全文获取类型
收费全文 | 3309篇 |
免费 | 490篇 |
国内免费 | 163篇 |
专业分类
化学 | 2694篇 |
晶体学 | 29篇 |
力学 | 97篇 |
综合类 | 20篇 |
数学 | 232篇 |
物理学 | 890篇 |
出版年
2024年 | 15篇 |
2023年 | 57篇 |
2022年 | 90篇 |
2021年 | 93篇 |
2020年 | 139篇 |
2019年 | 134篇 |
2018年 | 103篇 |
2017年 | 89篇 |
2016年 | 153篇 |
2015年 | 160篇 |
2014年 | 175篇 |
2013年 | 210篇 |
2012年 | 248篇 |
2011年 | 277篇 |
2010年 | 184篇 |
2009年 | 167篇 |
2008年 | 206篇 |
2007年 | 157篇 |
2006年 | 167篇 |
2005年 | 150篇 |
2004年 | 135篇 |
2003年 | 131篇 |
2002年 | 112篇 |
2001年 | 62篇 |
2000年 | 66篇 |
1999年 | 64篇 |
1998年 | 41篇 |
1997年 | 37篇 |
1996年 | 45篇 |
1995年 | 37篇 |
1994年 | 35篇 |
1993年 | 17篇 |
1992年 | 21篇 |
1991年 | 22篇 |
1990年 | 15篇 |
1989年 | 11篇 |
1988年 | 14篇 |
1987年 | 13篇 |
1986年 | 9篇 |
1985年 | 12篇 |
1984年 | 12篇 |
1983年 | 8篇 |
1982年 | 7篇 |
1981年 | 13篇 |
1980年 | 8篇 |
1979年 | 6篇 |
1977年 | 8篇 |
1976年 | 3篇 |
1974年 | 7篇 |
1973年 | 4篇 |
排序方式: 共有3962条查询结果,搜索用时 15 毫秒
141.
Jian Lin Yitao Li Xiaoyun Hu Weilin Chi Shuiming Zeng Junxing Xu 《Journal of heterocyclic chemistry》2021,58(1):226-240
Very long chain fatty acids (VLCFAs) are one of the most principal and promising targets for herbicides discovery. In order to explore and find novel VLCFAs inhibitors with higher herbicidal activity and improved crop safety, a variety of new 3-{[(5,5-dimethyl-4,5-dihydroisoxazol-3-yl)sulfonyl]methyl}benzo[d]isoxazole derivatives were reasonably designed and synthesized. The results of greenhouse experiments indicated that several compounds exhibited good herbicidal activity against Digitaria sanguinalis, Echinochloa crus-galli, and Setaria faberii at rates of 150 g ai/ha. Compounds g4 and h1 displayed promising herbicidal activity against D sanguinalis and E crus-galli at rates of 75 g ai/ha, which is better than commercial pyroxasulfone and S-metolachlor. Moreover, compound h1 displayed higher activity against E crus-galli, D sanguinalis, and S faberii than pyroxasulfone and S-metolachlor even at a rate of 37.5 and 18.75 g ai/ha. Furthermore, both of the compounds g4 and h1 were much safer to these tested crops, especially to rice, wheat and rape, at the rate of 150 g ai/ha than pyroxasulfone. Therefore, h1 may act as a new lead structure for novel herbicides discovery. 相似文献
142.
143.
Molecular Engineering of Push–Pull Porphyrin Dyes for Highly Efficient Dye‐Sensitized Solar Cells: The Role of Benzene Spacers 下载免费PDF全文
Shaik M. Zakeeruddin Shu‐Nung Chang Chi‐Hung Hsieh Chen‐Yu Yeh Michael Grätzel 《Angewandte Chemie (International ed. in English)》2014,53(11):2973-2977
Porphyrins have drawn much attention as sensitizers owing to the large absorption coefficients of their Soret and Q bands in the visible region. In a donor and acceptor zinc porphyrin we applied a new strategy of introducing 2,1,3‐benzothiadiazole (BTD) as a π‐conjugated linker between the anchoring group and the porphyrin chromophore to broaden the absorption spectra to fill the valley between the Soret and Q bands. With this novel approach, we observed 12.75 % power‐conversion efficiency under simulated one‐sun illumination (AM1.5G, 100 mW cm?2). In this study, we showed the importance of introducing the phenyl group as a spacer between the BTD and the zinc porphyrin in achieving high power‐conversion efficiencies. Time‐resolved fluorescence, transient‐photocurrent‐decay, and transient‐photovoltage‐decay measurements were employed to determine the electron‐injection dynamics and the lifetime of the photogenerated charge carriers. 相似文献
144.
