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161.
The goal of this work was the development of a novel type of heterogeneous catalyst, consisting of bare metal nanoparticles
on stainless steel foils, which can be shaped to any kind of architecture and, if necessary, heated electrically. Solutions
of pre-prepared, ligand protected and monodispersed gold, palladium, platinum and rhodium nanoparticles were sprayed onto
stainless steel foils, followed by the careful removal of the ligand molecules by an oxygen plasma treatment. Due to this,
bare particles become irreversibly fixed on the steel support. It could be shown that the original particle sizes do not change
during the plasma treatment. Foils, densely coated with the nanoparticles, were used for gas phase catalyses in a self-made
reactor at room temperature or at 60 °C. Hydrogenation of 1,3-butadiene at 15 nm Pd and 2 nm Pt, CO oxidation at 16 nm, 8 nm
and 1.4 nm gold and NO reduction with NH3 at 2 nm Rh particles were performed, indicating that the novel catalysts might in principle be applicable in technical processes
if the experimental conditions like form and temperature would be optimized.
Dedicated to Professor Dieter Fenske on the occassion of his 65th birthday. 相似文献
162.
Yoann Coquerel 《Journal of organometallic chemistry》2007,692(22):4805-4808
The palladium hydride-iminium complex generated from Pd/C and triethylamine catalyses the isomerisation of allylic alcohols into carbonyl compounds, and Pd/C catalyses the conjugate reduction of activated double bonds using triethylamine as the source of the two newly incorporated hydrogen atoms via the same complex. 相似文献
163.
Laurence E. Strong Thomas G. Copeland Margaret Darragh Carter Van Waes 《Journal of solution chemistry》1980,9(2):109-128
Conductivities of aqueous solutions ofortho-, meta-, andpara-toluic acids have been measured for the concentration range 0.1–2 millimolar and at 5° intervals from 5 to 100°C. At each temperature pK
a(m) andA
0 have been calculated using the paired ion model recently described by Fuoss. Thermodynamic parameters have been calculated for the ionization of each acid, and Walden products for the anions. Results are discussed in terms of contributions to acidity by enthalpy and entropy changes as well as by hydration of the various solute species. 相似文献
164.
A practical and efficient stereoselective synthesis of the side chain of neomarinone is reported. The synthesis was achieved in six steps (41% overall yield) from 2-methyl-2-cyclohexenone. The key step is a novel stereoselective 1,4-conjugate addition/enolate alkylation by an epoxide-opening reaction. 相似文献
165.
Dr. Pradip Ghosh Sander de Vos Dr. Martin Lutz Dr. Frederic Gloaguen Prof. Dr. Philippe Schollhammer Dr. Marc-Etienne Moret Prof. Dr. Robertus J. M. Klein Gebbink 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(55):12560-12569
Homogeneous electrocatalytic proton reduction is reported using cobalt complex [ 1 ](BF4)2. This complex comprises two bis(1-methyl-4,5-diphenyl-1H-imidazol-2-yl)methane (HBMIM ) ligands that contain an acidic methylene moiety in their backbone. Upon reduction of [ 1 ](BF4)2 by either electrochemical or chemical means, one of its HBMIM ligands undergoes deprotonation under the formation of dihydrogen. Addition of a mild proton source (acetic acid) to deprotonated complex [ 2 ](BF4) regenerates protonated complex [ 1 ](BF4)2. In presence of acetic acid in acetonitrile solvent [ 1 ](BF4)2 shows electrocatalytic proton reduction with a kobs of ≈200 s−1 at an overpotential of 590 mV. Mechanistic investigations supported by DFT (BP86) suggest that dihydrogen formation takes place in an intramolecular fashion through the participation of a methylene C−H bond of the HBMIM ligand and a CoII−H bond through formal heterolytic splitting of the latter. These findings are of interest to the development of responsive ligands for molecular (base)metal (electro)catalysis. 相似文献
166.
Let G be a simple graph with adjacency matrix A(G) and (G,x) the permanental polynomial of G. Let G × H denotes the Cartesian product of graphs G and H. Inspired by Kleins idea to compute the permanent of some matrices (Mol. Phy. 31 (3) (1976) 811–823), in this paper in terms of some orientation of graphs we study the permanental polynomial of a type of graphs. Here are some of our main results.1.If G is a bipartite graph containing no subgraph which is an even subdivision of K
2,3, then G has an orientation G
e such that (G,x) = det (xI-A(G
e
)), where A(G
e
) denotes the skew adjacency matrix of G
e.2.Let G be a 2-connected outerplanar bipartite graph with n vertices. Then there exists a 2-connected outerplanar bipartite graph
with 2n+2 vertices such that (G,x) is a factor of
.3.Let T be an arbitrary tree with n vertices. Then
, where
1
,
2
, ...,
n are the eigenvalues of T. 相似文献
167.
168.
169.
The reducing system NiCl2·2H2O—Li—arenecat (cat is catalyst) was proposed for use to reduce a wide range of organic compounds, including alkenes, alkynes, carbonyl compounds, imines, halogenated derivatives, sulfonates, aromatic compounds, hydrazines, azo and azoxy compounds, N-oxides, and nitrones. The degree of reduction can be controlled for some substrates. Deuterium can be incorporated in the reaction products using nickel chloride deuteriohydrate. Nitrones, N-alkoxyamides, and acyl azides are also reduced with the Li—arenecat system containing no nickel salt. 相似文献
170.
S. N. Dmitrieva N. I. Sidorenko A. I. Vedernikov L. G. Kuz’mina J. A. K. Howard T. M. Buslaeva S. P. Gromov 《Russian Chemical Bulletin》2007,56(5):993-1002
The condensation reaction of 1,2-bis(2-haloethoxy)-4-nitrobenzenes with acyclic α,ω-(oxa)alkanedithiols in the presence of
alkali metal carbonates produced a series of nitrobenzodithiacrown ethers with macrocycles of different size. The structures
of three ethers were established by X-ray diffraction. A new method was developed for the synthesis of nitrobenzomonothia-15-crown-5
ether. Nitro derivatives of benzodithiacrown ethers were tested as reagents for extraction of palladium(II), platinum(IV), and rhodium(III) from hydrochloric acid solutions. Extraction of PdII salts was found to be highly selective compared to that of PtIV and RhIII salts. Benzodithia-15-crown-5 ether is the most efficient extractant for palladium(II). Reduction of nitrobenzothiacrown ethers with hydrazine hydrate in the presence of a platinum catalyst afforded their amino
derivatives.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 958–966, May, 2007. 相似文献