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131.
Dr. Jun Nakazawa Tomoaki Hori Prof. Dr. T. Daniel P. Stack Prof. Dr. Shiro Hikichi 《化学:亚洲杂志》2013,8(6):1191-1199
Immobilized nickel catalysts SBA*‐ L ‐x/Ni ( L =bis(2‐pyridylmethyl)(1H‐1,2,3‐triazol‐4‐ylmethyl)amine) with various ligand densities ( L content (x)=0.5, 1, 2, 4 mol % Si) have been prepared from azidopropyl‐functionalized mesoporous silicas SBA‐N3‐x. Related homogeneous ligand LtBu and its NiII complexes, [Ni( LtBu )(OAc)2(H2O)] ( LtBu /Ni) and [Ni( LtBu )2]BF4 (2 LtBu /Ni), have been synthesized. The L /Ni ratio (0.9–1.7:1) in SBA*‐ L ‐x/Ni suggests the formation of an inert [Ni L 2] site on the surface at higher ligand loadings. SBA*‐ L ‐x/Ni has been applied to the catalytic oxidation of cyclohexane with m‐chloroperbenzoic acid (mCPBA). The catalyst with the lowest loading shows high activity in its initial use as the homogeneous LtBu /Ni catalyst, with some metal leaching. As the ligand loading increases, the activity and Ni leaching are suppressed. The importance of site‐density control for the development of immobilized catalysts has been demonstrated. 相似文献
132.
Magnetic phase transition in a heteromolecular hydrogen-bonded complex of nitronylnitroxide radicals
Hayakawa K Shiomi D Ise T Sato K Takui T 《The journal of physical chemistry. B》2005,109(19):9195-9197
An organic molecular acid-base complex has been synthesized from pyridine-substituted biradical 2 in a triplet (S = 1) ground state and a benzoic acid derivative of monoradical 3 with S = 1/2. The two constituent molecules are bound by an OH-N hydrogen bond in a crystalline solid state. The complex has been found to exhibit an antiferromagnetic phase transition at 5 K. The complex is the first example of a hydrogen-bonded heterospin, heteromolecular complex exhibiting a magnetic phase transition in purely organic molecule-based materials. 相似文献
133.
Matos JR Kruk M Mercuri LP Jaroniec M Zhao L Kamiyama T Terasaki O Pinnavaia TJ Liu Y 《Journal of the American Chemical Society》2003,125(3):821-829
FDU-1 silicas with large cage-like pores (diameter about 10 nm) were synthesized under acidic conditions from tetraethyl orthosilicate in the presence of a poly(ethylene oxide)-poly(butylene oxide)-poly(ethylene oxide) triblock copolymer template B50-6600 (EO(39)BO(47)EO(39)). High-resolution transmission electron microscopy and small-angle X-ray scattering provided strong evidence that FDU-1 silica synthesized under typical conditions is a face-centered cubic Fm3m structure with 3-dimensional hexagonal intergrowth and is not a body-centered cubic Im3m structure, as originally reported. Samples synthesized in a wide range of conditions (initial temperatures from 298 to 353 K; hydrothermal treatment at 333-393 K) exhibited similar XRD patterns and their nitrogen adsorption isotherms indicated a good-quality cage-like pore structure. The examination of low-pressure nitrogen adsorption isotherms for FDU-1 samples, whose pore entrance diameters were evaluated using an independent method, allowed us to conclude that low-pressure adsorption was appreciably stronger for samples with smaller pore entrance sizes. This prompted us to examine low-pressure adsorption isotherms for a wide range of samples and led us to a conclusion that the FDU-1 pore entrance size can be systematically enlarged from about 1.3 nm (perhaps even lower) to at least 2.4 nm without an appreciable loss of uniformity by increasing the temperature of the hydrothermal treatment or the initial synthesis. Further enlargement of pore entrance size was achieved for sufficiently long hydrothermal treatment times at temperatures of 373 K or higher, as seen from the shape of nitrogen desorption isotherms. This allowed us to obtain samples with uniform pore sizes, high adsorption capacity, and with pore entrances enlarged so much that their size was similar to the size of the pore itself, resulting in a highly open porous structure. However, in the latter case, there was evidence that the pore entrance size distribution was quite broad. 相似文献
134.
