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21.
A new effective approach to the synthesis of a small library of 2-amino-5-arylidene-1,3-thiazol-4(5H)-ones was reported using solvent-free reaction conditions under microwave irradiation. In the first step, rhodanines were subjected to Knoevenagel condensation with aryl aldimines according to a facile one-pot protocol. Then the (5Z)-5-arylidene rhodanine derivatives were transformed directly into the corresponding 2-amino-1,3-thiazol-4(5H)-ones by sulfur/nitrogen displacement reaction under microwaves with retention of configuration and good overall yields. 相似文献
22.
J. Grenet J. M. Saiter C. Vautier J. Bayard 《Journal of Thermal Analysis and Calorimetry》1992,38(4):557-565
The effect of ageing temperature (belowT
g) on physical ageing of glassy PET has been investigated by differential scanning calorimetry. The position of the glass transition endotherm was found to be strongly dependent on the annealing conditions (time, annealing temperature). A single relaxation time model is proposed for the analysis of physical ageing.The variations of the equilibrium relaxation time iso with annealing temperature allow the determination of the parameters of the model. Finally, using these constants, one can determine the thermal past and foresee the thermal future of unknown samples which are of prime importance in processes using temperatures around the glass transition temperature.
Zusammenfassung Mittels DSC wurde der Einfluß der Alterungstemperatur (unterhalbT g) auf das physikalische Altern von glasartigen PET untersucht. Die Lage der Glasumwandlungsendothermen hängt stark von den Temperungsbedingungen (Dauer, Temperungstemperatur) ab. Es wird ein Relaxationszeitmodell für die Analyse physikalischen Alterns vorgeschlagen.Die Parameter dieses Modelles knnen aus der Änderung der Gleichgewichtsrelaxationszeit iso mit der Temperungstemperatur ermittelt werden. Unter Benutzung dieser Konstanten kann die thermische Vergangenheit unbekannter Proben bestimmt und die thermische Zukunft derselben vorhergesagt werden, was für Vorgänge bei Temperaturen um den Glasumwandlungspunkt von primärer Wichtigkeit ist.相似文献
23.
Determining PPARγ-ligand binding affinity using fluorescent assay with cis-parinaric acid as a probe
Gao Zhenting Luo Haibin Chen Lili Shen Jianhua CHEN Kaixian JIANG Hualiang SHEN Xu 《中国科学B辑(英文版)》2005,48(2)
Upon the study of small-molecules binding to proteins, the traditional methods for calculating dissociation constants (Kd and Ki) have shortcomings in dealing with the single binding site models. In this paper, two equations have been derived to solve this problem. These two equations are independent of the total concentration or initial degree of saturation of receptor and the activity of the competitive molecule. Through nonlinear fitting against these two equations, Kd value of a probe can be obtained by binding assay, and Ki value of a ligand can be obtained by competitive assay. Moreover, only the total concentrations of receptor([R]t), ligand([L]t) and probe([P]t) are required for the data fitting. In this work, Ki values of some typical ligands of PPARγ were successfully determined by use of our equations, among which the Ki value of PPARγ-LY171883 was reported for the first time. 相似文献
24.
A novel electroless deposition method for depositing highly uniform adhesive thin films of copper selenide (Cu3Se2) on silicon substrates from aqueous solutions is described. The deposition is carried out by two coupled galvanic reactions in a single deposition bath containing copper cations, hydrogen fluoride, and selenous acid: the galvanic deposition of copper on silicon and the subsequent galvanic reaction between the deposited copper with selenous acid in the deposition bath. The powder X-ray diffraction and scanning electron microscopy are used to characterize and examine the deposited films. 相似文献
25.
Xiao Hua WANG Han Zhi WANG Hui LIU Yuan KOU 《中国化学快报》2006,17(12):1531-1533
Recent years, crown ethers have been used in many fields, including phase transfer catalysis, chromatography stationary phase, ionselective electrode, and concentration of metal ions, etc1.. However, the toxicity of free crown ethers makes them unsuitable for industrial use2. Introduction of a crown ether as a functional group to functionalized ionic liquids has been reported3. These functionalized ionic liquids will combine the excellent properties of crown ether and ionic liquids without los… 相似文献
26.
With the combination of the the stoichiometric displacement model for retention (SDM-R) in reversed phase liquid chromatography (RPLC) and the stoichiometric displacement model for adsorption (SDM-A) in physical chemistry,the total number of moles of the re-solvated methanol of stationary phase side.nr,and that of solute side in the mobile phase,q,corresponding the one mole of the desorbing solute,were separately determined and referred as the characterization parameters of the contributions of the adsorption mechanism and partition mechanism to the solute retention,respectively.A chromatographic system of insulin,using mobile phase consisting of the pseudo-homologue of alcohols(methanol,ethanol and 2-propanol)-water and trifluoroacetic acid was employed.The maximum number of the methanol layers on the stationary phase surface was found to be 10.6,only 3 of which being valid in usual RPLC,traditionally referred as a volume process in partition mechanism.However,it still follows the SDM-R.Both of q and nr of insulin were found not to be zero,indicating that the retention mechanism of insulin is a mixed mode of partition mechanism and adsorption mechanism.When methanol is used as the organic modifier,the ratio of q/nr was 1.13,indicating the contribution to insulin retention due to partition mechanism being a bit greater than that due to adsorption mechanism.A linear relationship between q,or nr and the carbon number of the pseudo-homologue in the mobile phase was also found.As a methodology for investigating the retention mechanism retention and behavior of biopolymers.a homologue of organic solvents as the organic modifier in mobile phase has also been explored. 相似文献
27.
