全文获取类型
收费全文 | 3060篇 |
免费 | 580篇 |
国内免费 | 318篇 |
专业分类
化学 | 1871篇 |
晶体学 | 4篇 |
力学 | 36篇 |
综合类 | 39篇 |
数学 | 254篇 |
物理学 | 655篇 |
无线电 | 1099篇 |
出版年
2024年 | 32篇 |
2023年 | 175篇 |
2022年 | 204篇 |
2021年 | 348篇 |
2020年 | 314篇 |
2019年 | 191篇 |
2018年 | 193篇 |
2017年 | 181篇 |
2016年 | 161篇 |
2015年 | 165篇 |
2014年 | 162篇 |
2013年 | 189篇 |
2012年 | 165篇 |
2011年 | 129篇 |
2010年 | 77篇 |
2009年 | 90篇 |
2008年 | 123篇 |
2007年 | 122篇 |
2006年 | 109篇 |
2005年 | 107篇 |
2004年 | 71篇 |
2003年 | 87篇 |
2002年 | 70篇 |
2001年 | 62篇 |
2000年 | 68篇 |
1999年 | 57篇 |
1998年 | 39篇 |
1997年 | 51篇 |
1996年 | 37篇 |
1995年 | 37篇 |
1994年 | 26篇 |
1993年 | 29篇 |
1992年 | 21篇 |
1991年 | 21篇 |
1990年 | 17篇 |
1989年 | 3篇 |
1988年 | 4篇 |
1986年 | 1篇 |
1985年 | 4篇 |
1984年 | 2篇 |
1983年 | 4篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1979年 | 3篇 |
1974年 | 3篇 |
排序方式: 共有3958条查询结果,搜索用时 15 毫秒
101.
Inside Cover: Lipid Nanotube Tailored Fabrication of Uniquely Shaped Polydopamine Nanofibers as Photothermal Converters (Chem. Eur. J. 13/2016)
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
102.
《Mendeleev Communications》2022,32(3):354-356
The novel conjugates of cholesterol with cobalt – bis(dicarbollide) were synthesized by the ring-opening reactions of the cyclic oxonium derivatives of [3,3′-Co(C2B9H11)2]– with the OH group of cholesterol 2-hydroxyethyl ether. The compounds obtained were tested for toxicity to glioblastoma U-87 MG cells and human embryo fibroblasts FECH-15 cells 相似文献
103.
Dongdong Li Luyao Wang Ernesto Yagüe Linlin Dai Xiumei Zhao Zibo Yang Shuang Zhi Yunhui Hu 《应用有机金属化学》2019,33(10)
An innovative ternary copper(II) complex, [Cu(Cl‐PIP)(Tyr)Cl]n, has been synthesized and characterized using infrared spectroscopy, elemental analysis and single‐crystal X‐ray diffraction analysis. X‐ray crystallography indicates that the Cu atom is five‐coordinated in a square‐pyramidal configuration. The unit forms a one‐dimensional chain along the crystallographic c‐axis. The complex was screened for cytotoxicity against a panel of eight human cancer cell lines, namely MDA‐MB‐231, CAL‐51, K562, HeLa, SGC‐7901, A549, MCF‐7 and SMMC‐7721. The best anticancer activity was obtained with triple‐negative breast cancer CAL‐51 and MDA‐MB‐231 cell lines, with IC50 values in the range 0.035–0.10 μM, and this was better than using carboplatin. The complex inhibits proteasomal chymotrypsin‐like activity, and docking studies reveal its interaction with 20S proteasome. In addition, the complex causes accumulation of ubiquitinated proteins, induces apoptosis and inhibits cell proliferation, indicating its great potential as a novel therapy for triple‐negative breast cancer. 相似文献
104.
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
105.
106.
《中国化学》2017,35(9):1445-1451
Graphene oxide (GO ) and its functionalized derivatives have attracted increasing attention in medical treatment. Herein, a reduction sensitive PEI‐GO ‐SS ‐TPP was synthesized for photodynamic therapy. More than 80% porphyrin release was observed in the presence of 10 mmol•L−1 DTT in one day. The confocal laser scanning microscopy confirmed that the cell uptake efficiency of PEI‐GO‐SS‐TPP was remarkably enhanced as compared to free porphyrin which was significantly dependent on incubation time. For photodynamic therapy, GSH‐OEt could effectively increase the photodynamic therapy efficiency of PEI‐GO ‐SS ‐TPP . Compared with free porphyrin, the toxicity from PEI‐GO ‐SS ‐TPP is much higher with a low IC50 (2.1 µg/mL ) value. All results indicate that the PEI‐GO ‐SS ‐TPP PSs are promising for photodynamic therapy. 相似文献
107.
Dr. Anthony J. Kim Dr. Nicholas J. Boylan Dr. Jung Soo Suk Minyoung Hwangbo Tao Yu Benjamin S. Schuster Dr. Liudimila Cebotaru Dr. Wojciech G. Lesniak Joon Seok Oh Pichet Adstamongkonkul Ashley Y. Choi Prof. Dr. Rangaramanujam M. Kannan Prof. Dr. Justin Hanes 《Angewandte Chemie (International ed. in English)》2013,52(14):3985-3988
108.
109.
Dr. Xiong‐Jie Jiang Dr. Janet T. F. Lau Dr. Qiong Wang Prof. Dennis K. P. Ng Prof. Pui‐Chi Lo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(24):8273-8281
A diiodo distyryl boron dipyrromethene (BODIPY) core was conjugated to two ferrocenyl quenchers through acid‐labile ketal and/or thiol‐cleavable disulfide linkers, of which the fluorescence and photosensitizing properties were significantly quenched through a photoinduced electron‐transfer process. The two symmetrical analogues that contained either the ketal or disulfide linkers could only be activated by a single stimulus, whereas the unsymmetrical analogue was responsive to dual stimuli. Upon interaction with acid and/or dithiothreitol (DTT), these linkers were cleaved selectively. The separation of the BODIPY core and the ferrocenyl moieties restored the photoactivities of the former in phosphate buffered saline and inside the MCF‐7 breast cancer cells, rendering these compounds as potential activable photosensitizers for targeted photodynamic therapy. The dual activable analogue exhibited the greatest enhancement in intracellular fluorescence intensity in both an acidic environment (pH 5) and the presence of DTT (4 mm ). Its photocytotoxicity against MCF‐7 cells also increased by about twofold upon preincubation with 4 mm of DTT. The activation of this compound was also demonstrated in nude mice bearing a HT29 human colorectal carcinoma. A significant increase in fluorescence intensity in the tumor was observed over 9 h after intratumoral injection. 相似文献
110.