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排序方式: 共有1165条查询结果,搜索用时 15 毫秒
71.
Hiroki Nara Shingo Tsuda Tetsuya Osaka 《Journal of Solid State Electrochemistry》2017,21(7):1925-1937
The development of lithium-sulfur batteries is associated with many problems. These problems include polysulfide dissolution, the shuttle phenomenon, the low electric and ionic conductivity of S, and the volume change that occurs during charge and discharge. In this review, various elemental techniques for overcoming these problems are summarized from the standpoints of the supporting materials. These techniques include preventing polysulfide dissolution from the cathodes through physical and chemical adsorption on the supporting materials, the use of electrolytes that do not dissolve polysulfides via the coordination of Li+ and solvents, and the use of ion-exchange polymers to permeate Li+ selectively. The following approaches to enable practical applications of S cathodes in future Li-ion batteries are introduced: the utilization of Li-free anode materials, such as C and Si; the use of Li2S cathodes, which are prepared via a pre-lithiation process; and increasing the areal capacity of the S cathode by using a suitable current collector such as Al foam, thus providing a large amount of space for Li+ to migrate and the electron-conductive path. The utilization of an Al foam current collector is one of the promising approaches to creating a cost-effective Li-ion battery owing to the established mass production of Al foam for use in NiMH batteries; such Li-ion battery can achieve an unprecedentedly high areal capacity of 21.9 mAh cm?2. Owing to the resulting areal capacity, the possibility of developing a lithium-sulfur battery with an energy density greater than 200 Wh kg?1 has been demonstrated. Consequently, the combination of these approaches, as introduced in this review, would help create a bright, sustainable society. 相似文献
72.
A convenient and one-pot synthetic method of lanthanide thiolate compounds was developed. An excess of metallic samarium, europium, and ytterbium directly reacted with diaryl disulfides in THF to give selectively Ln(II) thiolate complexes, [Ln(SAr)(&mgr;-SAr)(thf)(3)](2) (1, Ln = Sm; 2, Ln = Eu; Ar = 2,4,6-triisopropylphenyl), Yb(SAr)(2)(py)(4) (3, py = pyridine), and [{Ln(hmpa)(3)}(2)(&mgr;-SPh)(3)][SPh] (6, Ln = Sm; 7, Ln = Eu; 8, Ln = Yb; hmpa = hexamethylphosphoric triamide). Reaction of metallic lanthanides with 3 equiv of disulfides afforded Ln(III) thiolate complexes, Ln(SAr)(3)(py)(n)()(thf)(3)(-)(n)() (9a, Ln = Sm, n = 3; 9b, Ln = Sm, n = 2; 10, Ln = Yb, n = 3) and Ln(SPh)(3)(hmpa)(3) (11, Ln = Sm; 12, Ln = Eu; 13, Ln = Yb). Thus, Ln(II) and Ln(III) thiolate complexes were prepared from the same source by controlling the stoichiometry of the reactants. X-ray analysis of 8 revealed that 8 has the first ionic structure composed of triply bridged dinuclear cation and benezenethiolate anion [8, orthorhombic, space group P2(1)2(1)2(1) with a = 21.057(9), b = 25.963(7), c = 16.442(8) ?, V = 8988(5) ?(3), Z = 4, R = 0.040, R(w) = 0.039 for 5848 reflections with I > 3sigma(I) and 865 parameters]. The monomeric structures of 11 and 13 were revealed by X-ray crystallographic studies [11, triclinic, space group P&onemacr; with a = 14.719(3), b = 17.989(2), c = 11.344(2) ?, alpha = 97.91(1), beta = 110.30(2), gamma = 78.40(1) degrees, V = 2751.9(9) ?(3), Z = 2, R = 0.045, R(w) = 0.041 for 7111 reflections with I > 3sigma(I) and 536 parameters; 13, triclinic, space group P&onemacr; with a = 14.565(2), b = 17.961(2), c = 11.302(1) ?, alpha = 97.72(1), beta = 110.49(1), gamma = 78.37(1) degrees, V = 2706.0(7) ?(3), Z = 2, R = 0.031, R(w) = 0.035 for 9837 reflections with I > 3sigma(I) and 536 parameters]. A comparison with the reported mononuclear and dinuclear lanthanide thiolate complexes has been made to indicate that the Ln-S bonds weakened by the coordination of HMPA to lanthanide metals have ionic character. 相似文献
73.
Chun-Yang Jina Dao-Dao Zhang Tetsuya Oguma Shi-Xiong Qian 《Journal of inclusion phenomena and macrocyclic chemistry》1996,24(4):301-310
Cycloisomalto-heptaose (CI-7) and cycloisomalto-octaose (CI-8) are two novel cyclodextrans. Treatment with C60 or C70 by kneading leads to the formation of four distinct water-soluble inclusion complexes: CI-7/C60 (2: 1), CI-8/C60 (2: 1), CI-7/C70 (2: 1) and CI-8/C70 (2: 1). Their formation and structures have been examined by UV vis spectroscopy, X-ray powder diffraction and fluorescence spectral studies. The reaction is a reversible process. 相似文献
74.
