全文获取类型
收费全文 | 17034篇 |
免费 | 2815篇 |
国内免费 | 3129篇 |
专业分类
化学 | 13896篇 |
晶体学 | 288篇 |
力学 | 773篇 |
综合类 | 265篇 |
数学 | 1822篇 |
物理学 | 5934篇 |
出版年
2024年 | 17篇 |
2023年 | 291篇 |
2022年 | 407篇 |
2021年 | 571篇 |
2020年 | 690篇 |
2019年 | 712篇 |
2018年 | 596篇 |
2017年 | 594篇 |
2016年 | 815篇 |
2015年 | 884篇 |
2014年 | 1103篇 |
2013年 | 1486篇 |
2012年 | 1582篇 |
2011年 | 1649篇 |
2010年 | 1263篇 |
2009年 | 1119篇 |
2008年 | 1307篇 |
2007年 | 1220篇 |
2006年 | 1058篇 |
2005年 | 871篇 |
2004年 | 705篇 |
2003年 | 583篇 |
2002年 | 537篇 |
2001年 | 502篇 |
2000年 | 409篇 |
1999年 | 373篇 |
1998年 | 256篇 |
1997年 | 213篇 |
1996年 | 193篇 |
1995年 | 184篇 |
1994年 | 155篇 |
1993年 | 125篇 |
1992年 | 87篇 |
1991年 | 86篇 |
1990年 | 82篇 |
1989年 | 36篇 |
1988年 | 43篇 |
1987年 | 23篇 |
1986年 | 39篇 |
1985年 | 28篇 |
1984年 | 19篇 |
1983年 | 17篇 |
1982年 | 9篇 |
1981年 | 10篇 |
1980年 | 5篇 |
1979年 | 4篇 |
1976年 | 3篇 |
1974年 | 2篇 |
1973年 | 3篇 |
1957年 | 4篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
81.
82.
Here we present a novel design of electrochemical signal enhancer to increase the detection sensitivity of electrochemical DNA biosensors. The key element of this enhancer is a lysine‐rich peptide (LRP). Its C‐terminal is conjugated with a planer molecule, being able to intercalate into the base pairs of probe‐target duplexes. The lysine residues of LRP are covalently linked with electrochemical signal indicators, acting as an assembly of electrochemical signal indicators. Experimental results proved the feasibility of the novel design. We have examined the effects of the numbers of lysine residues and the hybridization conditions on the detection sensitivity. The optimization procedures have led to significant sensitivity enhancement, and the LOD (limit of detection) has been determined to be 1.4 amol. This enhancer demonstrates advantages of easy operation, simple instrumentation, and high exemption from environmental influence. 相似文献
83.
The Ramanujan Journal - We generalise Euler’s partition theorem involving odd parts and distinct parts for all moduli and provide new companions to... 相似文献
84.
Two new coordination complexes based on benzimidazole dicarboxylic acid, Zn(Hbidc)?H2O ( 1 ) and Cd(Hbidc)(H2O) ( 2 ), have been synthesized under hydrothermal conditions. The complexes were characterized using elemental analysis, infrared and UV–visible spectroscopies, powder X‐ray diffraction, thermogravimetry and single‐crystal X‐ray diffraction. Structural analyses showed that the crystal structures of 1 and 2 are different, due to the various modes of linking of the benzimidazole dicarboxylic acid. Complex 1 has a two‐dimensional network structure and 2 has a three‐dimensional network structure. In addition, we studied the performance of the fluorescence response of two complexes. Results showed that the complexes can be used as chemical sensors for multifunctional testing, such as for UO22+, xanthine and Fe3+ ions. Even if the concentration is very low, they could also be detected, showing that coordination complexes 1 and 2 have very high fluorescence sensitivity. The detection limit for UO22+ is 5.42 nM ( 1 ) and 0.02 nM ( 2 ), that for xanthine is 1.37 nM ( 1 ) and 0.28 nM ( 2 ), and that for Fe3+ ions is 0.76 nM ( 1 ) and 0.62 nM ( 2 ). 相似文献
85.
