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21.
Fundamental mechanism of femtosecond-laser-induced periodic surface nanostructure formation has been investigated under the condition using superimposed multiple shots at lower fluence than the single-pulse ablation threshold. With increasing the shot number of low-fluence fs-laser pulses, the periodic nanostructure develops through the bonding structure change of target material, the nanoscale ablation with optical near-fields induced around the high curvatures, and the excitation of surface plasmon polaritons (SPPs) to create the nano-periodicity in the surface structure. It is confirmed that non-thermal interaction at the surface plays the crucial role in the nanostructure formation. Based on the mechanism, we have demonstrated that the periodic nanostructure formation process can be controlled to fabricate a homogeneous nanograting on the target surface, using a two-step ablation process in air. The experimental results obtained represent exactly the nature of a single spatial standing SPP wave mode that generates periodically enhanced near-fields for the nanograting formation. The calculated results for a model target reproduce well the nanograting period and explain the characteristic properties observed in the experiment. 相似文献
22.
Keitaro Tanoi Natsuko I. Kobayashi Takayuki Saito Naoko Iwata Atsushi Hirose Yoshimi Ohmae Ren Iwata Hisashi Suzuki Tomoko M. Nakanishi 《Journal of Radioanalytical and Nuclear Chemistry》2013,296(2):749-751
The time course of Mg uptake and release using intact rice plants and 28Mg as a tracer is presented. Since there is no conventional Mg tracer available, 28Mg was produced via 27Al(α, 3p)28Mg reaction using a cyclotron. Using the purified 28Mg tracer, it was found that the uptake amount of 28Mg by the rice plants increased linearly during 30 min of application. After 28Mg treatment for 90 min, the roots were sequentially washed with iced solution for 120 min. Within about 10 min, almost all of the 28Mg, that was thought to be weakly bound to the apoplast, was washed away. 相似文献
23.
An automatic aberration correction method has been implemented in scanning electron microscopes (SEM). Necessity of the automatic aberration correction is discussed. The procedure of the automatic aberration correction is explained in detail, where deconvolution techniques are used in order to extract probe information from SEM images. Due to the precise digitization and the usage of proper combinations of correction fields, linearity has been found between the amplitude of each aberration and the corresponding field strength. Experimental results are shown which demonstrate that the aberrations are corrected automatically by a linear feedback control method. After the automatic aberration correction, the image quality has been improved drastically. 相似文献
24.
Measurements of rate constants and substituent effects for three important elementary steps of proton-transfer reactions of phenylnitromethane were reported. The Hammett ρ values for the deprotonation of ArCH(2)NO(2) with OH(-), protonation of ArCH═NO(2)(-) with H(2)O, and protonation of ArCH═NO(2)(-) with HCl were determined in aqueous MeOH at 25 °C. Comparison of these experimentally observed ρ values with those calculated at B3LYP/6-31G* revealed that aci-nitro species (ArCH═NO(2)H), which is formed on the O-protonation of ArCH═NO(2)(-), does not lie on the main route of the proton-transfer reaction. Analysis of the Br?nsted plot implies that the proton-transfer reaction of most XC(6)H(4)CH(2)NO(2) exhibits nitroalkane anomaly, but not for p-NO(2)C(6)H(4)CH(2)NO(2), and that the transition state charge imbalance is an origin of anomaly. 相似文献
25.
Dr. Yoshihiro Sohtome Bongki Shin Natsuko Horitsugi Prof. Dr. Keiichi Noguchi Prof. Dr. Kazuo Nagasawa 《化学:亚洲杂志》2011,6(9):2463-2470
Herein, we present details of our conformationally flexible, 1,3‐diamine‐tethered guanidine/bisthiourea organocatalysts for chemo‐, regio‐, and enantioselective 1,4‐type Friedel–Crafts reactions of phenols. These organocatalysts show a unique stereo‐discrimination governed by the differential activation entropy (ΔΔS≠), rather than by the differential activation enthalpy (ΔΔH≠). Extensive kinetic analyses using Eyring plots for a series of guanidine/bisthiourea organocatalysts revealed the key structural motif in the catalysts associated with a large magnitude of differential activation entropy (ΔΔS≠). A plausible guanidine–thiourea cooperative mechanism for the enantioselective Friedel–Crafts reaction is proposed. 相似文献
26.
27.
Hideki Miyaji Takanao Asahi Yoshihisa Miyamoto Kenjiro Asai 《Journal of Polymer Science.Polymer Physics》1987,25(1):159-171
Lattice constants of the monoclinic form of polyethylene under pressures up to 1.8 GPa at 298 K are investigated by x-ray diffraction. The thermal expansion from 100 K to 300 K at atmospheric pressure is also studied. The equation of state is calculated by Pastine's method, taking into account the zero-point vibration, and is compared with experimental results. The calculated results depend largely on the interatomic potential used and the limit of the interatomic distance for summation of the potentials. A change in the angle γ between the a and b axes results in an anisotropic change in the unit cell dimension with both pressure and temperature; the a and b axes change at nearly the same rate. The monoclinic form may have a higher density than the orthorhombic form at pressures above 1.0 GPa. 相似文献
28.
Katsuaki Miyaji Toshio Nakamura Hiroshi Hirota Michito Igarashi Takeyoshi Takahashi 《Tetrahedron letters》1984,25(46):5299-5302
12β-Hydroxypicrasan-3-one, a compound having the correct relative stereochemistry of all the six ring-juncture chiral centers of the picrasane skeleton, was synthesized from a known tricyclic compound, using the orthoester Claisen rearrangement and lead tetraacetate oxidation as key reactions. 相似文献
29.
High-order harmonic generation from coherently rotating N2 and O2 molecules has been observed for different alignment angles in a pump and probe experiment using femtosecond laser pulses. The results obtained are in excellent agreement with those calculated using a recently developed theory, which represent the characteristic properties predicted for angle-dependent harmonic generation. It is shown that polarization geometry and alignment distribution play essential roles in potential applications to probe electronic structure and dynamics of molecular systems. 相似文献
30.
Direct Estimation of the Surface Location of Immobilized Functional Groups for Concerted Catalysis Using a Probe Molecule 下载免费PDF全文
Hiroto Noda Dr. Ken Motokura Prof. Dr. Yusuke Wakabayashi Kaori Sasaki Dr. Hiroo Tajiri Dr. Akimitsu Miyaji Dr. Sho Yamaguchi Prof. Dr. Toshihide Baba 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(15):5113-5117
The location of active sites during concerted catalysis by a metal complex and tertiary amine on a SiO2 surface is discussed based on the interaction between the functionalized SiO2 surface and a probe molecule, p‐formyl phenylboronic acid. The interactions of the probe molecule with the surface functionalities, diamine ligand, and tertiary amine, were analyzed by FT‐IR and solid‐state 13C and 11B MAS NMR. For the catalyst exhibiting high 1,4‐addition activity, the diamine ligand and tertiary amine base exist in closer proximity than in the catalyst with low activity. 相似文献