全文获取类型
收费全文 | 3552篇 |
免费 | 200篇 |
国内免费 | 267篇 |
专业分类
化学 | 1683篇 |
晶体学 | 41篇 |
力学 | 164篇 |
综合类 | 11篇 |
数学 | 858篇 |
物理学 | 689篇 |
综合类 | 573篇 |
出版年
2024年 | 3篇 |
2023年 | 28篇 |
2022年 | 112篇 |
2021年 | 83篇 |
2020年 | 59篇 |
2019年 | 75篇 |
2018年 | 71篇 |
2017年 | 64篇 |
2016年 | 76篇 |
2015年 | 68篇 |
2014年 | 90篇 |
2013年 | 156篇 |
2012年 | 144篇 |
2011年 | 239篇 |
2010年 | 216篇 |
2009年 | 352篇 |
2008年 | 311篇 |
2007年 | 210篇 |
2006年 | 242篇 |
2005年 | 191篇 |
2004年 | 202篇 |
2003年 | 155篇 |
2002年 | 178篇 |
2001年 | 93篇 |
2000年 | 68篇 |
1999年 | 75篇 |
1998年 | 60篇 |
1997年 | 53篇 |
1996年 | 44篇 |
1995年 | 40篇 |
1994年 | 40篇 |
1993年 | 35篇 |
1992年 | 42篇 |
1991年 | 20篇 |
1990年 | 18篇 |
1989年 | 18篇 |
1988年 | 14篇 |
1987年 | 8篇 |
1986年 | 6篇 |
1985年 | 11篇 |
1984年 | 6篇 |
1983年 | 8篇 |
1981年 | 9篇 |
1980年 | 6篇 |
1979年 | 5篇 |
1978年 | 4篇 |
1977年 | 4篇 |
1976年 | 3篇 |
1974年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有4019条查询结果,搜索用时 15 毫秒
41.
F. I. Zubkov E. V. Nikitina K. F. Turchin A. A. Safronova R. S. Borisov A. V. Varlamov 《Russian Chemical Bulletin》2004,53(4):860-872
The intramolecular Diels—Alder reaction of readily accessible 4-substituted 4-(N-furfuryl)aminobut-1-enes was studied and a new one-step method was developed for the synthesis of 6,8a-epoxy-1,2,3,4,4a,5,6,8a-octahydroisoquinoline (3-aza-11-oxatricyclo[6.2.1.01,6]undec-9-ene) derivatives. The [4+2]-cycloaddition proceeds stereoselectively to form exo-adducts. The influence of substituents at the nitrogen atom in 4-(N-furfuryl)aminobut-1-enes on the cycloaddition pathway was examined. 相似文献
42.
Pentacoordinate complex cations of the general formula [(C6F5)2SbL3]3+ stabilized as solid salts in combination with tetraphenylborate (BPh4), tetrafluorobroate (BF4) anions, where L=DMSO, Ph3AsO, PyO, DMF, α-, β- and γ-picoline have been isolated. The newly formed complexes were characterized by elemental analysis, molar conductance measurements, solid-state IR and and NMR. From these results, a five-fold coordination around antimony was required. 相似文献
43.
Kuno Wagner Kurt Findeisen Walter Schfer Werner Dietrich 《Angewandte Chemie (International ed. in English)》1981,20(10):819-830
Research in the field of low-molecular weight, oligomeric and polymeric α,ω-diisocyanatocarbodiimides and -polycarbodiimides has been fruitful, not only in connection with these compounds themselves, but also—as so often happens in chemistry—with quite different problems. Novel synthetic methods, discoveries concerning the properties of low-molecular weight carbodiimides and phosphane imide derivatives, as well as results on the fragmentation reactions of four-membered heterocyclic compounds containing oxygen, phosphorus, and nitrogen, and a better understanding of the diisocyanate polyaddition process are among the many by-products of this research. The “high- and low-temperature formation” of polycarbodiimides and the homogeneous and heterogeneous catalysis of this process are described, and the fundamental importance of four-membered ring fragmentation mechanisms resulting in the formation of phosphane imide derivatives is outlined. Interesting building blocks for the diisocyanate polyaddition and polycondensation processes can be synthesized by many derivatization reactions of oligomeric and high-molecular weight polycarbodiimides and polyuretonimines. The in situ production of polycarbodiimides via matrix reactions in flexible polyurethane foams leads to a cellular arrangement of the material due to the pronounced symmetrical growth processes. Combination-foams with increased carbonation tendencies are formed in this way. Attention is drawn to several industrial applications of α,ω-diisocyanatopolycarbodiimides, of high-molecular weight cross-linked polyuretonimines, and of polycarbodiimide foams. 相似文献
44.