Yoshihiko Ohishi Tomonori Kawabata Tetsuya Shishido Ken Takaki Qinghong Zhang Ye Wang Katsuomi Takehira 《Journal of molecular catalysis. A, Chemical》2005,230(1-2):49-58
M-MCM-41 catalysts (M: V, Cr, Fe, and Ga) prepared by direct hydrothermal synthesis (DHT) have been tested for dehydrogenation of ethylbenzene with CO2. The synthesized materials were characterized by X-ray diffraction (XRD), N2 adsorption (77 K), and diffuse reflectance UV–vis spectroscopic measurements. Cr-MCM-41 showed the highest activity among M-MCM-41 catalysts tested, resulting in the production of styrene with the conversion of 65% and the selectivity above 90%. The rate of styrene formation increased with increasing Cr loading up to 1.7 wt.%. It is suggested that Cr(VI)O4 in tetrahedral coordination is formed as an active monochromate species and reduced to Cr(III)O6 in octahedral coordination as a less active polychromate species during the reaction. Deactivated catalyst was regenerated by a treatment with gaseous oxygen or CO2, during which redistribution as well as reoxidation of polymeric Cr(III)O6 octahedra to monomeric Cr(VI)O4 tetrahedra was observed. The rate of CO formation increased together with that of styrene formation, while the rate of H2 formation decreased, with increasing partial pressure of CO2. It was confirmed that reverse water-gas shift reaction took place over Cr-MCM-41 by a separate experiment. The rate of CO formation during the dehydrogenation of ethylbenzene with CO2 over Cr-MCM-41 was well accounted for by assuming parallel occurrence of two reactions, i.e., direct oxidative dehydrogenation of ethylbenzene with CO2 and simple dehydrogenation of ethylbenzene thermodynamically assisted by reverse water-gas shift reaction. 相似文献
75.
Tetsuya Ezawa Seunghee Jung Yuya Kawashima Takuya Noguchi Nobuyuki Imai 《Tetrahedron: Asymmetry》2017,28(1):75-83
Dipeptides and amides were obtained in high yields from N-carbobenzyloxy α-amino acids and 3-phenylpropanoic acid with unprotected α-amino acids via the corresponding mixed carbonic carboxylic anhydrides using ethyl chloroformate and triethylamine by an ecological and convenient method in which the protection of C-terminals is not needed. 相似文献
76.
Mitsuru Ueda Tetsuya Abe Mitsuo Oda 《Journal of polymer science. Part A, Polymer chemistry》1992,30(9):1993-1998
Aromatic poly(thioether ketone)s were prepared by the direct polycondensation of aromatic dicarboxylic acids with aryl compounds containing ether or sulfide structures using phosphorus pentoxide/methanesulfonic acid (PPMA) as a condensing agent and solvent. Polycondensation proceeded smoothly and produced aromatic poly(thioether ketone)s with inherent viscosities up to 0.73 dL/g. The synthesis of substituted aryl ketones by the reaction of substituted benzoic acids with aryl compounds in PMMA was studied in detail to demonstrate the feasibility of the reaction for polymer formation. The thermogravimetry of the aromatic poly(thioether ketone)s showed a 10% weight loss in air and nitrogen at around 450 and 460°C, respectively. © 1992 John Wiley & Sons, Inc. 相似文献
77.
Tetsuya Hosaka 《Journal of Pure and Applied Algebra》2010,214(6):919-936
In this paper, we study CAT(0) groups and Coxeter groups whose boundaries are scrambled sets. Suppose that a group G acts geometrically (i.e. properly and cocompactly by isometries) on a proper CAT(0) space X. (Such a group G is called a CAT(0) group.) Then the group G acts by homeomorphisms on the boundary ∂X of X and we can define a metric d∂X on the boundary ∂X. The boundary ∂X is called a scrambled set if, for any α,β∈∂X with α≠β, (1) lim sup{d∂X(gα,gβ)∣g∈G}>0 and (2) lim inf{d∂X(gα,gβ)∣g∈G}=0. We investigate when boundaries of CAT(0) groups (and Coxeter groups) are scrambled sets. 相似文献
78.
Shoji Kasahara Tetsuya Takine Yutaka Takahashi Toshiharu Hasegawa 《Queueing Systems》1993,14(3-4):349-367
Many researchers have studied variants of queueing systems with vacations. Most of them have dealt with M/G/1 systems and have explicitly analyzed some of their performance measures, such as queue length, waiting time, and so on. Recently, studies on queueing systems whose arrival processes are not Poissonian have appeared. We consider a single server queueing system with multiple vacations and E-limited service discipline, where messages arrive to the system according to a switched Poisson process. First, we consider the joint probability density functions of the queue length and the elapsed service time or the elapsed vacation time. We derive the equations for these pdf's, which include a finite number of unknown values. Using Rouché's theorem, we determine the values from boundary conditions. Finally, we derive the transform of the stationary queue length distribution explicitly. 相似文献
79.
Tetsuya Abe 《Graphs and Combinatorics》2002,18(3):395-402
A pair (x,y) of elements in a lattice is mismatching if x is join-irreducible, y is meet-irreducible, and xy. The excess of a lattice L is defined by ex(L):=|L|− min{|V
x
|+|I
y
|:(x,y) is mismatching}, where V
x
(I
y
) is the principal filter (ideal) generated by x(y), respectively. In the first half of this paper, it is shown that a lattice has excess zero (one) if and only if it is isomorphic
to a Boolean lattice (one of a chain of length two, a diamond, and a pentagon), respectively. In the second half, we show
that for each relatively complemented lattice which is not Boolean, its size is at most five times its excess. Moreover we
determine extremal configurations.
Received: September 2, 1999 Final version received: July 25, 2000
Acknowledgments. The author thanks the referee for constructive comments.
Present address: Bureau of Human Resources, National Personnel Authority, 1-2-3 Kasumigaseki, Chiyoda-ku, Tokyo 100-8913, Japan. e-mail: abetet@jinji.go.jp 相似文献
80.