全文获取类型
收费全文 | 15765篇 |
免费 | 2749篇 |
国内免费 | 2185篇 |
专业分类
化学 | 11432篇 |
晶体学 | 285篇 |
力学 | 1005篇 |
综合类 | 174篇 |
数学 | 1550篇 |
物理学 | 6253篇 |
出版年
2024年 | 19篇 |
2023年 | 283篇 |
2022年 | 391篇 |
2021年 | 566篇 |
2020年 | 735篇 |
2019年 | 657篇 |
2018年 | 597篇 |
2017年 | 548篇 |
2016年 | 801篇 |
2015年 | 837篇 |
2014年 | 1096篇 |
2013年 | 1280篇 |
2012年 | 1351篇 |
2011年 | 1462篇 |
2010年 | 1084篇 |
2009年 | 947篇 |
2008年 | 1157篇 |
2007年 | 1041篇 |
2006年 | 924篇 |
2005年 | 750篇 |
2004年 | 551篇 |
2003年 | 483篇 |
2002年 | 429篇 |
2001年 | 371篇 |
2000年 | 318篇 |
1999年 | 280篇 |
1998年 | 210篇 |
1997年 | 211篇 |
1996年 | 222篇 |
1995年 | 163篇 |
1994年 | 138篇 |
1993年 | 127篇 |
1992年 | 96篇 |
1991年 | 89篇 |
1990年 | 89篇 |
1989年 | 59篇 |
1988年 | 58篇 |
1987年 | 47篇 |
1986年 | 42篇 |
1985年 | 35篇 |
1984年 | 26篇 |
1983年 | 18篇 |
1982年 | 20篇 |
1981年 | 15篇 |
1980年 | 11篇 |
1979年 | 8篇 |
1975年 | 5篇 |
1974年 | 5篇 |
1970年 | 12篇 |
1937年 | 5篇 |
排序方式: 共有10000条查询结果,搜索用时 297 毫秒
981.
Dr. Yongxin Li Pan Sun Luyang Zhao Prof. Xuehai Yan Prof. Dennis K. P. Ng Prof. Pui-Chi Lo 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(51):23428-23438
A facile approach to assemble catalase-like photosensitizing nanozymes with a self-oxygen-supplying ability was developed. The process involved Fe3+-driven self-assembly of fluorenylmethyloxycarbonyl (Fmoc)-protected amino acids. By adding a zinc(II) phthalocyanine-based photosensitizer (ZnPc) and the hypoxia-inducible factor 1 (HIF-1) inhibitor acriflavine (ACF) during the Fe3+-promoted self-assembly of Fmoc-protected cysteine (Fmoc-Cys), the nanovesicles Fmoc-Cys/Fe@Pc and Fmoc-Cys/Fe@Pc/ACF were prepared, which could be disassembled intracellularly. The released Fe3+ could catalyze the transformation of H2O2 enriched in cancer cells to oxygen efficiently, thereby ameliorating the hypoxic condition and promoting the photosensitizing activity of the released ZnPc. With an additional therapeutic component, Fmoc-Cys/Fe@Pc/ACF exhibited higher in vitro and in vivo photodynamic activities than Fmoc-Cys/Fe@Pc, demonstrating the synergistic effect of ZnPc and ACF. 相似文献
982.
Fei Du Shi-Jun Li Kun Jiang Rong Zeng Prof. Xi-Chun Pan Prof. Dr. Yu Lan Prof. Dr. Ying-Chun Chen Prof. Dr. Ye Wei 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(52):23963-23970
We have rationally designed a new class of alkyne-tethered oximes and applied them in an unprecedented iron-catalyzed radical relay protocol for the rapid assembly of a wide array of structurally new and interesting fused pyridines. This method shows broad substrate scope and good functional-group tolerance and enabled the synthesis of several biologically active molecules. Furthermore, the fused pyridines could be diversely functionalized through various simple transformations, such as cyclization, C−H alkylation, and a click reaction. DFT calculation studies indicate that the reactions involve cascade 1,5-hydrogen atom transfer, 5-exo-dig radical addition, and cyclization processes. Moreover, preliminary biological investigations suggest that some of the fused pyridines exhibit good anti-inflammatory activity by restoring the imbalance of inflammatory homeostasis of macrophages in a lipopolysaccharide-induced model. 相似文献
983.
984.
985.
Jinwei Sun Xinrui Yang Yun Liu Yi Wang Yi Pan 《Journal of heterocyclic chemistry》2020,57(3):1449-1455
An efficient synthesis of 3-nitroimidazo[1,2-a]pyridines has been developed via N-iodosuccinimide (NIS)-mediated multicomponents reaction of 2-aminopyridines, aldehydes, and nitromethane under metal-free conditions. This protocol has many advantages such as broad substituent scope, mild and eco-friendly conditions, high step economy, and good yields. 相似文献
986.
Wan-Chen Pan Yi-Chun Wang Tuan-Jie Li Jian-Quan Liu Xiang-Shan Wang 《Journal of heterocyclic chemistry》2020,57(11):3970-3979
Aldehyde could undergo not only the subsequent condensation and cyclization with 2-aminothiophene-3-carboxamide to build a pyrimidine ring, but also a Friedel-Crafts alkylation reaction with thiophene moiety to give unexpected 6-benzyl-2-arylthieno[2,3-d]pyrimidin-4(3H)- ones in good yields catalyzed by concentrated HCl. 相似文献
987.