Mingyi Liu Shibo Huang Jinhua Wen Chunhua Xia Hong Zhang Yuqing Xiong 《Biomedical chromatography : BMC》2019,33(11)
Bicyclol is a synthetic drug widely used to treat chronic hepatitis B. This study aimed to develop a selective, sensitive and high‐throughput liquid chromatography–tandem mass spectrometric method for the detection of bicyclol in human plasma. Bicyclol was detected using a multiple reaction monitoring mode, with ammonium adduct ions (m/z 408.2) as the precursor ion and the [M‐CH3]+ ion (m/z 373.1) subjected to demethylation as the product ion. Chromatographic separation was achieved using a Zobax Eclipse XDB‐C18 column with a gradient elution and a mobile phase of 2 mm ammonium formate and acetonitrile. Bicyclol was extracted from plasma matrix by precipitation. A linear detection response was obtained for bicyclol ranging from 0.500 to 240 ng/mL, and the lower limit of quantification was 0.500 ng/mL. The intra‐ and inter‐day precisions were all ≤7.4%, and the accuracies were within ±6.0%. The extraction recovery was >95.9%, and the matrix effects were between 96.0% and 108%. Bicyclol was found to be unstable in human plasma at room temperature, but the degradation was minimized by conducting sample collection and preparation in an ice bath. The validated method was successfully applied to investigate the pharmacokinetics of bicyclol tablets in six healthy Chinese volunteers. 相似文献
86.
Yan‐Ping Zhang Yue Li Guan‐Cheng Xu Jin‐Yu Li Hua‐Ying Luo Jin‐Yao Li Li Zhang Dian‐Zeng Jia 《应用有机金属化学》2019,33(3)
Two new complexes, namely [Cu6L6] ( 1 ) and [Zn(HL)2] ( 2 ) (H2L = N‐(1‐phenyl‐3‐methyl‐4‐propenylidene‐5‐pyrazolone)‐2‐furancarboxylic acid hydrazide), have been synthesized and characterized. Single crystal X‐ray analysis indicates that complex 1 has a hexanuclear structure and complex 2 exhibits a mononuclear structure. The DNA/bovine serum albumin (BSA) binding properties of complexes 1 and 2 were investigated by absorption spectroscopy and fluorescence quenching. Both complexes could effectively intercalate to DNA with calculated quenching constants of 2.6 × 105 and 1.25 × 105 M?1, respectively. The quenching mechanism of the intrinsic fluorescence of BSA by the complexes was found to be a static one. The cytotoxicities of 1 and 2 were investigated in two human tumor cell lines, human esophageal cancer cells (Eca‐109) and cervical cancer cells (HeLa). Complex 1 exhibits higher antitumor activity than 2 . Furthermore, 1 can inhibit HeLa cells by inducing apoptosis and G0/G1 phase cell cycle arrest. All results demonstrate that 1 and 2 both have DNA/BSA binding capacity and antitumor activity. 相似文献
87.
88.
Mengmeng Ma Ying Wang Nan Gao Xinping Liu Yuhuan Sun Prof. Jinsong Ren Prof. Dr. Xiaogang Qu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(51):11852-11858
Proteolysis of amyloid-β (Aβ) is a promising approach against Alzheimer's disease. However, it is not feasible to employ natural hydrolases directly because of their cumbersome preparation and purification, poor stability, and hazardous immunogenicity. Therefore, artificial enzymes have been developed as potential alternatives to natural hydrolases. Since specific cleavage sites of Aβ are usually embedded inside the β-sheet structures that restrict access by artificial enzymes, this strongly hinders their efficiency for practical applications. Herein, we construct a NIR (near-IR) controllable artificial metalloprotease (MoS2-Co) using a molybdenum disulfide nanosheet (MoS2) and a cobalt complex of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (Codota). Evidenced by detailed experimental and theoretical studies, the NIR-enhanced MoS2-Co can circumvent the restriction by simultaneously inhibition of β-sheet formation and destroying β-sheet structures of the preformed Aβ aggregates in living cell. Furthermore, our designed MoS2-Co is an easy to graft Aβ-target agent that prevents misdirected or undesirable hydrolysis reactions, and has been demonstrated to cross the blood brain barrier. This method can be adapted for hydrolysis of other kinds of amyloids. 相似文献
89.
Yong-Li Li Qiang Zhang Jian-Jun Wu Li-Jun Xue Li-Ming Chen Jun-Mian Tian Zhuo-Ni Xu Ying Chen Xian-Wen Yang Xiao-Jiang Hao Jie Li 《Tetrahedron letters》2019,60(10):751-753
From Abies nukiangensis, two novel 13,14-seco-abietane diterpenes, nukiangendines A (1) and B (2) were isolated. Their relative structures were determined by extensive NMR and HRMS spectroscopic analysis. The absolute configuration of 1 was established by ECD calculations. Compound 1 showed significant anti-hepatitis C virus (HCV) effects. 相似文献
90.