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221.
Dr. Velayudham Ramadoss Yue Zheng Xiaoqing Shao Dr. Lifang Tian Prof. Yahui Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(10):3213-3228
Owing to their non-toxic, stable, inexpensive properties, carboxylic acids are considered as environmentally benign alternatives as coupling partners in various organic transformations. Electrochemical mediated decarboxylation of carboxylic acid has emerged as a new and efficient methodology for the construction of carbon-carbon or carbon-heteroatom bonds. Compared with transition-metal catalysis and photoredox catalysis, electro-organic decarboxylative transformations are considered as a green and sustainable protocol due to the absence of chemical oxidants and strong bases. Further, it exhibits good tolerance with various functional groups. In this Minireview, we summarize the recent advances and discoveries on the electrochemical decarboxylative transformations on C−C and C−heteroatoms bond formations. 相似文献
222.
Lu Han Sheng-Jun Li Xue-Ting Zhang Prof. Dr. Shi-Kai Tian 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(9):3091-3097
The charge-accelerated aza-Claisen rearrangement of ammonium salts serves as a key step in the construction of complex nitrogen-containing molecules. However, much less attention has been paid to the aromatic aza-Claisen rearrangement than to the aliphatic one. Herein, we report an unprecedented aromatic aza-Claisen rearrangement of arylpropargylammonium salts, generated in situ from arynes and tertiary propargylamines, delivering structurally diverse 2-propargylanilines in moderate to good yields with high regioselectivity. This rearrangement proceeds in the absence of strong bases or transition metals, is compatible with moisture and air, tolerates a wide variety of functional groups, and is amenable to forming 11- to 13-membered heterocycles with a triple bond. The 2-propargylaniline products were treated with aluminum chloride in ethanol to afford multisubstituted indoles in moderate to excellent yields. Finally, a series of deuterium-labeling experiments was performed to elucidate the reaction mechanism. 相似文献
223.
Yang Min Dr. Chuandong Dou Prof. Hongkun Tian Prof. Jun Liu Prof. Lixiang Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(13):4364-4372
The B←N unit has a large dipole and it is isoelectronic to C−C moiety with no dipole. Incorporating B←N units into π-conjugated system is a powerful strategy to design organic small molecules and polymers with intriguing opto-electronic properties and excellent opto-electronic device performance. However, it is unclear how the B←N unit affects electronic structures and opto-electronic properties of large π-conjugated molecules. In this work, to address this question, we developed three dibenzo-azaacene molecules in which two B←N units were introduced at different positions. Although the dibenzo-azaacene skeleton is fully π-conjugated, the effect of B←N unit on the electronic structures of the adjacent rings is much stronger than that of the distant rings. As a result, the three molecules with isomerized B←N incorporation patterns possess different electronic structures and exhibit tunable opto-electronic properties. Among the three molecules, the centrosymmetrical molecule exhibits higher LUMO/HOMO energy levels than those of the two axisymmetrical molecules. When used as the active layer in organic field-effect transistors (OFETs), while the two axisymmetrical molecules show unipolar electron transporting property, the centrosymmetrical molecule exhibits ambipolar hole and electron transporting behavior. This work not only deepens our understanding on organoboron π-conjugated molecules, but also indicates a new strategy to tune opto-electronic properties of organic semiconductors for excellent device performance. 相似文献
224.
225.
设计了一种输出电压为4 MV的超前触发型Marx发生器,为了进一步优化采用电阻充电的Marx发生器输出特性,提高系统的充电效率并且减小级间充电电压不均匀性,对Marx发生器恒流充电过程进行了解析求解。结果表明:各级间充电电压差为与充电电阻、电容和充电速率成正比,与时间无关的定值,充电时间越长电压效率越高,且与电压变化率无关 。该结论具有普遍适用性。结合我们设计的4 MV超前触发型Marx发生器回路,利用PSpice对Marx发生器的恒流充电过程进行了模拟,得到了自洽的结果,并且与恒压充电进行了对比。当充电电阻为10 k,各级电容为400 nF,充电速率为10 kV/s时,恒流充电能量效率达到90%,约为恒压充电能量效率的2倍,充电时间为恒压充电的1/3。 相似文献
226.
Seed‐Mediated Synthesis of Gold Tetrahedra in High Purity and with Tunable,Well‐Controlled Sizes 下载免费PDF全文
Yiqun Zheng Wenying Liu Tian Lv Ming Luo Dr. Hefei Hu Dr. Ping Lu Dr. Sang‐Il Choi Chao Zhang Dr. Jing Tao Prof. Yimei Zhu Prof. Zhi‐Yuan Li Prof. Younan Xia 《化学:亚洲杂志》2014,9(9):2635-2640
We report a facile synthesis of Au tetrahedra in high purity and with tunable, well‐controlled sizes via seed‐mediated growth. The success of this synthesis relies on the use of single‐crystal, spherical Au nanocrystals as the seeds and manipulation of the reaction kinetics to induce an unsymmetrical growth pattern for the seeds. In particular, the dropwise addition of a precursor solution with a syringe pump, assisted by cetyltrimethylammonium chloride and bromide at appropriate concentrations, was found to be critical to the formation of Au tetrahedra in high purity. Their sizes could be readily tuned in the range of 30–60 nm by simply varying the amount of precursor added to the reaction solution. The current strategy not only enables the synthesis of Au tetrahedra with tunable and controlled sizes but also provides a facile and versatile approach to reducing the symmetry of nanocrystals made of a face‐centered cubic lattice. 相似文献
227.
