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排序方式: 共有498条查询结果,搜索用时 15 毫秒
491.
Keisuke Ohtani Philipp Gubler Makoto Oka 《The European Physical Journal A - Hadrons and Nuclei》2011,47(9):114
QCD sum rules of the nucleon channel are reanalyzed, using the maximum-entropy method (MEM). This new approach, based on the
Bayesian probability theory, does not restrict the spectral function to the usual “pole + continuum” form, allowing a more
flexible investigation of the nucleon spectral function. Making use of this flexibility, we are able to investigate the spectral
functions of various interpolating fields, finding that the nucleon ground state mainly couples to an operator containing
a scalar diquark. Moreover, we formulate the Gaussian sum rule for the nucleon channel and find that it is more suitable for
the MEM analysis to extract the nucleon pole in the region of its experimental value, while the Borel sum rule does not contain
enough information to clearly separate the nucleon pole from the continuum. 相似文献
492.
A. A. Kaminskii H. Rhee H. J. Eichler K. Ueda K. Oka H. Shibata 《Applied physics. B, Lasers and optics》2008,93(4):865-872
We report the experimental investigations of nonlinear-laser effects in LuVO4 vanadate under one-micron picosecond Nd3+:Y3Al5O12 pumping. In this tetragonal host-crystal for Ln3+ lasants for the first time we excited ultra-broad, more than one and half octave (13500 cm−1) Raman induced Stokes and anti-Stokes generation combs and observed multi-step cascaded parametric χ
(3)-lasing in UV spectral region. All generation lines were identified and attributed to SRS-promoting modes of the crystal (ω
SRS1≈900 cm−1 and ω
SRS2≈113 cm−1). We classified this vanadate as a promising material for self-Raman laser converters. 相似文献
493.
A Mueller matrix polarimeter acquired for four-channeled spectra is proposed. Both the polarizing and analyzing optics of this system consist of a linear polarizer and a high-order retarder. The polarizing elements can modulate the polarization states in the wavenumber space. By applying a Fourier transform method to a single-channeled spectrum, nine elements of the Mueller matrix can be deconvoluted without modifying the configuration of either the polarizing or analyzing optics. It is thus possible to determine the wavelength dependence of all the Mueller matrix elements from four-channeled spectra obtained using four different configurations for the polarizing and analyzing optics. The performance of this method is evaluated by measuring polarization properties, such as retardance, azimuthal angle, and linear diattenuation, from the obtained Mueller matrix in wavenumber space. 相似文献
494.
Kurt Dietliker Tunja Jung Johannes Benkhoff Hisatoshi Kura Akira Matsumoto Hidetaka Oka Daniela Hristova Georg Gescheidt Günther Rist 《Macromolecular Symposia》2004,217(1):77-98
New developments of photoinitiators are the base for the further extension of the radiation curing technology. Three different approaches are presented: The optimized combination of a bisacylphosphine oxide photoinitiator with a suitable stabilizer package allows the UV curing of clear coatings with an excellent performance in outdoor use. The design of new oxime ester derivatives allowed the introduction of a new tailor-made photoinitiator for color filter resists applications that considerably improves the color quality of the color filter. A novel photoinitiator class capable of releasing strong amine bases opens new opportunities for expanding radiation curing into resins types that crosslink by base-catalyzed processes. 相似文献
495.
Atsuyoshi Ohno Norimasa Yamazaki Akihiro Tsutsumi Yuji Mikata Mutsuo Okamura 《Heteroatom Chemistry》1995,6(1):51-56
2,3-Dihydro-2,2,4-trimethylthieno[3,2-b]pyridinium 1-oxide iodide ( 1 ) has been reacted with various inorganic and organic hydride donors. It has been found that the stereochemistry of reaction is controlled by the orientation of the sulfinyl dipole, and the relative bulkiness of substituents plays no role in determining the reaction face: a reactive hydride donor prefers to attack at the anti-face with respect to the sulfinyl dipole, whereas a less reactive hydride donor prefers to attack at the syn-face. 相似文献
496.
Yuki Oka Dr. Hiroshi Masai Prof. Dr. Jun Terao 《Angewandte Chemie (International ed. in English)》2023,62(14):e202217002
Catenanes with multistate switchable properties are promising components for next-generation molecular machines and supramolecular materials. Herein, we report a ligand-controlled switching method, a novel method for the multistate switching of catenanes controlled by complexation with added amine ligands. To verify this method, a [3]catenane comprising cyclic porphyrin dimers with a rigid π-system has been synthesized. Owing to the rigidity, the relative positions among the cyclic components of the [3]catenane can be precisely controlled by complexation with various amine ligands. Moreover, ligand-controlled multistate switching affects the optical properties of the [3]catenanes: the emission intensity can be tuned by modulating the sizes and coordination numbers of integrated amine ligands. This work shows the utility of using organic ligands for the structural switching of catenanes, and will contribute to the further development of multistate switchable mechanically interlocked molecules. 相似文献
497.
Ryota Akai Dr. Kouki Oka Naoki Okada Takahiro Ami Prof. Norimitsu Tohnai 《European journal of organic chemistry》2023,26(30):e202300417
Porous organic salts (POSs) are constructed through a strong charge-assisted hydrogen bond between sulfonic and amino groups. The molecular design of sulfonic acid, the linker part, enables various porous structures. In the current work, we synthesized p-terphenyl-4,4’’-disulfonic acid (TPDS), whose molecular structure can be easily modified by organic synthesis. Combining of TPDS and bulky tri-p-tolylmethanamine (TPMA-Me), which has three methyl groups at each para-position of the phenyl groups of triphenylmethylamine (TPMA), gave POS with one-dimensional pore channels having two different types of bottlenecks. The central benzene ring of TPDS is exposed on the surface of the pore. Therefore, we combined 4,4′-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzenesulfonic acid (BTDBS) containing 2,1,3-benzothiadiazole (BT) with TPMA-Me, and successfully constructed a one-dimensional pore channel with a bottleneck of 3.5 Å, by exposing BT to the surface of the pore. BTDBS/TPMA-Me exhibited a large adsorption/desorption hysteresis of nitrogen because of the bottleneck, electronic state of BT, and larger oxygen adsorption than the isostructural TPDS/TPMA-Me. Systematic and intended modulation of the pore structure of POS based on the modification of sulfonic acid was demonstrated, and for the first time, we established a precise design methodology for a one-dimensional pore channel with a bottleneck and high crystallinity in metal-free porous organic materials. 相似文献
498.