Tomoaki Seyama Toshifumi Tanimura Keigo Tashiro Suzuko Yamazaki 《Research on Chemical Intermediates》2017,43(9):5025-5039
Porous platinum ion-doped TiO2 (Pt–TiO2) was prepared by a sol–gel method and demonstrated to have superior photocatalytic activity for the photodegradation of gaseous trichloroethylene (TCE) under visible light (VL) irradiation from a xenon lamp equipped with 422-nm cut-off filter. Kinetic studies were performed to clarify the effect of the doping amounts, space times, VL intensity, and mole fractions of TCE, O2, and H2O on the degradation of TCE. Under ultraviolet (UV) irradiation, the photocatalytic activity of Pt–TiO2 was the same as that of TiO2, indicating that the doped Pt ion did not act as a recombination center for the photogenerated holes and electrons. Based on the kinetic data and reaction products, we conclude that the photocatalytic degradation of TCE on Pt–TiO2 under VL irradiation proceeds similarly to TiO2 under UV irradiation. We also performed the photocatalytic degradation of TCE at the space time of 7.5 × 107 g s mol?1 in a tubular reactor packed with the Pt–TiO2 pellets which are more suitable than the Pt–TiO2 powder for the practical remediation of the contaminated gas. TCE was completely degraded, i.e. 100% conversion was achieved under VL irradiation but only a small quantity of CO2 was formed with the stoichiometric ratio of [CO2]formed/[TCE]degraded of ca. 0.33. By switching the gas stream containing TCE to humid air, more CO2 was formed, indicating that the dichloroacetates accumulated on the Pt–TiO2 surface are photodegradable to CO2 under VL irradiation. 相似文献
135.
Tomooki Hosaka Tomoaki Shimamura Kei Kubota Shinichi Komaba 《Chemical record (New York, N.Y.)》2019,19(4):735-745
Lithium‐ion batteries have the highest energy density among practical secondary batteries and are widely used for electronic devices, electric vehicles, and even stationary energy‐storage systems. Along with the expansion of demand and applications, the concern about resources of lithium and cobalt is growing. Therefore, secondary batteries composed of abundant elements are required to complement lithium‐ion batteries. In recent years, the development of potassium‐ion batteries has attracted much attention, especially for large‐scale energy storage. In order to realize potassium‐ion batteries, various compounds are proposed and investigated as positive electrode materials, including layered transition‐metal oxides, Prussian blue analogues, and polyanionic compounds. This article offers a review of polyanionic compounds which are typically composed of abundant elements and expected high operating potential. Furthermore, we deliver our new results to partially compensate for lack of studies and provide a future perspective. 相似文献
136.
Ichiro Seto Tomoaki Ohtsuki Iwao Sasase Shinsaku Mori 《Fiber and Integrated Optics》1993,12(4):381-395
We propose a Polarization Shift Keying (POLSK) phase diversity homo-dyne system with multiplying detection in coherent optical communications. The proposed system uses only one of three Stokes parameters, which is the phase difference between two orthogonal polarizations. Although such systems using only one Stokes parameter are very sensitive to polarization fluctuation, the proposed system becomes insensitive to the linear polarization fluctuation by using the multiplying detection with a combination of in-phase and quadrature optical signal components on two orthogonal polarizations. Furthermore, insensitivity to phase noise and offset frequency and attractiveness due to homodyne type in high-speed transmissions are maintained. The most attractive feature of the proposed system is that neither a polarization controller nor electronic feedback loop for matching the state of polarization (SOP) between transmitted and local oscillator (LO) optical signals is needed. We theoretically analyze the receiver sensitivity and the power penalties of the proposed system for the cases of the elliptical SOP of received optical signals and the imbalance optical 90° hybrid. 相似文献
137.
