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141.
Ming Z. Gao 《Tetrahedron letters》2004,45(29):5649-5652
The novel structures of sulfur-containing chiral bis(oxazoline) compounds which have been synthesized have been determined by X-ray crystal diffraction analyses. A high enantioselectivity (ee >99%) in the asymmetric cyclopropanation of diphenylethene with diazoester using the bis(oxazoline)-Ru(II) catalyst was obtained. 相似文献
142.
Double C-C bond cleavage of a cyclopentadienyl ligand proceeded to titanacyclopentadienes when 2 equiv of nitriles were added and the resulting two-carbon unit and three-carbon unit were converted into a benzene derivative and a pyridine derivative, respectively, in one-pot. 相似文献
143.
Hongye Tian Jun Shao Rong He Feng Gao Daxiang Cui Hongchen Gu 《Frontiers of Chemistry in China》2006,1(4):474-478
Quantum dots (QDs) were prepared in an organic system through a simple and low-cost wet chemistry method. Polymer beads with
a diameter of 60–70 nm and specific functional groups were synthesized by a particular seeded emulsion polymerization technique.
QDs were embedded in the polymer beads with the specific functional groups through dissolving and swelling method, which provided
the condition for the conjunction of biomolecules and QDs as fluorescent probes. The prepared composites were characterized
with UV-Vis, PL, TEM, FTIR, CLSM and conductance titration etc. The results show that QDs are successfully embedded in polymer
beads, which breaks the limitation that the conjunction of biomolecules and QDs can be achieved only for those synthesized
in aqueous system.
__________
Translated from Journal of Shanghai Jiaotong University, 2005, 39(1) (in Chinese) 相似文献
144.
Chen T Barton SC Binyamin G Gao Z Zhang Y Kim HH Heller A 《Journal of the American Chemical Society》2001,123(35):8630-8631
145.
Synchrotron radiation X-ray fluorescence (SRXRF) spectroscopy is an advanced method of quantitative multielemental analysis with space resolution of several microm and sensitivities in the microg g(-1) range. It can be used for keeping track of trace elements after an electrophoretic separation of biological samples. In this paper, proteins in human liver cytosol were separated with gel filtration chromatography and thin layer isoelectric focusing (IEF). The contents of metal ions in protein bands were determined by SRXRF. The results showed that in the molecular weight (MW) range of 10 approximately 25 kDa, there were at least 2 Zn-containing bands with isoelectric point (pI) of 5 approximately 6 and 6.2 approximately 7, respectively and about 11 Fe-containing proteins with pI of 4.4, 4.6, 4.8, 5.0, 5.2, 5.3, 5.5, 5.6, 6.6, 6.8, and 7.2, respectively, present in human liver cytosol. The Zn-containing band with pI of 5-6 is the dominant species of zinc in this MW range. In addition, the Cu-containing bands with pI of 5.0 and below 4.8 were also detected. It is demonstrated that the procedure could be widely used in further investigations of the chemical species of trace elements in biological samples. 相似文献
146.
Highly dispersed α-Fe_2O_3/NaY,NiO/NaY,and CuO/NaY catalyst systems were pre-pared by impregnation method.Dispersion thresholds of the transition metal oxides on NaY" zeolitewere determined by XRD phase analysis.The dispersion capacities of the transition metal oxides on NaYzeolite are much lower than that estimated on the basis of a closed packed monolayer in the micropores.The catalytic activity and selectivity of the highly dispersed oxide catalyst systems for ethylben-zene and cyclohexane dehydrogenation reactions were reported. 相似文献
147.
Potential alternative to petrochemical polymers, soy protein isolate (SPI), a plentily available, natural biopolymer is chemically
modified with thiourea at 2.5, 5, 7.5, 10, 15 and 20 mass/mass% for better processing of plastic as a raw material. From the
FTIR studies, it has been ascertained that there is no bonding reaction between SPI and thiourea and it acts as a modifier
only. Thermogravimetric analysis of the modified material has been followed using a computer analysis method, LOTUS package,
developed by us for assigning the degradation mechanism. A number of equations have been used to evaluate the kinetic parameters.
The mechanism of degradation of the biopolymer is explained on the basis of the kinetic analysis. 相似文献
148.
149.
Protocatechuic acid esters (= 3,4‐dihydroxybenzoates) scavenge ca. 5 equiv. of radical in alcoholic solvents, whereas they consume only 2 equiv. of radical in nonalcoholic solvents. While the high radical‐scavenging activity of protocatechuic acid esters in alcoholic solvents as compared to that in nonalcoholic solvents is due to a nucleophilic addition of an alcohol molecule at C(2) of an intermediate o‐quinone structure, thus regenerating a catechol (= benzene‐1,2‐diol) structure, it is still unclear why protocatechuic acid esters scavenge more than 4 equiv. of radical (C(2) refers to the protocatechuic acid numbering). Therefore, to elucidate the oxidation mechanism beyond the formation of the C(2) alcohol adduct, 3,4‐dihydroxy‐2‐methoxybenzoic acid methyl ester ( 4 ), the C(2) MeOH adduct, which is an oxidation product of methyl protocatechuate ( 1 ) in MeOH, was oxidized by the DPPH radical (= 2,2‐diphenyl‐1‐picrylhydrazyl) or o‐chloranil (= 3,4,5,6‐tetrachlorocyclohexa‐3,5‐diene‐1,2‐dione) in CD3OD/(D6)acetone 3 : 1). The oxidation mixtures were directly analyzed by NMR. Oxidation with both the DPPH radical and o‐chloranil produced a C(2),C(6) bis‐methanol adduct ( 7 ), which could scavenge additional 2 equiv. of radical. Calculations of LUMO electron densities of o‐quinones corroborated the regioselective nucleophilic addition of alcohol molecules with o‐quinones. Our results strongly suggest that the regeneration of a catechol structure via a nucleophilic addition of an alcohol molecule with a o‐quinone is a key reaction for the high radical‐scavenging activity of protocatechuic acid esters in alcoholic solvents. 相似文献
150.
A New Reaction-controlled Phase-transfer Catalyst System 总被引:1,自引:0,他引:1
MingQiangLI XiGaoJIAN GuiMeiWANG YanYU 《中国化学快报》2004,15(3):350-352
A new reaction-controlled phase-transfer catalyst system was designed and synthesized.In this system, heteropolytungstate [C7H7N(CH3)3]9PW9O34 was used for catalytic epoxidation of cyclohexene with H2O2 as the oxidant. The conversion of H2O2 was 100% and the yield of cyclohexene oxide was 87.1% based on cyclohexene. Infrared spectra showed that both fresh catalyst and the recovered catalyst do have completely same absorption peak, indicating the structure of catalyst is very stability and can be recycled. 相似文献