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31.
La2Zr2O7(LZO)过渡层以其独特的物理化学性质越来越受到人们的关注。本文以乙酰丙酮镧和乙酰丙酮锆为前驱盐,丙酸为溶剂配置前驱液,用化学溶液方法(CSD)在具有立方织构的Ni-5at%W基底上制备了LZO过渡层薄膜。研究了前驱液成分、性质以及退火温度对LZO成相以及取向的影响。用常规XRD和X射线四环衍射仪分析了LZO薄膜的相成分和织构。结果显示,在1050℃下退火可以获得强立方织构的LZO薄膜,其中(222)峰的Phi扫描半高宽值为8.95°;(400)峰的Chi扫描半高宽值为6.8°。用高分辨扫描电子显微镜(FE-SEM)观察到LZO薄膜表面均匀致密,没有裂纹和空洞。 相似文献
32.
Xiaohui Duan Mina Zhang Huan Du Xiu Gu Caihong Bai Liuqiang Zhang Kaixian Chen Kaifeng Hu Yiming Li 《Molecules (Basel, Switzerland)》2022,27(15)
Scrophulariae Radix (SR) is one of the oldest and most frequently used Chinese herbs for oriental medicine in China. Before clinical use, the SR should be processed using different methods after harvest, such as steaming, “sweating”, and traditional fire-drying. In order to investigate the difference in chemical constituents using different processing methods, the two-dimensional (2D) 1H-13C heteronuclear single quantum correlation (1H-13C HSQC)-based metabolomics approach was applied to extensively characterize the difference in the chemical components in the extracts of SR processed using different processing methods. In total, 20 compounds were identified as potential chemical markers that changed significantly with different steaming durations. Seven compounds can be used as potential chemical markers to differentiate processing by sweating, hot-air drying, and steaming for 4 h. These findings could elucidate the change of chemical constituents of the processed SR and provide a guide for the processing. In addition, our protocol may represent a general approach to characterizing chemical compounds of traditional Chinese medicine (TCM) and therefore might be considered as a promising approach to exploring the scientific basis of traditional processing of TCM. 相似文献
33.
Jos L. Medina-Franco Edgar Lpez-Lpez Liliam P. Martínez-Fernndez 《Molecules (Basel, Switzerland)》2022,27(9)
Inhibitors of epigenetic writers such as DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug and probe discovery. To advance epigenetic probes and drug discovery, chemical companies are developing focused libraries for epigenetic targets. Based on a knowledge-based approach, herein we report the identification of two quinazoline-based derivatives identified in focused libraries with sub-micromolar inhibition of DNMT1 (30 and 81 nM), more potent than S-adenosylhomocysteine. Also, both compounds had a low micromolar affinity of DNMT3A and did not inhibit DNMT3B. The enzymatic inhibitory activity of DNMT1 and DNMT3A was rationalized with molecular modeling. The quinazolines reported in this work are known to have low cell toxicity and be potent inhibitors of the epigenetic target G9a. Therefore, the quinazoline-based compounds presented are attractive not only as novel potent inhibitors of DNMTs but also as dual and selective epigenetic agents targeting two families of epigenetic writers. 相似文献
34.
Vasily A. Kezin Elena S. Matyugina Mikhail S. Novikov Alexander O. Chizhov Robert Snoeck Graciela Andrei Sergei N. Kochetkov Anastasia L. Khandazhinskaya 《Molecules (Basel, Switzerland)》2022,27(9)
Pyrimidine nucleoside analogues are widely used to treat infections caused by the human immunodeficiency virus (HIV) and DNA viruses from the herpes family. It has been shown that 5-substituted uracil derivatives can inhibit HIV-1, herpes family viruses, mycobacteria and other pathogens through various mechanisms. Among the 5-substituted pyrimidine nucleosides, there are not only the classical nucleoside inhibitors of the herpes family viruses, 2′-deoxy-5-iodocytidine and 5-bromovinyl-2′-deoxyuridine, but also derivatives of 1-(benzyl)-5-(phenylamino)uracil, which proved to be non-nucleoside inhibitors of HIV-1 and EBV. It made this modification of nucleoside analogues very promising in connection with the emergence of new viruses and the crisis of drug resistance when the task of creating effective antiviral agents of new types that act on other targets or exhibit activity by other mechanisms is very urgent. In this paper, we present the design, synthesis and primary screening of the biological activity of new nucleoside analogues, namely, 5′-norcarbocyclic derivatives of substituted 5-arylamino- and 5-aryloxyuracils, against RNA viruses. 相似文献
35.
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37.
《Analytical letters》2012,45(14):1185-1189
Abstract A specific and non-destructive test for basic esters of benzilic and α-glycolic acids in water is described. The compounds are collected on a glass fiber filter as water insoluble complexes with sodium tetraphenylboron. The filter is dried and sprayed with a 2-diphenylacetyl-l, 3-indandione-l-imine derivative. A positive test is the visual observation of fluorescence. 相似文献
38.
An incremental algorithm may yield an enormous computational time saving to solve a network flow problem. It updates the solution to an instance of a problem for a unit change in the input. In this paper we have proposed an efficient incremental implementation of maximum flow problem after inserting an edge in the network G. The algorithm has the time complexity of O((n)2
m), where n is the number of affected vertices and m is the number of edges in the network. We have also discussed the incremental algorithm for deletion of an edge in the network G. 相似文献
39.
The vector partition problem concerns the partitioning of a set A of n vectors in d-space into p parts so as to maximize an objective function c which is convex on the sum of vectors in each part. Here all parameters d, p, n are considered variables. In this paper, we study the adjacency of vertices in the associated partition polytopes. Using our adjacency characterization for these polytopes, we are able to develop an adaptive algorithm for the vector partition problem that runs in time O(q(L)v) and in space O(L), where q is a polynomial function, L is the input size and v is the number of vertices of the associated partition polytope. It is based on an output-sensitive algorithm for enumerating all vertices of the partition polytope. Our adjacency characterization also implies a polynomial upper bound on the combinatorial diameter of partition polytopes. We also establish a partition polytope analogue of the lower bound theorem, indicating that the output-sensitive enumeration algorithm can be far superior to previously known algorithms that run in time polynomial in the size of the worst-case output. 相似文献
40.