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61.
J. C. Evans K. R. N. Rao S. K. Jackson C. C. Rowlands M. D. Barratt 《Journal of separation science》1985,8(12):829-830
Radicals generated in linoleic acid and deuterated linoleic acid have been trapped by the spin trap 2-methyl-2-nitroso-propane (MNP) and identified by electron spin resonance (ESR) and ENDOR spectroscopy. The formation of two distinct secondary alkyl radical adducts (one conjugated, the other non-conjugated, as shown by their UV absorption spectra) was demonstrated by 11, 11-dideuterio-9-cis-12-cis-linoleic acid using HPLC and ESR spectroscopy. 相似文献
62.
采用低湿溶液缩聚的方法合成了对苯二甲酰氯,二甲基联苯胺和己二醇为单体的芳酯族液晶聚酯酰胺。用DSC,X光衍射分析和偏光显微镜等手段研究了该系列聚酯酰胺的热致液晶行为,确认了二甲基联苯胺单体用量在20%(mol)的情况下,所得聚酯酰胺仍为向列型液晶聚合物。由于聚酯酰胺分子间聚酰胺链段之间的氢键作用,随着二甲基联苯胺用量增加至60mol%时,所得的聚酯酰胺己无液晶转变温度,其液晶区间即从熔融温度直至分 相似文献
63.
The solubilization of benzo[a]pyrene by organic solvents (dioxane, toluene and dichloromethane) and a surfactant (Triton X-100) was investigated. These media were successfully used for the determination of benzo[a]pyrene using fluorescence detection, with excellent limits of detection and large linear analytical ranges. Benzo[a]pyrene was detected in coal washing waters using liquid chromatography with fluorescence detection. The stability of this compound in dioxane was also examined. 相似文献
64.
Low molecular weight tri-podal biphenyl- and benzoate-type mesogens [C6H5C6H4O(CH2)5SiMe2CH2CH2SiMe2]3CH (4), [C11H23O(C6H4)2O(CH2)5SiMe2]3CH (5) and [MeOC6H4OC(O)C6H4O(CH2)5SiMe2]3CH (6) (C6H4 = 1,4-phenylene) were obtained, from branched silyl substituted methane precursors [CH2CH(Me)2Si]3CH (1) and (HMe2Si)3CH (2). The biphenyl-containing ones (4) and (5) were converted into terminal alkenes, which were subsequently hydrosilylated with poly(methylsiloxanes). The polymer derived from (5) exhibited mesomorphic properties. Such systems have the potential to significantly increase the density of liquid crystal rod-like structures in side chains of linear polymers (or dendritic liquid crystal polymers). 相似文献
65.
Dielectric studies have been performed at elevated pressures on two compounds of a homologous series possessing a strongly polar terminal group and three phenyl rings in their molecular structure. This is the first high pressure dielectric study on such systems that exhibit a monolayer smectic A phase. Also notable is the fact that these compounds show a dual frequency response, a promising feature for fast liquid crystal display devices. The low frequency relaxation recorded in the nematic and smectic A phases is attributed to the reorientation of the molecules about the short axis. The temperature and pressure dependence of the relaxation frequency of this mode as well as the involved activation parameters are discussed. At a given relative temperature the relaxation frequency decreases as the pressure is increased. However, the parameter that characterizes the temperature dependences of the relaxation frequency, viz., the activation enthalpy, has a very weak dependence on pressure. In contrast, the activation volume shows a linear decrease with temperature. 相似文献
66.
Shi-jun Zheng Kazuo Akagi Qun Xu Shao-kui Cao Qi-feng Zhou 《高分子科学》2006,(4):353-361
Novel shish-kebab type liquid crystalline poly(p-phenylenevinylene) derivatives were synthesized by Stille coupling reaction from 2,5-bis[(4-n-alkoxyl)benzoyloxy]1,4-dibromobenzene (monomer l) and 1,2-bis(tributylstannyl) ethylene (monomer 2). The polymers with alkoxy groups are soluble in common organic solvents and exhibit blue fluorescence. Both the cast film and the annealed film have large red-shifts in fluorescence spectra and show yellow fluorescence. The polymers with CN and NO2 groups show poor solubility and green fluorescence. All the polymers possess liquid crystalline smectic phases. The melting point (Tm) of the polymers decreases when the length of the alkoxy tails of the mesogenic units increases. The polymers are easily aligned under a magnetic field of 10 Tesla. It is found that the conjugated backbone and LC side chain are aligned perpendicular and parallel to the magnetic field, respectively. The polymers show optical dichroism in fluorescence spectra, suggesting that they are available for advance materials with linear optical polarization. 相似文献
67.
