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111.
Tomasz Smolinski Danuta Wawszczak Andrzej Deptula Wieslawa Lada Tadeusz Olczak Marcin Rogowski Marta Pyszynska Andrzej Grzegorz Chmielewski 《Journal of Radioanalytical and Nuclear Chemistry》2017,313(1):69-77
A micro-cloud point extraction method was discussed for preconcentration and spectrophotometric quantification of U(VI). The method depends on complex formation between U(VI) and 2-(4-sulphophenyloazo)-1,8-dihydroxy-3,6-naphtalenedisulphonic acid (SPADNS) at pH 7.0 and subsequent extraction of the complex in a mixed surfactant medium (cethyltrimethyl ammonium bromide and Triton X-114). The separation was carried out in the presence of 1% Na2SO4 at room temperature. The calibration curve was linear up to 3000 µg L?1. The enrichment factor, detection limit and precision were 16.0, 1.05 µg L?1, and 2.3%, respectively. The method was employed for the determination of U(VI) in real samples with different matrices. 相似文献
112.
McIntosh JA Robertson CR Agarwal V Nair SK Bulaj GW Schmidt EW 《Journal of the American Chemical Society》2010,132(44):15499-15501
A protease from ribosomal peptide biosynthesis macrocyclizes diverse substrates, including those resembling nonribosomal peptide and hybrid polyketide-peptide products. The proposed mechanism is analogous to thioesterase-catalyzed chemistry, but the substrates are amide bonds rather than thioesters. 相似文献
113.
A series of vanadium(V) complexes with unsymmetrical tridentate Schiff base ligands, obtained by the single condensation of R(−)-1,2-diaminopropane with salicylaldehyde and its derivatives, 2-hydroxy-1-naphthaldehyde, 2-hydroxyacetophenone, 1-hydroxy-2-acetonaphthone and 2-hydroxybenzophenone, were prepared. The complexes were characterized by elemental analysis and by their IR, CD, UV–Vis, 1D (1H, 51V) and 2D (COSY, NOESY, gHSQC) NMR spectra. Crystal structures of the mononuclear complex {R(−)-2-amino-1-N-[(2′-oxido-κO-4′,6′-dimethoxyphenyl)methylene]aminopropane-κ2N}dioxidovanadium(V), VO2(C12H17N2O3), 4, and of the dinuclear complex, di-μ-oxido-bis({R(−)-2-[1-(2-aminopropylimino)ethyl]-4-methylphenolato-κ3N,N′,O}oxidovanadium(V)), V2O4(C11H15N2O)2, 5, have been obtained by X-ray diffraction studies. The structure of 4 was revealed to be a distorted trigonal–bipyramidal coordination geometry, rarely encountered in VO2(tridentate Schiff base) complexes. Complexes 2 and 3 have the ability to catalyze the oxidation of prochiral sulfide substrates PhSR (R = Me, Bz) utilizing hydrogen peroxide or cumene hydroperoxide (CHPO) as the oxidant. 相似文献
114.
Elżbieta Lipiec Grzegorz Siara Katarzyna Bierla Laurent Ouerdane Joanna Szpunar 《Analytical and bioanalytical chemistry》2010,397(2):731-741
A method for the simultaneous determination of selenomethionine (SeMet), selenocysteine (SeCys), and selenite [Se(IV)] in
chicken eggs was developed. A sample preparation protocol including defatting, protein denaturation, and carbamidomethylation
was optimized in order to achieve complete protein digestion and to avoid SeCys losses. Quantification was carried out by
reversed-phase HPLC–inductively coupled plasma mass spectrometry (ICP MS) after quantitative isolation of the selenium-containing
fraction by size-exclusion liquid chromatography. The detection limits were 0.06, 0.003, and 0.01 μg g−1 (dry weight) for SeCys, Se(IV) and SeMet, respectively, and the precision was 5–10%. The end products of carbamidomethylation
of the different selenium species were identified for the first time by electrospray QTOF MS after custom-designed 2D HPLC
purification. Differences in selenium speciation in egg yolk and white were highlighted, the yolk containing more SeCys and
the white more SeMet. An insight into selenium bioaccessibility in eggs was obtained by digestion with simulated gastric and
gastrointestinal juices and size-exclusion HPLC-ICP MS. 相似文献
115.
