全文获取类型
收费全文 | 293篇 |
免费 | 26篇 |
国内免费 | 39篇 |
专业分类
化学 | 225篇 |
力学 | 37篇 |
综合类 | 4篇 |
数学 | 37篇 |
物理学 | 55篇 |
出版年
2023年 | 9篇 |
2022年 | 8篇 |
2021年 | 14篇 |
2020年 | 12篇 |
2019年 | 8篇 |
2018年 | 8篇 |
2017年 | 11篇 |
2016年 | 12篇 |
2015年 | 20篇 |
2014年 | 17篇 |
2013年 | 15篇 |
2012年 | 15篇 |
2011年 | 20篇 |
2010年 | 18篇 |
2009年 | 8篇 |
2008年 | 15篇 |
2007年 | 12篇 |
2006年 | 11篇 |
2005年 | 5篇 |
2004年 | 8篇 |
2003年 | 5篇 |
2002年 | 14篇 |
2001年 | 23篇 |
2000年 | 7篇 |
1999年 | 10篇 |
1998年 | 8篇 |
1997年 | 4篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1994年 | 5篇 |
1993年 | 4篇 |
1992年 | 6篇 |
1991年 | 6篇 |
1990年 | 1篇 |
1989年 | 4篇 |
1988年 | 1篇 |
1986年 | 2篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1980年 | 1篇 |
1976年 | 1篇 |
1974年 | 1篇 |
1971年 | 1篇 |
排序方式: 共有358条查询结果,搜索用时 10 毫秒
31.
Ai‐Ting Xing Jun‐Mian Tian Chun‐Mei Liu Hui‐Liang Li Wei‐Dong Zhang Lei Shan 《Helvetica chimica acta》2010,93(4):718-723
Three new monoterpene alkaloids, mairine A ( 1 ), mairine B ( 2 ), and mairine C ( 3 ), and a new caffeic acid ester, 2‐(1‐hydroxy‐4,4‐dimethoxycyclohexyl)ethyl caffeate ( 4 ), were isolated from the EtOH extract of the whole plants of Incarvillea mairei var. multifoliolata. The structures of these compounds were established on the basis of 1D‐ and 2D‐NMR and HR‐ESI‐MS analysis. 相似文献
32.
β-淀粉样肽的结构、合成与性质及其与老年痴呆症的关系 总被引:3,自引:0,他引:3
β-淀粉样肽是β-淀粉样前体蛋白的剪切产物,分别由39-43个氨基酸残基组成。本文介绍了β-淀粉样肽的化学结构、化学合成及β-淀粉样肽与老年痴呆症的关系。 相似文献
33.
Two new pyrrolizidines named lankongensisine A (1), B (2) were isolated from the roots of Ligularia lankongensis collected in Lijiang, Yunnan, and their structures were established by spectroscopic analysis. 相似文献
34.
Seven new alkaloids, named as 1,9-epoxy-9a-hydroxystenine (1), tuberostemoline A (2), tuberostemoline B (3), tuberostemoninol C (4), oxotuberostemonine A (5), the mixture of bisdehydrotuberostemonine D (6), and bisdehydrotuberostemonine E (7), together with four known alkaloids neotuberostemonine (8), sessilifoline B (9), stemoxazolidinone F (10), and tuberostemoninol A (11), were isolated from the roots of Stemona tuberosa. The structures of 1–7 were elucidated through extensive spectroscopic analysis, and the relative configurations of 1–6 and 8 were further confirmed by X-ray crystallographic data. Compounds 8, 9 and the mixture of 6 & 7 exhibited potential acetylcholinesterase (AChE) inhibitory activities. 相似文献
35.
Hua-Hua Wang Yi-Yu Jiang Mian HR Mahmood Hai-Yang Liu Herman H.Y. Sung Ian D. Williams Chi K. Chang 《中国化学快报》2015,26(5):529-533
Tetrakis(alloxycarbonyl)porphyrin and its β-octafluoro-substituted derivatives were synthesized via Lindsey method and transformed to their zinc complexes.Single crystal X-ray structures of corresponding Zn(Ⅱ) porphyrins revealed that β-octafluorination will give more compactness of porphyrin moieties in the crystal structure owing to the hydrogen bonding interactions involving β-fluorine atoms.An unusual six-coordinated Zn(Ⅱ) was found via intramolecular coordination of oxygen atom of meso-substituents with central Zn(Ⅱ). 相似文献
36.