W/O/W乳液的渗透溶胀与夹带溶胀 总被引:6,自引:0,他引:6
研究了W/O/W乳液的溶胀,实验结果表明,渗透溶胀随内外相溶液间的渗透压差、表面活性剂及载体浓度的增大而增加,但随膜粘度的增加而降低,渗透压差较高时,水渗透的影响大于夹带的影响;膜相中含氧化合物对溶胀的影响大于含氮化合物,采用Span 80作乳化剂时,比采用E 644渗透溶胀约高6倍,夹带溶胀也较高;重复聚结再分散使夹带溶胀急剧增加,因而多级混合澄清槽对液膜操作似不适用。 相似文献
68.
A. N. Ageev A. A. Aratskova L. D. Belyakova T. N. Gvozdovich A. V. Kiselev Ya. I. Yashin J. Kàlal F. Švec 《Chromatographia》1983,17(10):545-548
Summary The retention of benzene derivatives with nonpolar and polar substituents on a porous methacrylate copolymer containing epoxy groups using both nonpolar and polar eluents was investigated. When n-hexane is used as the eluent, the retention of n-alkylbenzenes and polymethylbenzenes is weaker than that of benzene. In the case of benzene derivatives containing polar functional groups their capacity ratios (k) on this porous polymer increases approximately linearly with the increase of the adsorbate molecules dipole moment. The retention characteristics of the methacrylate copolymer were compared with that of a styrene-divinylbenzene copolymer and silica gels with a hydroxylated surface and with a surface modified by chemically bonded alkylsilyl groups. 相似文献
69.
Ben-zhong Tang Xiang-xing Kong Xin-de Feng Department of Chemistry Hong Kong University of Science & Technology Clear Water Bay Kowloon Hong Kong China Department of Polymer Science & Engineering College of Chemistry Peking University Beijing China 《高分子科学》1999,(3):289-294
A new liquid crystalline polyacetylene containing a phenyl benzoate mesogen (5) is synthesized,whose mesomorphic properties are found to be easily "tunab1e" by simple mechanical perturbation. Thepolymerization of 10- [ 4 - (4' -methoxyphenoxycarbonyl )phenoxycarbonyl] - 1 -decyne (4 ) in itiated by theWCl_6-Ph_4Sn/dioxane complex yields polymer 5 with a M_w of 28400. The molecular structure of 5 ischaracterized by NMR, IR, and UV spectroscopy and its liquid crystalline behavior is investigated by DSC,POM, and XRD analysis. Upon mechanical perturbation, 5 exhibits unusual agitation-induced high-strengthdisclinations, shear-induced inversion walls, and solidification-induced banded textures. Such phenomenahave been observed in the main-chain liquid crystalline polymers with rigid backbones, but have seldom beenreported for the side-chain liquid crystalline polymers with flexible backbones, suggesting that the rigidpolyacetylene backbone of 5 plays a constructive role in inducing the novel molecular alignments. 相似文献
70.
Molecular mobility in thermotropic polyesters and side-chain polymers with different struc-ture of mesogens and spacers has been studied by dielectrical method in dilutesolutions. The results made it possible to establish the multiplicity of dielectric relaxationtransitions which reflects the small- and large-scale types of molecular motion. It was shownthat dielectric relaxation processes occurring in accordance with local mechanism (relaxationtimes 10~(-9)--10~(-7)s. and the activation energy 10--50kJ/mol) are due to the mobility of kineticchain elements of different length within a monomer units. It was found that the dielectricrelaxation process connected with a large-scale form of molecular motion (relaxation times10~(-5)--10~(-6)s. and the activation energy 100kJ/mol) did not depend on the molecular massbut was infiuenced by factors changing the conformational state of the macromolecule. It isestablished tha the cooperative reorientation mobility of associated mesogenic fragments isthe source of the large-scale process. 相似文献