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991.
Pure and Mn-doped NaTaO3 nanoparticles were synthesized by a simple hydro- thermal method. XRD and XPS results suggested that manganese ions were successfully doped into the NaTaO3 crystalline in Mn2+ state. UV-vis diffuse reflectance spectra revealed the obvious red-shift in the series of manganese doped NaTaO3 nanoparticles, resulting in a decrease in the band gap of NaTaO3 with the increase of Mn2+ doping concentration. The photo-degradation experiment indicated that manganese doped NaTaO3 showed good photocatalytic performance and methylene blue(MB) degradation is improved with lower doping concentration of manganese ions under visible light. The simulation of energy band structure by density functional theory unfolded that the substitution of Ta5+ ions by Mn2+ ions resulted in an intermediate band(IB) below the bottom of the conduction band(CB), which was mainly attributed to the state of Mn 3d. 相似文献
992.
A new tetranuclear cluster [Co4(bm)6Cl2]·(H2O)2·(CH3OH)(1, Hbm is(1H-benzimidazol-2-yl)-methanol) has been synthesized by solvothermal method and structurally determined by IR, elemental analysis, and single-crystal X-ray diffraction. Complex 1 belongs to monoclinic space group P21/n with a = 21.1713(5), b = 12.7948(3), c = 24.0195(9) , β = 95.309(3)°, V = 6478.6(3) 3, Z = 4, F(000) = 2568, Dc = 1.289 g·cm–3, Mr = 1257.63, μ = 9.096 mm–1, S = 1.000, the final R = 0.0861 and wR = 0.2552 for 4956 observed reflections with I 2σ(I). Two connected face-sharing cubes are observed in the framework of 1, each with one vertex missing. Complex 1 forms a 2-D network through N–H···O hydrogen bonds. The apparent holes can be observed. 相似文献
993.
Two macrocyclic zinc(II) complexes {[ZnL(VO3)2]·0.33H2O}n(1) and [ZnL(H2O)2][Ni(CN)4](2)(L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane) have been obtained from the reactions of [ZnL](ClO4)2 with NH4VO3 and K2[Ni(CN)4], respectively, and structurally characterized by elemental analysis, IR, XRPD, TG and X-ray diffraction. Single-crystal X-ray diffraction analyses indicated that the Zn(II) atom lies on an inversion center and is octahedrally coordinated by four nitrogen atoms of the tetradentate macrocyclic ligand in the equatorial plane and two oxygen atoms of [VO4] tetrahedra in the axial positions in 1, and two oxygen atoms of two water molecules in 2. Complex 1 shows a three-dimensional structure, which is constructed by the links of [VO3]nn- chains with [ZnL]2+, forming one-dimensional channels occupied by guest water molecules. The monomers of [ZnL(H2O)2]2+ and [Ni(CN)4]2- are connected through the intermolecular hydrogen bonds to form a two-dimensional sheet in complex 2. 相似文献
994.
The complex [Cd(bbb)Cl2]·DMF·H2O, where bbb is 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole, was synthesized and characterized by X-ray single-crystal structure analyses. For the complex: C24H25Cl2CdN5O2, Mr = 598.77, crystal system, triclinic, space group P1, a = 9.9878(12), b = 10.0008(12), c = 13.2217(15) , α = 80.674(2), β = 72.158(2), γ = 86.776(2)°, V = 1240.5(3) 3, Z = 2, Dc = 1.598 g/cm3, λ = 0.71073, μ(MoKα) = 1.127 mm–1, F(000) = 600, S = 1.04, R = 0.0905 and wR = 0.3088 for 4805 observed reflections with I 2σ(I). It is a neutral complex. The distorted tetrahedral geometry of cadmium ion is coordinated by two nitrogen atoms of ligand and two chloride ions. The complex emits blue green luminescence with emission peaks at 480 nm in DMF solution. 相似文献
995.
A new 3D heterometallic coordination polymer, namely [K2Pr2(C2O4)4·H2O]n(1), has been successfully synthesized under hydrothermal conditions. X-ray single-crystal diffraction determination reveals that 1 crystallizes in monoclinic system, space group P21/n with a = 12.060(4), b = 8.493(3), c = 15.776(5)(A), β = 93.235(3)°, V = 1613.4(9) 3, Z = 4, Mr = 730.12, Dc = 3.006 Mg/m3, μ = 6.581 mm-1, F(000) = 1368, the final R = 0.0283 and w R = 0.0866 for 2939 observed reflections with I 2σ(I). Complex 1 features an unusual 3D heterometallic coordination framework, in which oxalates exhibit three different coordination behaviours. Moreover, powder X-ray diffraction and thermal properties for 1 have also been investigated. 相似文献
996.
