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991.
Four novel transitional metal complexes with 3-(4-pyridly)-4-phenyl-5-sulfhydryl- 1,2,4- triazole (HL1) and 3-(3-pyridly)-4-phenyl-5-sulfhydryl-l,2,4-triazole (HLz) were synthesized and characterized by elemental analysis, IR and X-ray diffraction. Complexes 1, 3 and 4 have two-dimensional (2-D) neutral rhombohedral grid with a (4, 4) topology. In 1, 3 and 4, all the metal ions are six-coordinated to four nitrogen atoms of four distinct ligands and two O atoms from water molecules. Complex 2 has tetranuclear CuaCI4 units which are interconnected by four desulfuri- zation ligands (L1-S) via Cu-N bonds to form a 2-D layer with (4,4) topology. 相似文献
992.
A new sandwiched polyoxometalate [HK11Cd4Cl2(PW9034)2]·18H2O (1), incor- porating a unique hybrid tetranuclear cadmium cluster (abbreviated to {Cd4}) with two trivacant polyanions [B-α-PW9O34]9-, has been hydrothermally synthesized and structurally characterized by elemental analyses, IR spectroscopy, UV-vis, and single-crystal X-ray diffraction analysis. Crystal data for 1: monoclinic, space group C2/c, a = 19.2997(4), b = 13.8014(3), c = 31.9819(8) A, β = 102.764(2)°, V= 8308.3(3) A3, Z = 4, P2O86Cl2K11Cd4W18H37, Mr = 5735.13, Dc = 4.584 mg-mm-3, F(000) = 10084, μ = 26.579 mm-1, the final R = 0.0378 and wR = 0.0989 for 6558 observed reflections (I〉 2σ(I)). X-ray crystallographic study shows that the molecular structure of 1 contains four cadmium atoms. Two CdO6 distorted octahedra and two CdOsC1 distorted octahedra combine with each other in turn via edge-sharing, resulting in a regular rhomb-like cluster sandwiched between two {B-a-PW9034} units. Further, the sandwich-type polyoxoanions were connected by K+ ions to form a complicated 3-D open-framework through connecting with each terminal O atom of the [Cd4C12(PW9O34)2]12- polyoxoanions. In addition, compound 1 exhibits photoluminescence property at room temperature and the band gap can be assessed at 3.25 eV. 相似文献
993.
994.
995.
On the ground of the ferrohydrodynamic model proposed by Shliomis and , the present study investigates the influences of fluid inertia forces on the ferrofluid squeeze film between a sphere and a plate in the presence of external magnetic fields. According to the results, the effects of fluid inertia forces enhance the load capacity and prolong the approaching time for the ferrofluid sphere–plate system. Further numerical results for the load capacity are also provided in a table for engineering applications. 相似文献
996.
Jennifer E. Mihalick William P. Griffiths III James E. Muten Travis A. Olson John B. Hein 《Journal of solution chemistry》1999,28(8):1019-1030
Solution calorimetry was used to determine enthalpies and stability constants for binding of lead(II) or cadmium(II) by galacturonic acid and several monosaccharides in aqueous solution. New values for enthalpies of solution in water are reported for galacturonic acid and maltose monohydrate. The interaction of water solvent with the reactants is the largest factor in the binding process. 相似文献
997.
F. Gordon A. Reference to Stone 《Journal of fluorine chemistry》1999,100(1-2):227-234
Early studies on organo-transition metal complexes with fluorocarbon ligands are reviewed in a historical context in relation to the renaissance of organometallic chemistry which followed the discovery of ferrocene. 相似文献
998.
Micelles,microemulsions.vesicles,etc.,areorganicmicroheterogeneousmedia.Useofthesemediainanalyticalreactionsfordevelopingnewkinetic-baseddeterminationsorimprovingpreviouslyestablishedkineticmethodshasbeenreported"2.Inrecentyears,amixedmicellarmediumc... 相似文献
999.
Effendy Ronald R. Fenton Leonard F. Lindoy Jason R. Price Brian W. Skelton Tania Strixner Gang Wei Allan H. White 《Journal of inclusion phenomena and macrocyclic chemistry》2001,41(1-4):185-191
As part of an ongoing investigation of the factors influencing metal ionrecognition, we have investigated structure/function relationships involvingthe metal-ion binding by three new N-benzyl-substituted, 15- and 16-membered,macrocyclic ligands incorporating N2O 3- and N 3O 3-donor sets (withthe N 3O 3-system consisting of a N 2O 3-macrocyclic ring with an attachedCH 2CH 2NCH 2C 6H 5 pendant arm). Selected solid complexes of thelatter ligand were isolated and the X-ray structures of individual Ni(II) and Ag(I) complexeswere obtained.Where solubility permitted, potentiometric titration studies in 95% methanolwere employed to investigate the binding affinities of all three ligand derivativestowards Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Ag(I) and Pb(II). The 15-memberedN 2O 3-ring was found to be selective for Ag(I) over the other six metalsinvestigated, including Cu(II). However, the presence of a further nitrogen donorin the form of the pendant benzylamine functionality in the N 3O 3-donorsystem results in an increase in its binding affinity for Ag(I) but an even greaterincrease occurs for Cu(II). As a consequence, the latter ion is now more stronglybound than Ag(I). The factors influencing these respective selectivities are discussed. 相似文献
1000.
1INTRODUCTIONThecalculationsinthefirstpapershowedthatreal andcomplex orbitalmethodsderivedfromamodelofelectronic intersupplem... 相似文献