Jaworska M Hrynczyszyn PB Wełniak M Wojtczak A Nowicka K Krasiński G Kassassir H Ciesielski W Potrzebowski MJ 《The journal of physical chemistry. A》2010,114(47):12522-12530
Two analogous Schiff bases, (S,E)-2-((1-hydroxy-3-methyl-1,1-diphenylbutan-2-ylimino)methyl)phenol (1) and (S,Z)-2-hydroxy-6-((1-hydroxy-3-methyl-1,1-diphenylbutan-2-ylamino)methylene)cyclohexa-2,4-dienone (2), exist in the solid state as phenol-imine and keto-amine tautomers, respectively. Their crystal structures were solved using the X-ray diffraction method. Sample 1 forms orthorhombic crystals of space group P2(1)2(1)2(1), while 2 forms monoclinic crystals of space group P2(1). In each sample, one molecule is in the asymmetric unit of the crystal structure. One-dimensional and two-dimensional solid state NMR techniques were used for structure assignment and for inspection of the (13)C and (15)N δ(ii) of the chemical shift tensor (CST) values. NMR study indicates that the span (Ω = δ(11)-δ(33)) and the skew (κ = 3(δ(22)-δ(iso)/Ω) are extremely sensitive to change in the tautomeric form of the Schiff bases. Theoretical calculations of NMR shielding parameters for 1 and 2 and a model compound with reduced aliphatic residue were performed using the GIAO method with B3LYP functional and 6-311++g(d,p) basis sets. From comparative analysis of the experimental and theoretical parameters, it was concluded that the position of hydrogen in the intramolecular bridge has tremendous influence on (13)C and (15)N CST parameters. Inspection of Ω and κ parameters allowed for the establishment of the nature of the hydrogen bonding and the assignment of the equilibrium proton position in the intramolecular bridges in the solid state. 相似文献
116.
Magdalena Śliwka-Kaszyńska Grzegorz Gorczyca Marek Ślebioda 《Journal of chromatography. A》2010,1217(3):329-336
Twelve calix[4]arene stationary phases in 1,3-alternate conformation, synthesized in the authors’ laboratory, were characterized in terms of their surface coverage, hydrophobic selectivity, aromatic selectivity, shape selectivity, hydrogen bonding capacity and ion-exchange capacity. The set of tests commonly used for evaluation of commercially available stationary phases was applied to assess fundamental chromatographic properties of the calixarene phases. The new calixarene phases were compared to each other, to Caltrex and LiChrosorb C-18 columns. Principal component analysis has been used to provide comparison between 1,3-alternate calix[4]arene phases and commercially available phenyl, fluorophenyl and fluoroalkyl columns. 相似文献
117.
Grzegorz Dutkiewicz B. P. Siddaraju H. S. Yathirajan B. Narayana Maciej Kubicki 《Journal of chemical crystallography》2010,40(11):970-974
Abstract
The title compound, C22H28F3N3OS2+ × 2(C6H2N3O7 −) × (CH3)2SO—the picrate salt of the potent antipsychotic drug, fluphenazine—crystallizes in the triclinic P-1 space group with unit cell parameters a = 10.6333(12) ?, b = 11.9696(12) ?, c = 17.7036(15) ?, α = 103.265(9)°, β = 98.414(9)°, γ = 102.702(10)°. The ionic fragments: the fluphenazinium dictation, and two picrate anions, are joined by means of strong N–H···O and weak C–H···O hydrogen bonds into the chains of alternating cations and anions, expanding along [010] direction. Within the chain, the picrates interact by means of short π···π interactions: the mean distance between the planes is 3.366 ?; additional interaction of the same type between one of the picrates and the phenyl ring of the phenothiazine ring system additionally strengthen the pattern. The phenothiazine ring exists in a typical, “butterfly-like” conformation, with two terminal rings planar and the central ring in a slightly flattened boat form. This conformation results in the dihedral angle between the terminal rings of 41.76(5)°. The aliphatic chain which substitutes phenothiazine at N-position is not in an extended conformation, the torsion angles along this chain are 75.95(14)° and −163.96(10)°. The structure contains also the solvent—dimethylsulphoxide molecules, which are connected with the cation–anion structure by means of strong O–H···O hydrogen bonds. 相似文献118.
Dominika Teklinska Kinga Kosciewicz Kacper Grodecki Mateusz Tokarczyk Grzegorz Kowalski Wlodzimierz Strupinski Andrzej Olszyna Jacek Baranowski 《Central European Journal of Physics》2011,9(2):446-453
Polytype instability of SiC epitaxial films was the main focus of attention in the experiment performed since this factor
has a decisive influence on graphene growth, which was the second stage of the experiment. Layers deposited in various initial
C/Si ratios were analyzed. 相似文献
119.
Okunev VD Samoilenko ZA Szewczyk A Szymczak R Szymczak H Lewandowski SJ Aleshkevych P Wi?ckowski J Khmelevskaya VS Antoshina IA 《J Phys Condens Matter》2011,23(41):415702
We have reinforced local superconductivity in ferromagnetic Fe(67)Cr(18)B(15) metallic glasses by ion irradiation. Superconductivity in this medium appears due to the presence of large-scale layered clusters of metallic Fe-Cr phase, 150-230 ? in size, with a ferromagnetic (or superparamagnetic) Fe-rich core and nonmagnetic Cr-rich superconducting shell. Here we show that due to the intensification of concentration phase separation in the Fe-Cr clusters under ion (Ar(+)) irradiation, the volume of the superconducting phase increases from the initial 0.4-0.5% up to 7-8%. After irradiation, the resistivity jump Δρ/ρ in the temperature range T=3.1-3.6 K increases ~14 times, reaching 19%, as compared to 1.36% for the initial sample. In the interval of T=3.1-3.6 K, the rate of resistance change reaches 79% K(-1) for the irradiated sample instead of 3.6% K(-1) for the initial sample. In the same temperature interval, the rate of magnetoresistance change increases from 3% K(-1) for the initial sample up to 70% K(-1) after irradiation. 相似文献
120.