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61.
固定化过氧化物酶在过氧化物测定中的应用 总被引:4,自引:0,他引:4
采用聚丙烯酰胺凝胶迭氮法固定了辣根过氧化物酶,其作为催化剂用于荧光法测定过氧化物,并探讨了固定酶测定过氧化物的最佳条件,如溶液pH值、温度、反应时间、荧光剂用量等。结果表明:酶固定化后,反应pH值范围变宽,为pH5.0-7.0和7.5-9.0,最佳pH为7.8左右;酶的热稳定性与储存稳定性也都得到提高,在室温下便可用固定酶进行长时间测定,且可较长时间保存。采用固定酶制成的酶柱用于HPLC测定过氧化物,固定酶可反复使用,简化了测定操作,并降低了成本。 相似文献
62.
Subbarayan Velusamy 《Tetrahedron letters》2005,46(22):3819-3822
Copper(II) complex 1 catalyzes the oxidation of sulfides to sulfoxides with 30% H2O2 in high yields. Addition of a catalytic amount of TEMPO to the reaction mixture enhances the conversion and selectivity. Complex 1 can be recycled without loss of activity. 相似文献
63.
A kinetic method for the determination of selenium(IV) traces is proposed, based on its inhibitory action on the oxidation of Nile Blue A by hydrogen peroxide in phosphate buffer (pH 10.5). A linear dependence was established between the rate of the proposed indicator reaction and selenium concentration in the range 9.5 × 10–2-1.58 ng cm–3. The experimental conditions of maximal selenium effect were established. Selenium, determined by the tangent method, was determined at concentrations over the range 0.22–1.26 ng cm–3, with relative standard deviations up to 4.5%. The reaction rate was followed spectrophotometrically. The effect of foreign ions on the accuracy of this method was also investigated. The method was applied to the determination of selenium in pharmaceutical preparations and wheat flour. 相似文献
64.
Zong Yuan Chen Wei Zhang 《中国化学快报》2007,18(12):1443-1446
A simple method for the oxidative aromatization of Hantzsch 1,4-dihydropyridines to the corresponding pyridines is achieved by using hydrogen peroxide as green oxidant and acetic acid as catalyst in aqueous solution. 相似文献
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67.
深入研究了C60 与全氟酰基过氧化物的反应 ,通过变温EPR测试证实了此反应的自由基加成机理 .用色谱分析并结合产物的19FNMR结构鉴定 ,首次发现由于加成过程中发生的全氟烷基自由基的 β Scission ,生成了新的氟烷基自由基 ,从而生成了多种氟烷基化的C60 .表面性能研究发现氟烷基化的C60 具有优良的疏水、疏油性 .总之 ,利用C60 与全氟酰基过氧化物的反应 ,成功地对C60 进行了全氟烷基化修饰 相似文献
68.
O. I. Dyubchenko V. V. Nikulina E. I. Terakh A. E. Prosenko I. A. Grigor’ev 《Russian Chemical Bulletin》2007,56(6):1149-1155
The reaction of ω-(4-hydroxyaryl)haloalkanes with various nitrogen-containing agents afforded primary, secondary, and tertiary
amino derivatives of 2,6-dialkylphenols. For the compounds synthesized, the reaction rate constants with peroxide radicals
were measured for cumene and methyl oleate oxidation. The total inhibitory activity in the model reactions of thermal autooxidation
of lard and hexadecane was studied. The rate constants of alkyl(hydroxylaryl)amines are the same as those of the corresponding
alkylphenols, whereas the total inhibitory activity of some alkyl(hydroxylaryl)amines exceeds substantially that for alkylphenols.
Dedicated to the memory of Academician N. N. Vorozhtsov on the 100th anniversary of his birth.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1107–1112, June, 2007. 相似文献
69.
电沉积AuInSe2半导体薄膜上的电化学振荡现象 总被引:1,自引:0,他引:1
研究了电沉积制得的AuInSe2半导体薄膜上过氧化氢阴极还原过程中产生的电化学振荡行为,对影响该振荡行为的一些因素如半导体薄膜的后处理、溶液组成、传质、光照、化学浸渍作用等进行了分析,同时采用外界周期性光照和外接小幅度正弦波电位来调节振荡频率,为金铟硒半导体薄膜发展成为光电传感器件提供了一定的理论与实践基础. 相似文献
70.
Hidetake Sakuraba Hiroshi Maekawa 《Journal of inclusion phenomena and macrocyclic chemistry》2006,54(1-2):41-45
The two modified β-cyclodextrin (β-CD) derivatives having catechol-type ligand (2,3- and 3,4-dihydroxy groups on the benzoate
ring) were synthesized. The chiral catalytic activity of their MoV and CuII complexes was examined in the asymmetric oxidation of aromatic sulfides using hydrogen peroxide in water (pH 6.0). The oxidation
with the MoV complexes of two β-CD derivatives were more accelerated than that with the CuII complexes. The sign of the optical rotation of the sulfoxides obtained in the above two cases showed the opposite configuration
in the oxidation of the same sulfide. The difference of the enantioselectivity appeared also between the two complexes of
the 2,3- and 3,4-dihydroxybenzoate derivatives with the same metal ion. While the use of the MoV complexes with the catechol derivatives yielded the sulfoxides with 35–65% ee, the use of the CuII complexes gave the products with the␣opposite configuration at 26–52% ee. The chiral induction in the oxidation, observed
conversely between the␣catalysts, was reflected on the chiral conformation of the respective metal catalysts, showed in Induced
Circular Dichroism (ICD) spectra. The highest optical yield, 65%, was observed in the oxidation of butyl phenyl sulfide using
the catalytic amount (0.1 equiv) of the MoV complex with mono-6-O-(3,4-dihydroxybenzoyl)-β-CD. The reaction gave predominantly the (S)-sulfoxide in 95% chemical yield. 相似文献