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991.
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A novel hydrated cobalt tetraborate complex NH4[Co(NH3)5(H2O)][B4O5(OH)4]2·6H2O, was synthesized by the reaction of NH4‐borate aqueous with CoCl2 and its structure was determined by single crystal X‐ray diffraction. The crystal system of this complex is orthorhombic, the space group is Pnma, and the unit cell parameters are a=1.2901(2) nm, b=1.6817(3) nm, c=1.1368(2) nm, α=β=γ=90°, V=2.4742(8) nm3, and Z=4. This compound contains infinite borate layers constructed from [B4O5(OH)4]2? units via hydrogen bonds. The adjacent polyborate anion layers are further linked together with the octahedral [Co(NH3)5(H2O)]3+ groups through hydrogen bonds to form 3D framework. The groups and guest water molecules are deposited in the empty space of this framework and interact with the layers by extensive hydrogen bonds. Infrared and Raman spectra (4000–400 cm?1) of NH4[Co(NH3)5(H2O)][B4O5(OH)4]2·6H2O were recorded at room temperature and analyzed. Fundamental vibrational modes were identified and band assignments were made. The middle band observed at 575 cm?1 in Raman spectrum is the pulse vibration of [B4O5(OH)4]2?. 相似文献
995.
996.
Zhang G Wang L Fu P Hu M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,82(1):424-431
The mechanism and conformational changes of farrerol binding to bovine serum albumin (BSA) were studied by spectroscopic methods including fluorescence quenching technique, UV–vis absorption, circular dichroism (CD) spectroscopy and Fourier transform infrared (FT-IR) spectroscopy under simulative physiological conditions. The results of fluorescence titration revealed that farrerol could strongly quench the intrinsic fluorescence of BSA through a static quenching procedure. The thermodynamic parameters enthalpy change and entropy change for the binding were calculated to be −29.92 kJ mol−1 and 5.06 J mol−1 K−1 according to the van’t Hoff equation, which suggested that the both hydrophobic interactions and hydrogen bonds play major role in the binding of farrerol to BSA. The binding distance r deduced from the efficiency of energy transfer was 3.11 nm for farrerol–BSA system. The displacement experiments of site markers and the results of fluorescence anisotropy showed that warfarin and farrerol shared a common binding site I corresponding to the subdomain IIA of BSA. Furthermore, the studies of synchronous fluorescence, CD and FT-IR spectroscopy showed that the binding of farrerol to BSA induced conformational changes in BSA. 相似文献
997.
Sargaeva NP Lin C O'Connor PB 《Journal of the American Society for Mass Spectrometry》2011,22(3):480-491
Ion-electron reaction based fragmentation methods (ExD) in tandem mass spectrometry (MS), such as electron capture dissociation
(ECD) and electron transfer dissociation (ETD) represent a powerful tool for biological analysis. ExD methods have been used
to differentiate the presence of the isoaspartate (isoAsp) from the aspartate (Asp) in peptides and proteins. IsoAsp is a
β3-type amino acid that has an additional methylene group in the backbone, forming a Cα–Cβ bond within the polypeptide chain. Cleavage of this bond provides specific fragments that allow differentiation of the isomers.
The presence of a Cα–Cβ bond within the backbone is unique to β-amino acids, suggesting a similar application of ExD toward the analysis of peptides
containing other β-type amino acids. In the current study, ECD and ETD analysis of several β-amino acid containing peptides
was performed. It was found that N–Cβ and Cα–Cβ bond cleavages were rare, providing few c and z type fragments, which was attributed to the instability of the Cβ radical. Instead, the electron capture resulted primarily in the formation of a and y fragments, representing an alternative fragmentation pathway, likely initiated by the electron capture at a backbone amide
nitrogen protonation site within the β amino acid residues. 相似文献
998.
Jingsong Sun Lin Liang Jianmin Sun Yanqiu Jiang Kaifeng Lin Xianzhu Xu Runwei Wang 《Catalysis Surveys from Asia》2011,15(1):49-54
This short review presents the recent developments in the direct synthesis of cyclic carbonates from olefins and CO2. The straightforward synthesis of cyclic carbonates from olefins instead of epoxides, also called one-pot “oxidative carboxylation”
of olefins, can be viewed as the coupling of two sequential reactions of epoxidation of olefins and CO2 cycloaddition to epoxides formed. The facile synthetic approach would make carbonate synthesis simpler and even cheaper with
industrial potential from environmental and economic points of view. Some progresses have been made on this direct synthetic
reaction for cyclic carbonates with homogeneous and heterogeneous catalysts, however, this reaction system is still at a preliminary
stage. Among the catalysts reported, only a few can be considered as effective for the direct oxidative carboxylation of olefins
to cyclic carbonates. Thus active and selective catalysts should be explored to put the direct synthesis of cyclic carbonates
into practical applications. 相似文献
999.
液相色谱-三重串联四极杆质谱测定粮油中的黄曲霉毒素 总被引:5,自引:0,他引:5
建立了超声提取-液相色谱-电喷雾三重串联四极杆质谱测定玉米、大米、大豆等粮油固体样品中黄曲霉毒素B1、B2、G1和G2(AFB1、AFB2、AFG1和AFG2)的方法。分析前对样品进行超声提取,优化得到最佳超声提取条件: 溶剂为甲醇-水(含40 g/L NaCl) (80:20, v/v)溶液、料液比为1:3(g:mL)、温度为50 ℃、时间为3 min。然后对提取的样品进行免疫亲和特异性净化。最后与液相色谱-电喷雾三重串联四极杆质谱联用,使用C18反相色谱柱,流动相为甲醇-10 mmol/L乙酸铵水溶液梯度洗脱,以黄曲霉毒素M1(AFM1)作为内标进行定量测定。结果表明,AFB1、AFB2、AFG1和AFG2的检出限分别为0.002、0.004、0.004和0.012 μg/kg。方法的加标回收率为87%~111%,日内相对标准偏差(RSD)和日间RSD分别不大于6.7%和5.6%。实验结果表明该方法可以有效地降低基质效应的影响,相比于外标法能极大地提高方法的准确度。 相似文献
1000.