A facile, effective, and environmentally friendly method has been adopted for the first time to prepare tiny Co3O4 nanocrystals embedded carbon matrices without using surfactants, harmful organic reagents or extreme conditions. Structural characterizations reveal that the size-controlled Co3O4 nanocrystals are uniformly dispersed on carbon matrices. Electrochemical measurements reveal that Co3O4-ordered mesoporous carbon (OMC) can more efficiently catalyze glucose oxidation and acquire better detection parameters compared with those for the Co3O4-macroporous carbon, Co3O4-reduced graphene oxide, and free Co3O4 nanoparticles (NPs) (such as: the large sensitivity (2597.5 μA cm−2 mM−1 between 0 and 0.8 mM and 955.9 μA cm−2 mM−1 between 0.9 and 7.0 mM), fast response time, wide linear range, good stability, and surpassingly selective capability to electroactive molecules or Cl−). Such excellent performances are attributed to the synergistic effect of the following three factors: (1) the high catalytic sites provided by the uniformly dispersed and size-controlled Co3O4 nanocrystals embedded on OMC; (2) the excellent reactant transport efficiency caused by the abundant mesoporous structures of OMC matrix: (3) the improved electron transport in high electron transfer rate (confinement of the Co3O4 NPs in nanoscale spaces ensured intimate contact between Co3O4 nanocrystals and the conducting OMC matrix). The superior catalytic activity and selectivity make Co3O4-OMC very promising for application in direct detection of glucose. 相似文献
37.
Eight mono-reactive and four bis-reactive 2,3-epoxy/3-chloro-2-hydroxy propyl derivatives of quaternary ammonium salts have been synthesised by reacting epichlorohydrin with suitable tertiary amines and diamines. Mono-reactive derivatives also contain cyano and carboxylic groups in addition to 2,3-epoxy/3-chloro-2-hydroxy propyl groups. The structures of these quaternary ammonium salts have been characterised using IR and 1H NMR spectroscopic techniques. These quaternary ammonium chlorides have been applied to the cotton fabrics as pretreatments and aftertreatments and promising results have been obtained. 相似文献
38.
Mian Fu Xiaomei Zhuang Tianhong Zhang Ying Guan Qingbin Meng Yongjun Zhang 《Macromolecular bioscience》2020,20(9)
Leuprolide has been widely used in androgen deprivation therapy for the treatment of advanced prostate cancer, but its use is still limited due to its short half‐life. Herein, hydrogen‐bonded layer‐by‐layer films are fabricated from PEGylated leuprolide (PEG‐LEU) and tannic acid (TA). Because of its dynamic nature, the film disintegrates gradually in water and releases PEG‐LEU and TA. The in vitro release profile indicated perfect zero‐order kinetics, which is explained by the unique release mechanism. When implanted subcutaneously in male rats, the films maintain a constant serum drug level. For a 60‐bilayer film, the serum drug level is maintained constant for ≈24 days. No initial burst release is observed, suggesting that the in vivo release also follows zero‐order kinetics. Initially, an increase in the level of serum testosterone is induced by the released drug, followed by testosterone suppression to a constant level below the castrate level, which could be maintained as long as a constant serum drug level is maintained. Since the new drug carriers avoid an initial burst release of the drug and maintain a constant serum drug level and hence a constant serum testosterone level below the castrate level, these carriers are highly promising for androgen deprivation therapy. 相似文献
39.
Xiao-Xu Ba Tian Gao Mian Yang Peng Jiang Feng-Lei Jiang Yi Liu 《Journal of solution chemistry》2020,49(1):100-116
As one of the newly emerged nanomaterials, graphene quantum dots (GQDs) have shown great application potential as tracking probes and drug carriers in biological areas. The GQDs synthesized via the nitric acid reflux method in this study turned out to quench the fluorescence of human serum albumin (HSA) and gamma globulin (γ-globulin) in two different functional ways. The fluorescence quenching effect of GQDs on HSA is a static pattern and the predominant interaction forces are hydrogen bonds and van der Waals forces. Distinct from HSA, the interaction between GQDs and γ-globulins belongs to dynamic quenching and is driven by electrostatic forces. Ultraviolet–visible (UV–vis) differential spectrometry and transient state fluorescence spectrometry were also utilized to further confirm their quenching types. Also, thermodynamics parameters, the enthalpy change (ΔH) and entropy change (ΔS) of reaction between GQDs and proteins were obtained through a series of calculations from the van’t Hoff equation. Furthermore, the effect of GQDs on the conformational structure of proteins was characterized by synchronous fluorescence spectra (SFS), three-dimensional (3D) fluorescence and circular dichroism (CD) spectra. In addition, the binding mechanism of GQDs with HSA and γ-globulins were proposed based on the obtained experimental results. The research on the reaction between GQDs with HSA and γ-globulins offers promising insight for the further application of nanomaterials in biomedical fields. 相似文献
40.