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991.
共轭亚麻酸的制备、表征和生物活性研究进展 总被引:2,自引:0,他引:2
近年来的研究发现共轭亚麻酸(CLN)具有多种非常有益的生理功能,已成为化学家、药理学家、营养学家争相研究的热点。本文就CLN的制备、表征、分离分析以及生物活性等方面,对国内外的研究进行了综述。CLN的制备包括化学法、生物法和天然产物提取法三大类。CLN的表征方法主要有紫外光谱、红外光谱、核磁共振等方法,以及采用气相色谱法(GC)、高效液相色谱法(HPLC)和毛细管电泳法(CE)等方法对合成的CLN混合物进行分离分析。CLN的生物活性主要有抗癌、降血脂、减肥、抗致癌等。 相似文献
992.
993.
Kariate Sudhakara Prasad A. B. Arun P. D. Rekha Chiu‐Chung Young Jen‐Lin Chang Jyh‐Myng Zen 《Electroanalysis》2009,21(14):1646-1650
Aerobically grown Shewanella sp. bacterial suspension drop‐coated on a disposable screen‐printed carbon electrode was found to possess electroactivity without the aid of redox mediator. Cyclic voltammetric studies revealed the characteristics of a mixed diffusion adsorption‐controlled electrochemical process for direct electron transfer at the bacteria‐modified electrode. Both FE‐SEM and ATR FT‐IR experiments were carried out to investigate the surface characteristics. The electroanalytical applicability was further demonstrated for electrocatalytic reduction of arsenite, hydrogen peroxide and nitrite. Low cost and very simple manufacturing procedure allow for the proposed bacterial sensor to be applied as disposable devices. 相似文献
994.
改性柑橘果胶的制备、表征及抗癌活性 总被引:2,自引:0,他引:2
采用琼脂糖凝胶电泳、比旋度测试、HPSEC-RID、IR、1H NMR、13C NMR、高碘酸氧化及甲基化分析等手段对改性柑橘果胶(MCP)进行了分析, 结果表明, MCP是一种均一性多糖, 分子量约为21000~66000, 糖醛酸质量分数为81.0%, 酯化度为2.13%. MCP的中性单糖残基主要包括鼠李糖(Rha)、阿拉伯糖(Ara)、木糖(Xyl)和半乳糖(Gal)等, 其摩尔比约为1.0∶1.5∶1.4∶1.3, 主链包括HG和RG, 分支结构含有末端Gal, Xyl和Ara. 选用3种小鼠移植性肿瘤模型对MCP的抗肿瘤生长活性进行研究. 结果表明, MCP对肝癌H22细胞有较强抑制作用, 高剂量下抑制率可达47.8%; 对宫颈癌U14细胞的抑制率在高剂量及中等剂量下分别达到36.5%和38.5%; 对肉瘤S180没有抑制活性. MCP的抗肝癌和抗宫颈癌活性为首次发现. 相似文献
995.
996.
利用溶胶-凝胶方法合成了Ce0.8Pr0.2O2-δ固溶体, XRD结果表明,经200 ℃焙烧就已经形成立方萤石结构固溶体,晶粒尺寸为8.1 nm, 随焙烧温度的升高,晶粒尺寸增大. X射线光电子能谱(XPS)结果表明,样品中存在氧离子缺位,铈离子主要为Ce4 离子,镨离子以混合价态Pr3 和Pr4 存在. 固溶体Ce0.8Pr0.2O2-δ的拉曼谱(Raman)观察到4个峰,458和1140 cm-1峰为特征F2g振动谱带,较宽的570和187 cm-1峰对应氧离子缺位及引起的不对称振动. 交流阻抗谱表明固溶体Ce0.8Pr0.2O2-δ在600 ℃时的电导率为1.44×10-3 S·cm-1, 活化能为Ea=0.67 eV (650~800 ℃), Ea=0.91 eV (400~600 ℃). 相似文献
997.
Xiaoli He Sen Lin Xuan Guo Lude Lu Xin Wang Xujie Yang 《Frontiers of Chemistry in China》2008,3(4):413-417
Three tetraorganodistannoxanes containing silicon were synthesized and their catalytic properties in esterification and acetalization
were observed via the reactions of acetic acid with isoamyl alcohol and butyraldehyde with glycol. The factors affecting the reaction, such
as the catalyst dosage, reaction time and solvent, etc. were discussed. The results show that the three tetraorganodistannoxanes
displayed similar good catalytic activities compared to dichlorotetrabutyldistannoxane in esterification and acetalization.