以计量置换吸附理论(SDT A)为基础,从理论上推导出计量吸附模型中表征溶质对固定相亲合势大小的参数βa值与流动相中强置换剂浓度的对数呈线性关系。计量置换模型中的参数n和q(n和q分别代表1摩尔溶剂化溶质被吸附时,从吸附剂表面和从溶质分子表面所释放出的溶剂的物质的量)是计量置换参数Z值的分量,是两个非常有用的参数,可以从这个定量关系中直接获得。推导出的方程用苯的衍生物进行了实验验证,获得了较满意的结果。将这种方法计算得到的分量值与SDT A与计量置换保留模型(SDT R)相结合的方法得到的分量值进行了比较。 相似文献
28.
Norman O. Smith 《Journal of solution chemistry》1994,23(4):521-539
A method of finding the activity coefficients of salts, anhydrous or hydrated, in binary solid solutions, described in an earlier paper as it applies to continuous series, has been applied to discontinuous series. The salts must differ with respect to only one ion. The method requires isothermal distribution data for equilibria between liquid (aqueous) and solid solutions in the ternary system consisting of the two salts and water. The following salt pairs were used for illustration: K(I/Br) at 0, 15, 25, 35, and 50°C., (NH4/K)SCN at 0, 30, 60, and 90°C., (K/Tl)C103 at 10°C., and (NH4/K)SO3NH2, (NH4/K)Br, (Mg/Co)SO4-7H2O, and (Mn/Cu) SO4.n H2O-all at 25°C. Two kinds of behavior were noted and treated differently: systems in which the two series have the same, and those in which they have different crystal lattices. For two salts, A and B, which have the same lattice, and whose rational activity coefficients, f
A
and f
B
, can be described by 2-suffix Margules equations (regular solutions), lnf
A
=Bsx
B
2
and lnf
B
=Bsx
A
2
to be partially miscible, Bs>2, but this requirement does not apply if the lattices are different. In each series, distribution constants for the equilibria were also determined. Where possible, the calculated activities of the salts or the Gibbs excess energies of the solid solutions were compared with values reported by others who determined them by other methods. All the salt pairs studied show slight or strong positive deviations from ideality. 相似文献
29.
The binding constants, K′, for the reaction between some alkyldimethylbenzylammonium bromide homologues (alkyl = methyl, ethyl, propyl, butyl, hexyl,
decyl, and dodecyl, respectively) and β-cyclodextrin in water at 25.0 ± 0.1 ∘C have been determined, by applying the spectral displacement technique with phenolphthalein as the displacing anion. It has
been shown that the ln K′ values increase linearly with the number of carbon atoms in the alkyl chain for the salts whose alkyl chain has at least
four carbon atoms. The ln K′ values estimated for the parent compound benzyltrimetylammonium bromide and its two nearest homologues are distinctly lower
than might be expected by extrapolation of the linear relation found for the higher homologues. Assuming that it is the organic
cation that undergoes association with β-cyclodextrin, then one may suppose that a change occurs in the mode of inclusion of the cation upon passing to higher homologues.
In the case of the lighter homologues, it is the phenylene group that undergoes inclusion. This model of inclusion is confirmed
by analysis of rotating-frame overhauser effect spectroscopy (ROESY) spectra. 相似文献
30.
目的探讨经颈内静脉原位导丝法换置中心静脉长期血液透析导管在维持性血液透析(MHD)患者中的应用价值。方法选取近3年在颈内静脉留置的中心静脉长期血液透析导管因功能障碍后,并经颈内静脉原位导丝法换置长期导管,术后及每次透析后均改用尿激酶封管患者16例(原位换置组);选取同期首次经颈内静脉留置中心静脉长期血液透析导管,普通肝素封管患者20例作为对照组;分析两组患者围术期泵控血流量及随访期的反应及开存期率、次开存期率。结果围术期泵控血流量原位换置组高于对照组,有统计学差异(P<0.05);两组比较感染例次/1000导管日0.9%与1.0%,无统计学差异(P>0.05)。原位换置组围术期未发生中重度并发症,12个月开存期率81.2%、次开存期率93.8%;对照组开存期率为65%、次开存期率85%;两组比较无统计学差异(P>0.05)。结论颈内静脉原位导丝法换置中心静脉长期血液透析导管,在MHD患者中的使用是安全的、可行的。 相似文献