Dr. Jinqiao Dong Yutong Pan Dr. Heng Wang Dr. Kuiwei Yang Dr. Lingmei Liu Prof. Zhiwei Qiao Yi Di Yuan Shing Bo Peh Dr. Jian Zhang Dr. Leilei Shi Prof. Hong Liang Prof. Yu Han Prof. Xiaopeng Li Prof. Jianwen Jiang Prof. Bin Liu Prof. Dan Zhao 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(25):10237-10245
The self-assembly of highly stable zirconium(IV)-based coordination cages with aggregation induced emission (AIE) molecular rotors for in vitro bio-imaging is reported. The two coordination cages, NUS-100 and NUS-101, are assembled from the highly stable trinuclear zirconium vertices and two flexible carboxyl-decorated tetraphenylethylene (TPE) spacers. Extensive experimental and theoretical results show that the emissive intensity of the coordination cages can be controlled by restricting the dynamics of AIE-active molecular rotors though multiple external stimuli. Because the two coordination cages have excellent chemical stability in aqueous solutions (pH stability: 2–10) and impressive AIE characteristics contributed by the molecular rotors, they can be employed as novel biological fluorescent probes for in vitro live-cell imaging. 相似文献
988.
Wu Wen Shengsheng Yu Chaoqun Zhou Prof. Hao Ma Prof. Zhongyue Zhou Chuangchuang Cao Dr. Jiuzhong Yang Minggao Xu Prof. Fei Qi Prof. Guobin Zhang Prof. Yang Pan 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(12):4903-4908
HCHO has been confirmed as an active intermediate in the methanol-to-hydrocarbon (MTH) reaction, and is critical for interpreting the mechanisms of coke formation. Here, HCHO was detected and quantified during the MTH process over HSAPO-34 and HZSM-5 by in situ synchrotron radiation photoionization mass spectrometry. Compared with conventional methods, excellent time-resolved profiles were obtained to study the formation and fate of HCHO, and other products during the induction, steady-state reaction, and deactivation periods. Similar formation trends of HCHO and methane, and their close correlation in yields suggest that they are derived from disproportionation of methanol at acidic sites. In the presence of Y2O3, the amount of HCHO changes, affecting the hydrogen-transfer processes of olefins into aromatics and aromatics into cokes. The yield of HCHO affects the aromatic-based cycle and the formation of ethylene, indicating that ethylene is mainly formed from the aromatic-based cycle. 相似文献
989.
Abeer F. Shunnar Dr. Bhausaheb Dhokale Dr. Durga Prasad Karothu David H. Bowskill Dr. Isaac J. Sugden Dr. Hector H. Hernandez Prof. Panče Naumov Dr. Sharmarke Mohamed 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(21):4752-4765
The discovery of molecular ionic cocrystals (ICCs) of active pharmaceutical ingredients (APIs) widens the opportunities for optimizing the physicochemical properties of APIs whilst facilitating the delivery of multiple therapeutic agents. However, ICCs are often observed serendipitously in crystallization screens and the factors dictating their crystallization are poorly understood. We demonstrate here that mechanochemical ball milling is a versatile technique for the reproducible synthesis of ternary molecular ICCs in less than 30 min of grinding with or without solvent. Computational crystal structure prediction (CSP) calculations have been performed on ternary molecular ICCs for the first time and the observed crystal structures of all the ICCs were correctly predicted. Periodic dispersion-corrected DFT calculations revealed that all the ICCs are thermodynamically stable (mean stabilization energy=−2 kJ mol−1) relative to the crystallization of a physical mixture of the binary salt and acid. The results suggest that a combined mechanosynthesis and CSP approach could be used to target the synthesis of higher-order molecular ICCs with functional properties. 相似文献
990.
Guohai Deng Shujun Lei Dr. Sudip Pan Jiaye Jin Prof. Guanjun Wang Prof. Lili Zhao Prof. Mingfei Zhou Prof. Gernot Frenking 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(46):10487-10500
Homoleptic Group 4 metal carbonyl cation and neutral complexes were prepared in the gas phase and/or in solid neon matrix. Infrared spectroscopy studies reveal that both zirconium and hafnium form eight-coordinate carbonyl neutral and cation complexes. In contrast, titanium forms only the six-coordinate Ti(CO)6+ and seven-coordinate Ti(CO)7. Titanium octacarbonyl Ti(CO)8 is unstable as a result of steric repulsion between the CO ligands. The 20-electron Zr(CO)8 and Hf(CO)8 complexes represent the first experimentally observed homoleptic octacarbonyl neutral complexes of transition metals. The molecules still fulfill the 18-electron rule, because one doubly occupied valence orbital does not mix with any of the metal valence atomic orbitals. Zr(CO)8 and Hf(CO)8 are stable against the loss of one CO because the CO ligands encounter less steric repulsion than Zr(CO)7 and Hf(CO)7. The heptacarbonyl complexes have shorter metal−CO bonds than that of the octacarbonyl complexes due to stronger electrostatic and covalent bonding, but the significantly smaller repulsive Pauli term makes the octacarbonyl complexes stable. 相似文献