One novel organically templated zincophophate(C5N2H14)·[Zn3(OH2)(PO4)2(HPO4)] has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction together with elemental analysis, infrared spectroscopy, thermogravimetric analysis, and powder X-ray diffraction. The title compound crystallizes in the monoclinic space group P21/n, with a = 9.7904(11), b = 14.0287(14), c = 11.8651(13) , β = 104.690(3), V = 1576.4(3) 3, Z = 4, T = 296(2) K, Mr = 601.31 and Dc = 2.533 g/cm3. The compound consists of a macroanionic [Zn3(OH2)(PO4)2(HPO4)]2- framework and(C5N2H14)2+ cations, and its structure is built up from ZnO3(OH2), ZnO4, HPO4 and PO4 tetrahedral units that result in 4, 8 and 10-ring channels. 相似文献
997.
A new 2D barium-organic framework, [Ba2(Hbidc)2]n(1, Hbidc = 1H-benzimidazole-5,6-dicarboxylate), has been solvothermally synthesized and structurally characterized by elemental analysis, IR spectroscopy, TGA, powder X-ray diffraction, and single-crystal X-ray diffraction. The crystal belongs to the triclinic system, space group P1 with a = 6.8785(14), b = 9.4558(19), c = 14.641(3) , α = 86.22(3), β = 82.27(3), γ = 88.40(3)°, V = 941.4(3) 3, Z = 2, Mr = 682.96, Dc = 2.409 g/cm3, μ(MoKα) = 4.217 mm-1, F(000) = 640, the final R = 0.0587 and wR = 0.1619 for 3030 observed reflections with I 2σ(I). Structural determination reveals that 1 exhibits an interesting 2D layer structure constructed by carboxylate groups of Hbidc ligands and shows good thermal stability(up to 400 ℃). Solid-state 1 emits intense indigotin photoluminescence with fluorescence lifetime of 62.13(408 nm) at room temperature. The H3bidc ligand and its barium complex have been screened for antibacterial activity against several bacteria strains, and the results are compared with the activity of penicillin. 相似文献
998.
pH-sensitive wettability of polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) self assembled films, exhibiting superoleophobicity under water and hydrophilicity at low pH value, and oleophobicity under water and hydrophobicity at neutral condition, has been realized. The wettability properties resulted from the surface topological and chemical transition, which were confirmed by in situ AFM measurements under water at different pH. At low pH, P4VP chains, which were confined in the hexagonal-packed nanodomains, got protonated into a swollen state, while at high pH, P4VP chains were deprotonated into a collapsed state. The reversible protonation/deprotonation procedure on the molecular scale leads to surface topological and chemical transition, thereby pH-sensitive wettability. 相似文献
999.
Polyamide I1 (PAll) and its nanocomposites with different organoclay loadings were prepared by melt-compounding and subsequent pelletizing. The crystal phase transitions of PAl 1 and its clay nanocomposites were investigated by variable-temperature X-ray diffraction. It was found that the Brill transition of the nanocomposite was 20 K higher than that of the neat PAl 1 for both heating and cooling processes. The PAl 1 d-spacings of the nanocomposites were observed to be smaller than those of the neat PAl 1 for melt crystallization. The constraints imposed by the addition of layered clay, restricting the thermal expansion of the polymer chains, are probably responsible for such a reduction of the d-spacing. 相似文献
1000.
A low operating pressure nanofiltration membrane is prepared by interfacial polymerization between m-phenylenediamine(MPDA) and trimesoyl chloride(TMC) using PVC hollow fiber membrane as supporting.A series of PVC nanofiltration membranes with different molecular weight cutoff(MWCO) can be obtained by controlling preparation conditions.Chemical and morphological characterization of the membrane surface was carried out by FTIR-ATR and SEM.MWCO was characterized by filtration experiments.The preparation conditions were investigated in detail.At the optimized conditions(40 min air-dried time,aqueous phase containing 0.5% MPDA,0.05% SDS and 0.6% acid absorbent,oil phase containing 0.3% TMC,and 1 min reaction time),under 0.3 MPa,water flux of the gained nanofiltration membrane reaches 17.8 L/m2·h,and the rejection rates of methyl orange and MgSO4 are more than 90% and 60%,respectively. 相似文献