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31.
Metal-organic frameworks with exceptionally high capacity for storage of carbon dioxide at room temperature 总被引:4,自引:0,他引:4
Metal-organic frameworks (MOFs) show high CO2 storage capacity at room temperature. Gravimetric CO2 isotherms for MOF-2, MOF-505, Cu3(BTC)2, MOF-74, IRMOFs-11, -3, -6, and -1, and MOF-177 are reported up to 42 bar. Type I isotherms are found in all cases except for MOFs based on Zn4O(O2C)6 clusters, which reveal a sigmoidal isotherm (having a step). The various pressures of the isotherm steps correlate with increasing pore size, which indicates potential for gas separations. The amine functionality of the IRMOF-3 pore shows evidence of relatively increased affinity for CO2. Capacities qualitatively scale with surface area and range from 3.2 mmol/g for MOF-2 to 33.5 mmol/g (320 cm3(STP)/cm3, 147 wt %) for MOF-177, the highest CO2 capacity of any porous material reported. 相似文献
32.
The redox behaviour of adsorbed species of 2,4,6-tri(2-pyridyl)-1,3-5-triazine (TPTZ) at the surface of a mercury electrode was examined using cycling voltammetry. Based on the adsorption and accumulation of TPTZ at the charged mercury surface cathodic adsorptive stripping voltammetry (CSV) is applied for the trace determination of TPTZ using a differential pulse (DP) technique. Experimental and operational parameters for the quantitative analysis of TPTZ are optimized and the detection limit was found to be 3×10–9 mol/l. The effect of some interferences, e.g. organic compounds, cations and anions, are investigated. 相似文献
33.
A. J. Abu El-Haija K. A. Al-Saleh N. A. Halim J. M. Khalifeh N. S. Saleh 《Journal of Radioanalytical and Nuclear Chemistry》1988,120(2):387-392
The ion-beam mixing of Sn thin film evaporated on silicon has been investigated by continuously measuring the electrical resistivity of the sample during irradiation by Kr ions. The resistivity results exhibit a tendency toward a saturation process and allow the determination of the critical dose corresponding to the total mixing condition. The variation of the volume fraction of intermixed atoms as a function of the ion dose has been deduced and compared with a semiempirical formula to explain the observed mixing kinetics. A linear dependence of the volume fraction of the intermixed atoms on the fluence is observed, which is a signature of recoil type mixing. 相似文献
34.
35.
[reaction: see text] Chelation between gamma-hydroxybutynenitrile and Grignard reagents triggers a particularly facile anionic conjugate addition reaction. Structurally diverse Grignard reagents add with equal efficiency, providing an intermediate anion that stereoselectively alkylates benzaldehyde in an overall addition-alkylation reaction. 相似文献
36.
The method is based on the highly sensitive reaction between cobalt and 4-(5-bromo-2-pyridylazo)-l,3-diaminobenzene. The cationic complex in slightly acidic solution is quantitatively extracted into chloroform as an ion pair with anthraquinone sulfonate; interfering ions are retained in the aqueous phase by selected masking agents. The cobalt complex is then rapidly back-extracted into 2.4 M HCl and measured at 573 nm (? = 1.16 × 105 l mol-1 cm-1). 相似文献
37.
El-Said Asma I. Zidan Amna S. A. El-Meligy Mahmoud S. Aly Aref A. M. Mohammed Omar F. 《Transition Metal Chemistry》2001,26(1-2):13-19
Complexes of 1,10-o-phenanthroline (o-phen)-NiII and CuII with dithiocarbamates derived from -amino acids (glycine, phenylalanine, alanine, methionine and tryptophan) were synthesized and characterized by chemical analysis, spectral and thermal studies and by biological screening; the complexes are non-electrolytes. The empirical formula are [Ni(o-phen)2(aadtc)] and [Cu2(o-phen)2(phaladtc)(H2O)2Br2] where, aadtc = glycinyl-, phenylalaninyl-, alaninyl-, methioninyl- and tryptophanyldithiocarbamate and phaladtc = phenylalaninyldithiocarbamate. The structure of these complexes is probably octahedral. Molecular association through hydrogen bonding between the —NH and the carboxylate groups is proposed for the NiII complexes. The CuII complex is dimeric with the phenylalaninyldithiocarbamate acting as a bridge. 相似文献
38.
A novel homotrifunctional conjugation reagent, 1,3,5-tris-(N-maleimidomethyl)benzene has been synthesized in high yield with minimum purification. The reactivity of this compound was examined by using l-cysteine as a nucleophile. 相似文献
39.
Hamed M. Abu El-Nader 《Transition Metal Chemistry》1995,20(3):316-319
Summary The kinetics of the thermal decomposition of thetris-oxalactocobaltate(III) complex has been investigated in the presence of EtOH and (CH2OH)2 spectrophotometrically in the 50–70 ± 0.1 ° C range. The rate of the reaction decreases upon the addition of either of the alcohols to the reaction medium, whereas the activation energy increases. The thermodynamic parameters were calculated and are discussed in terms of the solvation effects. The influence of the dielectric constants of the solvent mixtures on the rate has been studied. A free radical mechanism is proposed and discussed. 相似文献
40.
Gaber M. Abu El-Reash 《Transition Metal Chemistry》1993,18(5):493-496
Summary The synthesis and characterization of CrIII, MnII, FeIII, CoII, NiII, CuII, ZnII, CdII and UO
inf2
sup2+
complexes of N-isonicotinamido-N-benzoylthiocarbamide (H2IBTC) are reported. I.r. spectral data show that the ligand behaves in a bidentate, tridentate and/or tetradentate manner. Different stereochemistries are proposed for CrIII, MnII, FeIII, CoII, NiII and CuII complexes on the basis of spectral and magnetic studies. The i.r. data indicate that the carbonyl oxygen of the benzoyl moiety is the backbone of chelation in most complexes. 相似文献