When the dosage of [ClBu2SnOSn-(CH2SiMe3)2Cl]2 was 1.5% based on the mass of reactant, the yield of isoamyl acetate was 91.8% and the yield of butyraldehyde glycol acetal
94.2%. The different alkyl and bridging groups on Sn sites in the structure of tetraorganodistannoxanes showed some influence
on the catalytic activities of these compounds.
__________
Translated from Chinese Journal of Applied Chemistry, 2007, 24 (11): 1265–1272 相似文献
998.
Xiu-Li Wang Hong-Yan Lin Guo-Cheng Liu Hai-Yan Zhao Bao-Kuan Chen 《Journal of organometallic chemistry》2008,693(16):2767-2774
Two novel coordination polymers [Cu3(1,3-BDC)4(Dpq)2] (1) and [Cu2(BTC)(OH)(Dpq)2] · H2O (2), have been hydrothermally synthesized by self-assembly of aromatic polycarboxylate ligands 1,3-H2BDC (1,3-H2BDC = 1,3-benzenedicarboxylate) or H3BTC (H3BTC = 1,3,5-benzenetricarboxylate), chelating ligand Dpq (Dpq = dipyrido[3,2-d:2′,3′-f]quinoxaline), and copper chloride. X-ray diffraction analysis reveals that each trinuclear CuII cluster is bridged by two coordination modes of 1,3-BDC ligands to form one-dimensional (1-D) chain structure in complex 1. Complex 2 possesses a two-dimensional (2-D) layer network composed of dinuclear [Cu2(OH)(Dpq)2] unit and bridging ligand BTC. The adjacent chains for 1 or the adjacent layers for 2 are further linked by π-π stacking interactions to form the three-dimensional (3-D) supramolecular frameworks. Moreover, the electrochemical properties of the two copper(II) complexes bulk-modified carbon paste electrodes (Cu-CPEs: 1-CPE and 2-CPE) have been studied, and the results indicate that both Cu-CPEs give one-electron quasi-reversible redox waves in potential range of 600 to −400 mV due to the metal copper ion Cu(II)/Cu(I). The Cu-CPEs have good electrocatalytic activities toward the reduction of nitrite and bromate in 0.1 M pH 2 phosphates buffer solution, and have remarkable long term stability and especially good surface renewability by simple mechanical polishing in the event of surface fouling, which is important for practical application. 相似文献
999.
The sensitivity as well as dynamic range of a ratiometric probe is determined by the ratio of emission intensities at two wavelengths. Thus, it is highly desirable to acquire a large ratiometric fluorescence response at two wavelengths. However, ratiometric fluorescent signals are intrinsic characteristics of the particular probe-analyte interactions. The design for fluorescent probes with a large ratiometric signal remains a challenging task. There is still a lack of a proper approach to enhance the ratiometric fluorescence response for fluorescent chemodosimeters. Herein, we introduced a novel strategy to increase the emission ratios of a chemodosimeter via modulation of intramolecular charge transfer. 相似文献
1000.
First examples of transition metal complexes with HpicOH [Cu(picOH)2(H2O)2] ( 1 ), [Cu(picO)(2,2′‐bpy)]·2H2O ( 2 ), [Cu(picO)(4,4′‐bpy)0.5(H2O)]n ( 3 ), and [Cu(picO)(bpe)0.5(H2O)]n ( 4 ) (HpicOH = 6‐hydroxy‐picolinic acid; 2,2′‐bpy = 2,2′‐bipyridine; 4,4′‐bpy = 4,4′‐bipyridine; bpe = 1,2‐bis(4‐pyridyl)ethane) have been synthesized and characterized by single‐crystal X‐ray diffraction. The results show that HpicOH ligand can be in the enol or ketonic form, and adopts different coordination modes under different pH value of the reaction mixture. In complex 1 , HpicOH ligand is in the enol form and adopts a bidentate mode. While in complexes 2 – 4 , as the pH rises, HpicOH ligand becomes in the ketonic form and adopts a tridentate mode. The coordination modes in complexes 1 – 4 have not been reported before. Because of the introduction of the terminal ligands 2,2′‐bpy, complex 2 is of binuclear species; whereas in complexes 3 and 4 , picO ligands together with bridging ligands 4,4′‐bpy and bpe connect CuII ions to form 2D nets with (123)2(12)3 topology. 相似文献