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991.
Zhi‐Yong Jiang Le‐Yu Zhu Jun Zhou Qiu‐Fen Hu Guang‐Yu Yang Xiang‐Zhong Huang Wen‐Xing Liu Lu Gao Gan‐Peng Li Fu‐Ting Xia 《Helvetica chimica acta》2016,99(6):452-456
A novel terpenoid, named perovskiaol ( 1 ), was isolated from the cultured Perovskia atriplicifolia. Its structure was elucidated by comprehensive spectroscopic analysis as well as by quantum chemical computation of electronic circular dichroism spectra. Perovskiaol ( 1 ) was a novel C22 terpenoid containing a unique D‐ring simultaneously fused with rings A, B, and C, and encountered in nature for the first time. Cytotoxic bioassay suggested perovskiaol ( 1 ) possessed significant cytotoxic activity inhibiting NB4, A549, and HepG 2 cell lines with IC50 values of 2.35, 1.47, and 0.81 μm , respectively. 相似文献
992.
A new C‐glycosyl flavone containing a 3‐keto sugar, isocassiaoccidentalin B ( 1 ), was isolated from whole Cassia nomame (Sieber ) Honda plants, along with eleven known compounds, including two flavonoids ( 2 and 3 ), five flavonoid glycosides ( 4 – 8 ), two chalcones ( 9 and 10 ), and two phenylpropanoids ( 11 and 12 ). The chemical structures of all compounds were determined via 1D‐ and 2D‐NMR, and ESI‐MS. Among these, compounds 2 , 3 , 7 , and 8 were found to be the most potent in inhibiting nitric oxide release. Compounds 1 , 2 , 4 , 8 , 9 , and 10 showed significant free‐radical scavenging activity. 相似文献
993.
Electrochemical Investigations of Mn and Al Co‐doped Li2FeSiO4/C Cathodes for Li‐Ion Battery 下载免费PDF全文
Few studies on orthosilicate cathodes co‐doped with two cations have been reported until now. Here, we report the synthesis of Mn and Al co‐doped Li2Fe0.8?xMn0.2AlxSiO4 (x = 0.05 and 0.1) by a solid‐state reaction route and characterized by X‐ray diffraction (XRD), particle size analysis, scanning electron microscopy (SEM), galvanostatic charge/discharge tests, and capacity intermittent titration technique (CITT), as compared to the single‐doped Li2Fe0.8Mn0.2SiO4. Though the co‐doping leads to a slight decreased capacity owing to the increased impurity and Al3+ inertia, a better cycling performance is obtained as expected. Especially when x is 0.05, the modified sample (Li2Fe0.75Mn0.2Al0.05SiO4) shows an initial discharge capacity of 159.3 mAh/g and high capacity retention of 78% after 50 charge/discharge cycles. The present work indicates that a synergistic effect of Mn and Al co‐substitution at the Fe site could partly make up the disadvantage of single Mn doping, and might provide an effective guide for the dopant incorporation to Li2FeSiO4 systems. 相似文献
994.
Environment‐sensitive Fluorescent Turn‐on Chemical Probe for the Specific Detection of O‐Methylguanine‐DNA Methyltransferase (MGMT) in Living Cells 下载免费PDF全文
MGMT protein, which has been associated with resistance to antitumor alkylation drugs for many patients, is a very useful prognostic marker to provide a guide for therapeutic decisions. Considering the large number of cellular samples that have to be handled daily at the hospitals, it is thus important to develop a rapid and simple analytical method to distinguish MGMT activity in different types of cells. In this paper, we describe a MGMT‐activated fluorescence turn‐on probe for the rapid no‐wash imaging of MGMT in living cells. The probe consists of a specific MGMT suicide pseudosubstrate, O6‐benzyl‐guanine and an environment‐sensitive fluorophore, SBD. In the presence of MGMT, the enzyme transfers SBD to the protein active site where the hydrophobic surrounding causes the fluorophore to exhibit more than 50‐fold fluorescence enhancement. With this probe, bright fluorescence was observed for MGMT‐positive, Hela S3 and MCF‐7 cells, while MGMT‐deficient CHO cells displayed no fluorescence. We believe that this fluorescence activation probe design can also be extended to detect other transferases, for which there are still no effective methods to image them in living cells. 相似文献
995.
Synthesis and Characterization of Copper(II)–Phosphonate Coordination Chain Array of Metallocages 下载免费PDF全文
Reaction of CuCl2 ·2H2O and 2,4,6‐tris(phosphorylmethyl)mesitylene (H6tpmm) in H2O?DMF solution at room temperature afforded green crystals of [Cu6(H2tpmm)3(H2O)9]·3H2O ( 1 ), which were characterized by Fourier transform infrared (FT‐IR), thermogravimetric (TG) analysis, and powder X‐ray diffraction (PXRD). The solid‐state structure of 1 reveals a one‐dimensional chain array of M4L2 ‐metallocages constituted by the connection of two kinds of metallocage units, namely MC‐A (phosphonate/water‐bridged) and MC‐B (phosphonate‐bridged only), via μ2‐O(phosphonate)? Cu bonds in ABAABA order. The tris‐phosphonate ligand H6tpmm is partially deprotonated to form H2tpmm4?, which displays a cis,cis,cis conformation to bridge six Cu(II) centers via two monodentate phosphonate groups in a η 0:η 0:η 1‐bonding mode and one tridentate phosphonate group in a μ4, η 1:η 1:η 2‐bondingng mode. 相似文献
996.