N. G. Komissarova N. G. Belenkova L. V. Spirikhin O. V. Shitikova M. S. Yunusov 《Chemistry of Natural Compounds》2002,38(1):58-61
Oxidation of betulin by pyridinium dichromate, pyridinium chlorochromate, and K2Cr2O7 -H2SO4 in the presence of tetrabutylammonium bromide was studied. Products of regioselective C-3, C-28-, and exhaustive oxidation, 28-hydroxylup-20(29)-3-one, 3-hydroxy- and 3-oxolup-20(29)-en-28-al were obtained. 相似文献
45.
F. A. L. van der Horst M. H. Post J. J. M. Holthuis U. A. Th. Brinkman 《Chromatographia》1989,28(5-6):267-273
Summary Micellar phase-transfer catalysis (MPTC) offers the opportunity to derivatize carboxylic acids directly in an aqueous matrix without prior extraction of the acids into a suitable aprotic solvent. The currently developed MPTC system consists of a non-ionic surfactant, Arkopal N-130, an ion-pair agent, tetrakis-(decyl)-ammonium bromide, and a novel fluorescence reagent, 9-bromomethylacridine. The MPTC system can be applied to the derivatization of many types of carboxylic acids. The reaction rate is affected by the lipophilicity of the acid and by the presence of other functional groups. For lipophilic carboxylic acids the reaction is complete within 5 min at 60°C and pH 7.0. 相似文献
46.
The organic nanoparticles of a blue-light-emitting molecule, 1,3-diphenyl-5-(9-anthryl)-2-pyrazuline, were prepared by reprecipitation method using acetonitrile as the solvent for the molecular precursor. Three morphologies, spherical, doughnut-shaped and cubic, could be observed on the silicon substrate forthe nanoparfides by the volume-controlled addition of acetonitrile. The evolution of particle morphology as a function of acetonitrile addition was attributed to the variation of the growth habits of the particles in the different environment. The nanoparticles exhibit the novel photoluminescence spectra as compared to those of monomer and the bulk crystals. 相似文献
47.
1 INTRODUCTION During the study of polynuclear complexes with the aim to investigate the magnetic super-exchange interaction between the adjacent metal ions bridged by a conjugation molecule[1], we have made efforts to prepare complexes bridged by 4, 5-diazafluorene-9-one azine (DAA) and found that the coordination ability of DAA is poor in the acidic solution. In order to probe the reason, DAA has been crystallized from the hydrochloric acid solution and its crystal structure has b… 相似文献
48.
研究了第二过渡金属化合物对TiCl4/AleT1.46cL1.54催化丁二烯环化三聚的多金属协同效应。结果表明,极少量的第二过渡金属化合物,如Cr,(acac)3,Mn(acac)3,NiCl2,ZrCl4等加入TiCl4/AlEt1.46Cl1.54体系后不同程度地提高了丁二烯环化三聚的选择性,并改变了体系的最大速率和催化剂效率。 相似文献
49.
Sheng-Lou?DengEmail author Ru-Yu?Chen 《Monatshefte für Chemie / Chemical Monthly》2004,135(9):1113-1119
Summary. A new and simple method for the synthesis of 1,3,2-diazaphosphorines and 1,3,2-oxazaphosphorine was developed based on the reactions of Lawessons reagent with -aminopropionitriles and -hydroxypropionitrile. In addition, a rapid and facile synthesis of 1,3,2-diazaphospholidin-4-ones by the reaction of P(NEt2)3 with hindered diamino substrates under microwave irradiation was also achieved. The prepared phosphorines show herbicidal activity to some extent in the preliminary bioassays. 相似文献
50.
《Electroanalysis》2005,17(2):178-181
Voltammetric behavior of water‐soluble endohedral metallofullerene derivatives Gd@C82(OH)5(NHCH2COOH)9 (GN) and Gd@C82(OH)6(NHCH2CH2SO3H)8 (GS) was characterized in 0.1 M KCl solution by CV and DPV. They showed similar redox behavior, that is, a reversible electroreduction process on HMDE was found; in the mean time, an irreversible oxidation process and an irreversible reduction process on GC electrodes were also observed. The results reveal that these two water‐soluble endohedral metallofullerene derivatives have good electron donating ability and poor electron accepting ability due to hydroxy groups, aminoacetic acid and aminoethyl sulfonic acid connected to the C82 cage in comparison with Gd@C82. 相似文献