐line concentration for capillary electrophoresis with inkjet sample introduction technique

A quantitative sample introduction method based upon inkjet injection was applied to capillary electrophoresis coupled with stacking and sweeping on‐line concentration techniques. Methylxanthines were used as model compounds for the proof‐of‐concept of the method. The volume of injected sample could be easily manipulated by controlling the number of ejected droplets in the injection procedure. Under optimized conditions, a linear relationship between the ejected droplet number and peak area was obtained when the droplet number introduced into the capillary was less than 100. Under optimized quantitative on‐line concentration conditions, the limits of detection for theobromine, caffeine, and theophylline were 1.0, 2.0, and 1.0 μM, respectively. The inkjet injection system was evaluated by comparing it with conventional injection methods. The electropherogram of the inkjet injection mode was the same as that for hydrodynamic injection mode, and no sample discrimination was observed compared with the electrokinetic injection mode. The established method was applied to the determination of methylxanthines in bottled green tea. The recoveries of theobromine, caffeine, and theophylline were 94.1, 110.6, and 86.8%, respectively. We conclude that proposed method can be used for quantitative concentration for capillary electrophoresis, thus resulting in an improved accuracy.     

Investigation of ultrafast nuclear spin polarization induced by short laser pulses

We theoretically investigate the dynamics of nuclear spin induced by short laser pulses and show that ultrafast nuclear spin polarization can take place. Combined use of the hyperfine interaction together with the static electric field is the key for that. Specifically we apply the idea to unstable isotopes, (27)Mg and (37)Ca, with nuclear spin of 1/2 and 3/2, respectively, and show that 88% and 62% of nuclear spin polarization can be achieved within a few to tens of ns, which is 2-3 orders of magnitude shorter than the time needed for any known optical methods. Because of its ultrafast nature, our scheme would be very effective not only for stable nuclei but also unstable nuclei with a lifetime as short as mus.