Synthesis and Antiviral Bioactivity of Novel 2‐Substituted Methlthio‐5‐(4‐Amino‐2‐Methylpyrimidin‐5‐yl)‐1,3,4‐Thiadiazole Derivatives 下载免费PDF全文
Wen‐Neng Wu An‐Qi Tai Qin Chen Gui‐Ping Ouyang 《Journal of heterocyclic chemistry》2016,53(2):626-632
A series of novel 2‐substituted methlthio‐5‐(4‐amino‐2‐methylpyrimidin‐5‐yl‐)‐1,3,4‐thiadiazole derivatives were synthesized, characterized and evaluated for antiviral activities against tobacco mosaic virus (TMV). The preliminary biological results indicated that most compounds exhibit excellent antiviral activity against TMV in vivo. Among these compounds, compounds 9c , 9i , and 9p displayed the similar curative effect against TMV (EC50 = 287.05–322.47 µg/mL) to that of the commercial agent Ningnanmycin (EC50 = 301.83 µg/mL). In particular, compound 9d demonstrated the best curative effect against TMV (EC50 = 266.21 µg/mL), which was better than that of commercial Ningnanmycin. 相似文献
997.
Green Synthesis of Spiro[indoline‐3,4′‐pyrazolo[3,4‐b][1,6]naphthyridine]‐2,5′(1′H)‐diones Catalyzed by TsOH in Ionic Liquids 下载免费PDF全文
Bin‐Bin Feng Rong‐Zhang Jin Mei‐Mei Zhang Xiang‐Shan Wang 《Journal of heterocyclic chemistry》2016,53(5):1578-1583
A three‐component reaction of isatin, 3‐methyl‐1‐phenyl‐1H‐pyrazol‐5‐amine, and piperidine‐2,4‐dione was treated in ionic liquids catalyzed by TsOH and provided an efficient and green method for the synthesis of spiro[indoline‐3,4′‐pyrazolo[3, 4‐b][1,6]naphthyridine]‐2,5′(1′H)‐dione derivatives in high yields. 相似文献
998.
N. A. A. Elkanzi Ashraf A. Aly Ahmed M. Shawky Essmat M. El‐Sheref Nesrin M. Morsy Ahmed A. M. El‐Reedy 《Journal of heterocyclic chemistry》2016,53(6):1941-1944
Reactions of amidines with malononitrile dimer in DMF and catalyzed with piperidine are reported. The reaction occurred via amination process followed by cyclization to give racemic 6‐aminopyrimidine compounds. The reaction mechanism was discussed. The structure of products was elucidated by mass spectrometry, IR and NMR spectra together with elemental analyses. 相似文献
999.
Wen‐Neng Wu Man‐Ni Gao Hong Tu Gui‐Ping Ouyang 《Journal of heterocyclic chemistry》2016,53(6):2042-2048
A series of novel N‐substituted‐2‐(6‐morpholino‐9H‐purin‐9‐yl)acetamide and 4‐(9‐((5‐substituted‐1,3,4‐oxadiazole/thiadiazole‐2‐yl)methyl)‐9H‐purin‐6‐yl)‐morpholine derivatives were synthesized and evaluated their antibacterial activities against rice bacterial leaf blight and tobacco bacterial wilt caused by Xanthomonas oryzae pv. oryzae (Xoo) and Ralstonia solanacearum (R. solanacearum) via the turbidimeter test in vitro. Antibacterial bioassay indicated that most compounds demonstrated good inhibitory effect against Xoo and R. solanacearum. Especially, compound 6a demonstrated the best inhibitory effect against Xoo with half‐maximal effective concentration (EC50) value of 8.39 μg/mL, which was even better than those of commercial agents Bismerthiazol and Thiodiazole copper. The synthesized purine derivatives containing amide and 1,3,4‐oxadiazole/thiadiazole moieties exhibited excellent antibacterial activities against Xanthomonas oryzae pv. oryzae and R. solanacearum in vitro. 相似文献
1000.
Ortho‐hydroxyl effect and proton transfer via ion–neutral complex: the fragmentation study of protonated imine resveratrol analogues in mass spectrometry 下载免费PDF全文
Lei Yue Jing Li Xiaodong Xie Cheng Guo Xinchi Yin Qi Yin Yinjuan Chen Yuanjiang Pan Chuanfan Ding 《Journal of mass spectrometry : JMS》2016,51(7):518-523
The fragmentation pathways of protonated imine resveratrol analogues in the gas‐phase were investigated by electrospray ionization–tandem mass spectrometry. Benzyl cations were formed in the imine resveratrol analogues that had an ortho‐hydroxyl group on the benzene ring A. The specific elimination of the quinomethane neutral, CH2 = C6H4 = O, from the two isomeric ions [M1 + H]+ and [M3 + H]+ via the corresponding ion–neutral complexes was observed. The fragmentation pathway for the related meta‐isomer, ion [M2 + H]+ and the other congeners was not observed. Accurate mass measurements and additional experiments carried out with a chlorinated analogue and the trideuterated isotopolog of M1 supported the overall interpretation of the fragmentation phenomena observed. It is very helpful for understanding the intriguing roles of ortho‐hydroxyl effect and ion–neutral complexes in fragmentation reactions and enriching the knowledge of the gas‐phase chemistry of the benzyl cation. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献