Mei Tian Huan Huan Sun Xiao Wei Tian Zhi Xin Xu Feng Qiao Wang Dan Shu Yao 《Liquid crystals》2013,40(3):298-308
A series of side-chain liquid crystal (LC) polysiloxanes were synthesised with Poly(methylhydrogeno)siloxane, 4?-(undec-10-enoyloxy) biphenyl – 4 – yl 4- (trifluoromethyl) benzoate (Mth) and a chiral nematic (N*) LC monomer 1-allyl 10-(cholesteryl)-decanedioate (Mch). The chemical structures and LC properties of the monomers and polymers were characterised by FTIR, 1H-NMR, differential scanning calorimetry, thermogravimetric analysis, POM and X-ray diffractometer. Mch is monotropic N* LC. The homopolymer derived from monomer Mch is enantiotropic N* LC. Monomer Mth is a smectic A liquid crystal. The copolymers derived from Mch and Mth are N* LCs. The temperatures at which 5% weight loss occurred are greater than 300°C for all the fluoro-containing polymers, and the residue weights of the samples at 600°C increased slightly as the content of trifluoromethyl mesogens increased in the polymers. The glass transition temperatures of the polymers increased as trifluoromethyl mesogens increased, too. The N*–I phase transition temperatures show a negative deviate from ideal or linear behaviour. The values of the enthalpy changes for the cholesteryl containing polymers are rather low and this is attributed to the biaxiality of cholesteryl moiety which tends to reduce the change in the orientational order at the N*–I transition. Compared to the monomers, the polymers show wider mesophase region. 相似文献
228.
Ji‐Xin Tian Can Peng Lei Xu Yuan Tian Zun‐Jian Zhang 《Biomedical chromatography : BMC》2013,27(6):775-783
In this report, the in vitro metabolism of Strychnos alkaloids was investigated using liquid chromatography/high‐resolution mass spectrometry for the first time. Strychnine and brucine were selected as model compounds to determine the universal biotransformations of the Strychnos alkaloids in rat liver microsomes. The incubation mixtures were separated by a bidentate‐C18 column, and then analyzed by on‐line ion trap/time‐of‐flight mass spectrometry. With the assistance of mass defect filtering technique, full‐scan accurate mass datasets were processed for the discovery of the related metabolites. The structural elucidations of these metabolites were achieved by comparing the changes in accurate molecular masses, calculating chemical component using Formula Predictor software and defining sites of biotransformation based upon accurate MSn spectral information. As a result, 31 metabolites were identified, of which 26 metabolites were reported for the first time. These biotransformations included hydroxylation, N‐oxidation, epoxidation, methylation, dehydrogenation, de‐methoxylation, O‐demethylation, as well as hydrolysis reactions. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
229.
Yanzhen Guo Qian Yang Wei Yan Bing Li Tian Li 《International journal of environmental analytical chemistry》2013,93(10):1001-1012
Acetochlor is an important herbicide for gramineous weeds and some small seed broadleaf weeds. Controlled-release formulations of herbicide are highly desirable not only for attaining the most effective utilisation of the weed control, but also for reducing environmental pollution. Acetochlor was incorporated in poly (butyl methacrylate-diacetone acrylamide) based formulation to obtain controlled release properties. The acetochlor nanocapsules were characterised by size distribution, infrared spectroscopy (IR) and field emission scanning electron microscopy (FESEM), and factors related to loading efficiency, swelling behaviour of the formulation were investigated. For this controlled-release formulation, the loading efficiency could reach about 50% (w/w). n, the diffusion parameter was indicative of the transport mechanism, and the values for ‘n’ were in the range of 0.28–0.61, which indicated that the release of acetochlor was diffusion-controlled. The time taken for 50% of the active ingredient to be released into water, t50, was also calculated for the comparison of formulations in different conditions. The formulation with higher temperature and more diacetone acrylamide had lower value of t50, which means a quicker release of the active ingredient. This study highlighted some pieces of evidence that improved herbicide incorporation and slower release were linked to potential interactions between the herbicide and the polymer. 相似文献
230.
A new metal complex[MnL2](NO3)2·CH3CN(1) was synthesized by reaction of 4’-4-(l,2,4-triazol-l-yl)phenyl -2,2’:6’,2"-terpyridine(L) with manganese nitrate.The structure of the complex was determined by X-ray crystallography.The results of UV-vis studies showed that the complex exhibits colorimetric sensing ability for Fe3+,which can be observed by naked eye. 相似文献