CuIn(SxSe1−x)2 thin polycrystalline films were grown by the chemical spray pyrolysis method on the glass substrate at 280-400°C. The alloy composition in the film was studied with relation to that in the splay solution. Films were characterized by X-ray diffraction, optical absorption, Raman spectroscopy, resistivity and surface morphology. The CuInSe2-rich alloy films grown at high substrate temperature had chalcopyrite structure, while, the CuInS2-rich films grown at low substrate temperature exhibited sphalerite structure. Optical-gap energies were smaller than that of the bulk crystal by 0.1-0.2 eV for CuInS2-rich films. Raman spectra exhibited both CuInSe2-like and CuInS2-like A1 modes, and their relative changed systematically with alloy composition. 相似文献
138.
Satoru Utsugi Yoshitaka Ehara Hidenori Tanaka Tomoaki Yamada Hiroshi Funakubo Hiroshi Uchida 《Journal of Crystal Growth》2010,312(21):3127-3130
Epitaxial (La0.07Sr0.93)SnO3 [LSSO] films were deposited on CaF2 substrates by pulse laser deposition. The (1 0 0)c orientation of LSSO films was observed only on (1 1 0)CaF2, whereas (1 1 0)c orientation was found on (1 1 1)CaF2 and (1 0 0)CaF2. (0 0 1) polar axis oriented tetragonal Pb(Zr0.35Ti0.65)O3 films were grown on the fabricated (1 0 0)cLSSO∥(1 1 0)CaF2 by pulsed metal organic chemical vapor deposition. The (0 0 1)Pb(Zr0.35Ti0.65)O3∥(1 0 0)cLSSO∥(1 1 0)CaF2 stack structure exhibited about 70% transparency with an adsorption edge of approximately 330 nm. 相似文献
139.
Hirashita T Kamei T Satake M Horie T Shimizu H Araki S 《Organic & biomolecular chemistry》2003,1(21):3799-3803
Diastereoselective couplings of salicylaldehyde, anisaldehyde and 2-pyridylaldehyde with crotyl- and cinnamylindium reagents were studied. The syl/anti selectivity was found to depend largely on the ligands on the indium atom of the allylic indium reagents. A syn-selective cinnamylation of salicylaldehyde was realized by the combination of cinnamyl acetate and indium(I) iodide, whereas an anti-selective coupling with salicylaldehyde was achieved by the indium trichloride/aluminium-mediated cinnamylation. 相似文献
140.
Tomoaki Sugiyama Hiroya Shiba Dr. Masashi Yoshikawa Prof. Dr. Hiroaki Wada Prof. Dr. Atsushi Shimojima Prof. Dr. Kazuyuki Kuroda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(11):2764-2772
The controlled synthesis of oligosiloxanes with well-defined structures is important for the bottom-up design of siloxane-based nanomaterials. This work reports the synthesis of various polycyclic and cage siloxanes by the hydrolysis and intramolecular condensation of monocyclic tetra- and hexasiloxanes functionalized with various alkoxysilyl groups. An investigation of monoalkoxysilylated cyclosiloxanes revealed that intramolecular condensation occurred preferentially between adjacent alkoxysilyl groups to form new tetrasiloxane rings. The study of dialkoxy- and trialkoxysilylated cyclotetrasiloxanes revealed multistep intramolecular condensation reactions to form cubic octasiloxanes in relatively high yields. Unlike conventional methods starting from organosilane monomers, intramolecular condensation enables the introduction of different organic substituents in controlled arrangements. So-called Janus cubes have been successfully obtained, that is, Ph4R4Si8O12, in which R=Me, OSiMe3, and OSiMe2Vi (Vi=vinyl). These findings will enable the creation of siloxane-based materials with diverse functions. 相似文献