Back Cover: Synthesis,Characterization, Self‐Assembly,Gelation, Morphology and Computational Studies of Alkynylgold(III) Complexes of 2,6‐Bis(benzimidazol‐2′‐yl)pyridine Derivatives (Chem. Eur. J. 32/2014) 下载免费PDF全文
145.
A General Method for Preparing Bridged Organosilanes with Pendant Functional Groups and Functional Mesoporous Organosilicas 下载免费PDF全文
Prof. Jana Hodačová Dr. Guillaume Toquer Dr. Xavier Cattoën Dr. Michel Wong Chi Man 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(33):10371-10382
New organosilica precursors containing two triethoxysilyl groups suitable for the organosilica material formation through the sol‐gel process were designed and synthesised. These precursors display alkyne or azide groups for attaching targeted functional groups by copper‐catalysed azide–alkyne cycloaddition (CuAAC) and can be used for the preparation of functional organosilicas following two strategies: 1) the functional group is first appended by CuAAC under anhydrous conditions, then the functional material is prepared by the sol‐gel process; 2) the precursor is first subjected to the sol‐gel process, producing porous, clickable bridged silsesquioxanes or periodic mesoporous organosilicas (PMOs), then the desired functional groups are attached by means of CuAAC. Herein, we show the feasibility of both approaches. A series of bridged bis(triethoxysilane)s with different pending organic moieties was prepared, demonstrating the compatibility of the first approach with many functional groups. In particular, we demonstrate that organic functional molecules bearing only one derivatisation site can be used to produce bridged organosilanes and bridged silsesquioxanes. In the second approach, clickable PMOs and porous bridged silsesquioxanes were prepared from the alkyne‐ or azide‐containing precursors, and thereafter, functionalised with complementary model azide‐ or alkyne‐containing molecules. These results confirmed the potential of this approach as a general methodology for preparing functional organosilicas with high loadings of functional groups. Both approaches give rise to a wide range of new functional organosilica materials. 相似文献
146.
Dr. Tao Xu Dr. Chi Wai Cheung Prof. Dr. Xile Hu 《Angewandte Chemie (International ed. in English)》2014,53(19):4910-4914
Iron catalysis has been developed for the intermolecular 1,2‐addition of perfluoroalkyl iodides to alkynes and alkenes. The catalysis has a wide substrate scope and high functional‐group tolerance. A variety of perfluoroalkyl iodides including CF3I can be employed. The resulting perfluoroalkylated alkyl and alkenyl iodides can be further functionalized by cross‐coupling reactions. This methodology provides a straightforward and streamlined access to perfluoroalkylated organic molecules. 相似文献
147.
β‐Functionalization of Carboxylic Anhydrides with β‐Alkyl Substituents through Carbene Organocatalysis 下载免费PDF全文
Zhichao Jin Shaojin Chen Yuhuang Wang Pengcheng Zheng Prof. Dr. Song Yang Prof. Dr. Yonggui Robin Chi 《Angewandte Chemie (International ed. in English)》2014,53(49):13506-13509
The first NHC‐catalyzed functionalization of carboxylic anhydrides is described. In this reaction, the β carbon behaves as a nucleophilic carbon and undergoes asymmetric reactions with electrophiles. Anhydrides with challenging β‐alkyl substituents work effectively. 相似文献
148.
