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131.
Imoto M Matsui Y Takeda M Tamaki A Taniguchi H Mizuno K Ikeda H 《The Journal of organic chemistry》2011,76(15):6356-6361
Observations show that nitroanilines exhibit an unusually high S(N)Ar reactivity with OH(-) in aqueous media in reactions that produce nitrophenols. S(N)Ar reaction of 4-nitroaniline (2a) in aqueous NaOH for 16 h yields 4-nitrophenol (4a) quantitatively, whereas a similar reaction of 4-nitrochlorobenzene (1a) gave 4a in 2% yield together with recovered 1a in 97%, suggesting that the leaving ability of the NH(2) group far surpasses that of Cl under these conditions. An essential feature of S(N)Ar reactions of nitroanilines is probably that the NH(2) leaving group participates in a hydrogen-bonding interaction with H(2)O. Density functional theory (DFT) calculations for a set of 4-nitroaniline, OH(-), and H(2)O suggest a possible formation of a Meisenheimer complex stabilized by hydrogen-bonding interactions and a six-membered ring structure. The results obtained here contrast with conventional S(N)Ar reactivity profiles in which nitroanilines are nearly unreactive with nucleophiles in organic solvents. 相似文献
132.
Rotational motion of a nitroxide radical, peroxylamine disulfonate (PADS), dissolved in room temperature ionic liquids (RTILs) was studied by analyzing electron paramagnetic resonance spectra of PADS in various RTILs. We determined physical properties of PADS such as the hyperfine coupling constant (A), the temperature dependence of anisotropic rotational correlation times (τ(∥) and τ(⊥)), and rotational anisotropy (N). We observed that the A values remain unchanged for various RTILs, which indicates negligible interaction between the N-O PADS group and the cation of RTIL. Large N values suggest strong interaction of the negative sulfonyl parts of PADS with the cations of RTILs. Most of the τ(∥), τ(⊥), and (τ(∥)τ(⊥))(1/2) values are within the range calculated on the basis of a hydrodynamic theory with stick and slip boundary conditions. It was deduced that this theory could not adequately explain the measured results in some RTILs with smaller BF(4) and PF(6) anions. 相似文献
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135.
Enomoto T Kanematsu S Tsunashima K Matsumoto K Hagiwara R 《Physical chemistry chemical physics : PCCP》2011,13(27):12536-12544
Fluorohydrogenate salts of quaternary phosphonium cations with alkyl and methoxy groups (tetraethylphosphonium (P(2222)(+)), triethyl-n-pentylphosphonium (P(2225)(+)), triethyl-n-octylphosphonium (P(2228)(+)), and triethylmethoxymethylphosphonium (P(222(101))(+))) have been synthesized by the metatheses of anhydrous hydrogen fluoride and the corresponding phosphonium bromide or chloride precursors. The three salts with asymmetric cations, P(222m)(FH)(2.1)F (m = 5, 8, and 101), are room temperature ionic liquids (ILs) and are characterized by differential scanning calorimetry, density, viscosity, and conductivity measurements. Linear sweep voltammetry using a glassy carbon working electrode shows these phosphonium fluorohydrogenate ILs have wide electrochemical windows (>4.9 V) with the lowest viscosity and highest conductivity in the known phosphonium-based ILs. Thermogravimetry shows their thermal stabilities are also improved compared to previously reported alkylammonium cation-based fluorohydrogenate salts. Differential scanning calorimetry and X-ray diffraction revealed that tetraethylphosphonium fluorohydrogenate salt, P(2222)(FH)(2)F, exhibits two plastic crystal phases. The high temperature phase has a hexagonal lattice, which is the first example of a plastic crystal phase with an inverse nickel arsenide-type structure, and the low-temperature phase has an orthorhombic lattice. The high-temperature plastic crystal phase exhibits a conductivity of 5 mS cm(-1) at 50 °C, which is the highest value for the neat plastic crystals. 相似文献
136.
Yokoi T Sakuma J Maeda K Domen K Tatsumi T Kondo JN 《Physical chemistry chemical physics : PCCP》2011,13(7):2563-2570
The confined space synthesis method has been applied to the preparation of sodium tantalate (NaTaO(3)); hydrothermal reaction of NaOH and Ta(2)O(5) was carried out in the pores of a three-dimensional mesoporous carbon, which was replicated by the colloidal array of silica nanospheres (SNSs) 20 nm in size. This approach led to the formation of a colloidal array of NaTaO(3) nanoparticles 20 nm in size with a surface area of 34 m(2) g(-1). The photocatalytic performance of the colloidal array of NaTaO(3) nanoparticles for overall water splitting under UV irradiation (λ > 200 nm) was evaluated after loading a NiO cocatalyst onto NaTaO(3) samples. The NiO-loaded NaTaO(3) nanoparticles showed photocatalytic activity for overall water splitting more than three times as high as non-structured bulk NaTaO(3) particles. 相似文献
137.
Kazuhiko Ogusu 《Optical and Quantum Electronics》1989,21(2):109-116
This paper presents a semi-analytical method for calculating the dispersion relationships for stationary non-linear TE waves guided by general multilayer waveguides with Kerr-like permittivities. The non-linear wave equations are solved rigorously for each layer, and the mode index and field distribution are systematically determined so as to satisfy the boundary conditions at all interfaces. To verify the validity of the present method, a non-linear graded-index waveguide is approximated by a number of step layers and the resultant multilayer waveguide is analysed numerically. The convergence properties of mode index and total power flow are presented, and these are compared with direct solutions of the non-linear wave equation by the numerical integration method. The dispersion relationships for a non-linear multiple-quantum-well waveguide have also been investigated under two simple permittivity models. The present method is useful for the analysis of non-linear graded-index waveguides in addition to non-linear multilayer waveguides such as the multiple-quantum-well structure. 相似文献
138.
Noriyuki Yonezawa Toshio Kanoe Kazuhiko Saigo Masaki Hasegawa 《Journal of polymer science. Part A, Polymer chemistry》1993,31(3):667-673
Two new types of polyamides having anti head-to-tail hydroxycinnamic acid dimer component in the main chain were synthesized. Their thermal degradation behavior was investigated by TG-DSC analysis in comparison with those of their model compounds and the polyamides derived from anti head-to-head coumarin dimer. The key reactions in the thermal degradation were clarified to be lactonization and cyclic imide formation. The polyamide, derived from 4-hydroxycinnamic acid dimer and hexamethylenediamine, showed good heat stability. © 1993 John Wiley & Sons, Inc. 相似文献
139.
Photochemical polar addition of alcohols to 1,1-diaryl-1,2,3-butatriene derivatives in the presence of a catalytic amount of 9,10-dicyanoanthracene regioselectively afforded 1,1-diaryl-4-alkoxy-1,2-butadienes as addition products in good yields via photoinduced electron transfer. 相似文献
140.
Kazuhiko Hosomi Toshihiko Fukamachi Hiroji Yamada Toshio Katsuyama Yasuhiko Arakawa 《Photonics and Nanostructures》2006,4(1):30-34
We demonstrate optical properties of one-dimensional photonic crystals (PC), which are fabricated using high-aspect-ratio etching on a V-grooved silicon wafer. The measured transmission spectrum has an obvious band gap; the suppression is over 30 dB. The quite small insertion loss of 1.9 dB is achieved by induced coupled plasma (ICP) cryogenic etching and direct coupling to the optical fiber aligned in the V-groove. We also successfully observed peaks originating from a localized cavity mode. Such a microcavity enables control of the light, which qualifies photonic crystal as a fundamental structure of optical functional devices. These results lead to achievement of integrated Si-based photonic circuits. 相似文献