Crystal and molecular structure of 6-0-acetylgrayanotoxin III

The crystal and molecular structure of a grayanotoxin III derivative, 6-0-acetylgrayanotoxin III is presented. The crystal is orthorhombic, space group P2₁2₁2₁, witha=15.582(3),b=21.304(3),c=6.339(3)Å,V=2104(1) ų Z=4. The structure was solved by direct methods and refined by full matrix least-squares methods to a finalR=0.047 for 1763 independent reflections withF ₀>3 (F ₀) The molecule is based on a tetracyclic structure consisting of two five-membered, one six-membered, and one seven-membered ring with various conformations.     

Curved Ferroelectric Liquid Crystal Matrix Displays Driven by Field-Sequential-Color and Active-Matrix Techniques

This paper describes a curved field-sequential-color matrix display using fast-response ferroelectric liquid crystal. Black matrix and transparent electrode patterns were formed on a thin plastic substrate by a transfer method from a glass substrate. While a composite film of liquid crystal and micro-polymers of walls and fibers was formed between the flexible substrates by printing, laminating and curing processes of a solution of monomers and liquid crystal, the mechanical stability was enhanced by use of multi-functional monomers to form large display panels. The image pixels of the matrix panel were driven by an active matrix scheme using an external switch transistor array at a frequency of 180 Hz for intermittent three-primary-color backlight illumination. The flexible A4-paper-sized color display with 24 × 16 pixels and 60 Hz field frequency was demonstrated by illuminating it with sequential three-primary-color lights from light-emitting diodes of the backlight. Our display system is useful in various information displays because of its freedom of setting and location.     

Single-molecule reaction and characterization by vibrational excitation

Controlled chemical reaction of single trans-2-butene molecules on the Pd(110) surface was realized by dosing tunneling electrons from the tip of a scanning tunneling microscope at 4.7 K. The reaction product was identified as a 1,3-butadiene molecule by inelastic electron tunneling spectroscopy. Threshold voltage for the reaction is approximately 365 mV, which coincides with the vibrational excitation of the C-H stretching mode. The reaction was ascertained to be caused by C-H bond dissociation by multiple vibrational excitations of the C-H stretching mode via inelastic electron tunneling process.     

Cloud and aerosol contributions to variation in shortwave surface irradiance over East Asia in July during 2001 and 2007

It is important to clarify the contributions of clouds and aerosols to the variation of surface shortwave irradiance (S) for climatological studies. This study examined the contributions of clouds and aerosols to the variation in S over East Asia (75-135°E, 20-55°N) in July during 2001 and 2007 using the index of potential radiative forcing (PRF) to characterize the temporal and geographical variations. After confirming the validity of PRF for multiyear analyses, we performed several temporal analyses of clouds and aerosols over the whole research domain. Changes in the geographical distribution, contribution histograms, and averaged values were studied. In agreement with previous studies that treated single-year cases, we confirmed that the magnitudes of the temporal changes in S variations due to clouds and aerosols were highly variable geographically. As for domain-averaged S variations, we did not observe defined trends for the research period. It was also found that the temporal variation between one parameter and its S variation was negatively correlated, from the point analyses at two locations. Based on these results, we concluded that PRF is a promising tool for research into long-term S variations. This kind of information will be quite valuable as basic data for use in climate modeling.     

Fast Encoding Method for Image Vector Quantization Based on Multiple Appropriate Features to Estimate Euclidean Distance

The encoding process of finding the best-matched codeword (winner) for a certain input vector in image vector quantization (VQ) is computationally very expensive due to a lot of k-dimensional Euclidean distance computations. In order to speed up the VQ encoding process, it is beneficial to firstly estimate how large the Euclidean distance is between the input vector and a candidate codeword by using appropriate low dimensional features of a vector instead of an immediate Euclidean distance computation. If the estimated Euclidean distance is large enough, it implies that the current candidate codeword could not be a winner so that it can be rejected safely and thus avoid actual Euclidean distance computation. Sum (1-D), L₂ norm (1-D) and partial sums (2-D) of a vector are used together as the appropriate features in this paper because they are the first three simplest features. Then, four estimations of Euclidean distance between the input vector and a codeword are connected to each other by the Cauchy–Schwarz inequality to realize codeword rejection. For typical standard images with very different details (Lena, F-16, Pepper and Baboon), the final remaining must-do actual Euclidean distance computations can be eliminated obviously and the total computational cost including all overhead can also be reduced obviously compared to the state-of-the-art EEENNS method meanwhile keeping a full search (FS) equivalent PSNR.     

M?ssbauer spectroscopic study on valence-detrapping and trapping of mixed-valence trinuclear iron(III, III, II) fluorine-substituted benzoate complexes

Magnetorheological (MR) fluids are new iron-based materials, whose applications include brakes, dampers, clutches, shock absorbers systems and polishing of optical surfaces (lens and mirrors). They are dependent on the size and shape of particles as the magnetic properties. Interested in the possibility of using iron-rich powders, commonly used in nondestructive testing, ranging in size from a few μm to about 200?μm and lower cost than those commercially used for MR fluids, a study of the structural and magnetic properties of iron-rich metallic particles by X-ray diffraction (XRD) and M?ssbauer spectroscopy (MS) at room temperature has been done. Powders, as received, were separated into particle sizes smaller than 20?μm (sample A) and in the range of 20–38?μm (sample B) because these are the sizes generally required for applications in MR fluids. The particles whose sizes exceed the above values were ground in a high energy planetary mill for 3?h, using different values of rotational speed/time: 200?rpm for one hour, a pause of 10?s, 140?rpm for one hour, pause 10?s and then 175?rpm during the last hour. These powders were sieved to obtain particles smaller than 20?μm (sample C). According XRD results, in all samples, only α-Fe (lattice parameter a = 2,867(2) ?) and Fe₂O₃ (lattice parameter a = 5,037(1) ? and c = 13,755(8) ?) were present. The M?ssbauer spectra were fitted with two sextets. The hyperfine parameters values allowed us to assign the highest relative area spectrum (sextet) corresponding to α-Fe and the second one to Fe₂O₃ in accord to the XRD results. Thus, the preparation method using mechanical milling for diminishing the size of the metallic particles allowed us to get particles with size and magnetic properties that could lead to potentially MR fluids applications.