Bo Xiao Xiaoyan Chi Li Zhang Huige Qu Yujing Liu Xiaojie Wang Juhua Zhou 《Applied biochemistry and biotechnology》2014,173(8):2129-2139
Efficient expression of target protein is one of strategies for gene therapy or vaccine design. Many studies showed that codon optimization could enhance the expression of target proteins. In this paper, a target sequence of about 1.26 kb encoding the major capsid protein VP6 of grass carp reovirus (GCRV) and an optimized counterpart were synthesized and inserted into vectors for expressing VP6. The final constructs (named as pcDV6G and pcDV6YG) were transfected in Ctenopharyngodon idellus kidney (CIK) cells. The fluorescence analysis and the Western blot results showed that the gene fragment was transfected and expressed in CIK cells successfully. Although the qRT-PCR results showed no difference at the messenger RNA (mRNA) levels between the different versions of vp6 in the indicated stages, the enzyme-linked immunosorbent assay (ELISA) results showed that the protein level of VP6 expressed by pcDV6YG was higher than that by pcDV6G in the indicated hours. Taken together, these results suggest that the enhanced expression of GCRV VP6 in CIK cells by relative sequence optimization may be a good choice for making DNA vaccine against GCRV. 相似文献
149.
Won-Jae Chi Jae-Seon Park Dae-Kyung Kang Soon-Kwang Hong 《Applied biochemistry and biotechnology》2014,173(7):1703-1716
A Gram-negative, aerobic, motile, rod-shaped, agarolytic bacterium, designated as H7, was isolated from a coastal seawater sample. This strain grows at pH 6.0–8.0, temperature of 15–40 °C, and at an NaCl concentration of 1–7 % (w/v). Ubiquinone-8 was the predominant respiratory quinone, and the DNA G+C content was 45.82 mol%. Analysis of the 16S rRNA sequence suggests that strain H7 belongs to the genus Pseudoalteromonas. DNA-DNA hybridization analysis showed DNA relatedness of as low as 55.42 and 40.27 % with its nearest phylogenetic neighbors Pseudoalteromonas atlantica IAM12927T and Pseudoalteromonas espejiana NCIMB2127T, respectively, which led us to name H7 Pseudoalteromonas hodoensis sp. nov. The type strain is H7T (=DSM25967T = KCTC23887T). An agarase (AgaA7) was purified to homogeneity from the cell-free culture broth of H7 through many steps of chromatography. Purified AgaA7 had an apparent molecular weight of 35 kDa, with a distinct NH2-terminal sequence of Ala-Asp-Ala-Thr-X-Pro (X, any amino acid) from the reported proteins, implying that it is a novel enzyme. The optimum pH and temperature for agarase activity were 7.0 and 45 °C, respectively. Thin-layer chromatography analysis, mass spectrometry, and enzyme assay using p-nitrophenyl-α/β-D-galactopyranoside revealed that AgaA7 is both an exo- and endo-type β-agarase that degrades agarose into neoagarotetraose, neoagarohexaose, and neoagarooctaose (minor). 相似文献
150.
Kai Li Xiaolong Tang Honghong Yi Ping Ning Ying Xiang Chi Wang Xianmang Xu 《Research on Chemical Intermediates》2014,40(1):169-177
Manganese–cobalt–cerium oxide (Mn–Co–Ce–Ox) catalysts were synthesized by the co-precipitation method and tested for activity in low-temperature catalytic oxidation of NO in the presence of excess O2. With the best Mn–Co–Ce mixed-oxide catalyst, approximately 80 % NO conversion was achieved at 150 °C and a space velocity of 35,000 h?1. The effect of reaction conditions (reaction temperature, volume fractions of NO and O2, gas hourly space velocity (GHSV), and catalyst stability) was investigated. The optimum reaction temperature was 150 °C. Increasing the O2 content above 3 % results in almost no improvement of NO oxidation. This catalyst enables highly effective removal of NO within a wide range of GHSV. Furthermore, the stability of the Me–Co–Ce–Ox catalyst was excellent; no noticeable decrease of NO conversion was observed in 40 h. 相似文献