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排序方式: 共有795条查询结果,搜索用时 15 毫秒
1.
Christopher J. Nichols 《Tetrahedron letters》2004,45(40):7469-7473
A number of new functionalised bridged indolocarbazole systems have been prepared by ring-opening reactions of a key cyclic sulfate intermediate, prepared from the corresponding diol by the action of sulfuryl diimidazole and DBU. The same cyclic sulfate also undergoes an unprecedented asymmetric rearrangement to a chiral ketone, on treatment with a chiral lithium amide base. 相似文献
2.
Jean-Marcel Colmont François Rohart Jean-Pierre Bouanich 《Journal of Molecular Spectroscopy》2006,238(1):98-107
Extensive experiments on the K = 3 component of the J = 12-11 rotational transition of acetonitrile CH3C14N, located near 220.7 GHz, were performed at different temperatures in the range 235-350 K. They allow determining the N2-, H2-, and He-broadening coefficients, as well as their temperature dependences. More specific measurements on all the K-components of the involved transition perturbed by N2 at 303 K allow to point out a clear decreasing of the broadening coefficient with increasing K. Narrowing effects are clearly observed, and experimental lines were analysed both with Voigt and speed dependent Voigt profiles; but no exhaustive lineshape study was carried out. All the experimental parameters are compared with results derived from a semiclassical calculation of collisional interactions, including electrostatic, induction, and dispersion energy contributions. 相似文献
3.
Bikshandarkoil R. Srinivasan 《Journal of Chemical Sciences》2004,116(5):251-259
The complexes [MoX4]2− (M = Mo; X = O or S) exist as the monomeric tetrahedral species in aqueous alkaline solutions. Acidification of tetraoxomolybdate
results in the condensation of the tetrahedral units via a series of polyoxomolybdates leading to the ultimate formation of
the trioxide MoO3. Heptamolybdate [Mo7O24]6− is the first major polyanion of the acidification reaction. In contrast, acidification of tetrathiomolybdates leads to the
formation of amorphous molybdenum trisulphide via a dinuclear Mo(V) complex. The formation of the dinuclear Mo(V) complex
precludes the formation of any higher nuclearity Mo(VI)-S complexes in aqueous solution. Thus it is shown that the all-sulphur
analogue of heptamolybdate [M07S24]6− does not exist in alkaline medium and also cannot be isolated from aqueous acidic medium 相似文献
4.
The fourth-order ordinary differential equation that defines the self-similar solutions of the Kaup—Kupershmidt and Sawada—Kotera
equations is studied. This equation belongs to the class of fourth-order analogues of the Painlevé equations. All the power
and non-power asymptotic forms and expansions near points z = 0, z = ∞ and near an arbitrary point z = z
0 are found by means of power geometry methods. The exponential additions to the solutions of the studied equation are also
determined.
相似文献
5.
以氯化锌、铁氰化钾(含有整合剂)的水溶液为原料,合成了铁锌双金属氰化物(DMC)催化剂。为获得高活性的DMC催化剂,需将叔丁醇 、多元醇螯合剂螯合至其结构中,用XRD、XPS等分析手段,对铁锌DMC催化剂的结构与活性进行分析表征。实验发现,DMC催化剂的晶体结构与螯合剂密切相关,螯合剂能显著降低DMC催化剂的结晶程度,从而提高DMC催化剂的活性。同时,氯化锌过量也有利于DMC催化剂活性的提高。并表征了相关DMC催化剂的活性中心。 相似文献
6.
4-Amino-3-hydroxybutyric acid was synthesized from allyl cyanide in four steps in an overall yield of 38%. Ultrasonically promoted epoxidation of allyl cyanide with m-chloroperoxybenzoic acid giving oxiranylacetonitrile was used as a key step. 相似文献
7.
Francisco García-Montelongo María J. Sánchez Miguel A. Rodríguez 《Mikrochimica acta》1989,98(4-6):259-265
A spectrophotometric method for cyanide based on its inhibition of the colour formation reaction between nickel(II) and 3-(4,5-dimethyl-2-thiazolylazo)-2,6-dihydroxybenzoic acid has been developed, and allows the determination of down to 0.1 g of cyanide. Most of the interferences can be avoided by displacement of the hydrogen cyanide using an arsine generator. 相似文献
8.
本文综述了前列环素及其类似物的合成。类似物包括有7-羰基—、10,10-二氟—、5-氯—,4-羰基—、6,9-硫—、6,9-氮—,6 a-碳—前列环素以及苯前列环素等。前列环素及其类似物是一类具有抑制血小板聚集的生物活性化合物。 相似文献
9.
Hiratake J 《Chemical record (New York, N.Y.)》2005,5(4):209-228
Carefully designed molecules that are intimately related to the reaction mechanism of enzymes are often highly selective and potent inhibitors that serve as extremely useful chemical probes for understanding the reaction mechanism and structure of enzymes. This article describes the design, synthesis, and applications of specific inhibitors of two mechanistically distinct groups of enzymes, ATP-dependent amide ligases and Ser- and Thr-hydrolases. Our strategy is based on the premise that stable analogues of the transition state (transition-state analogues) are highly potent inhibitors that serve as good mechanistic probes, and that a key structure of a good inhibitor of one enzyme is also utilized for the inhibitors of other enzymes that share the same chemistry in their catalyzed reactions, irrespective of the degree of structural similarity and evolutionary link between the enzymes. According to these principles, we designed and synthesized a series of phosphinate- and sulfoximine-based transition-state analogue inhibitors of glutathione synthetase, gamma-glutamylcysteine synthetase and asparagine synthetase. For the second group of enzymes, we synthesized a gamma-monofluorophosphono glutamate analogue for mechanism-based affinity labeling of gamma-glutamyltranspeptidase and fluorescent phosphonic acid esters for the active-site titration of lipase. These inhibitors were used successfully as ligands for detailed kinetic analyses, X-ray crystallography, and mass analysis of the enzymes to identify the key amino acid residues responsible for catalysis and substrate recognition in the transition state. 相似文献
10.
双金属氰化物络合物催化环氧烷烃开环聚合的特征 总被引:9,自引:0,他引:9
合成了Co Zn双金属氰化物 (DMC)络合物催化剂 ,以X 射线衍射、元素分析、红外光谱等手段进行了表征 ,考察了该催化体系下环氧丙烷开环聚合的反应特性 ,并初步探讨了聚合反应的机理 .研究发现 ,Co Zn双金属氰化物催化剂具有很高的催化活性 ,适合于中高分子量聚醚的合成 ,但是碱性起始剂起阻聚作用 ;在该催化体系下聚合物分子量可控 ,不饱和度很低 (<0 .0 14meq g) ,分批加料聚合所得到的聚合物分子量分布较窄 (Mn Mw <1.4 ) ,而一步加料聚合所得到的聚合物分子量分布变宽 ;1 3C NMR分析表明聚合物主链具有无规立构分布的特点 ,且链节分布几乎都为头 尾方式 .聚合过程中活性链与非活性链之间可能存在一个交换反应 ;虽然聚合反应有终止 ,但与聚合物链长没有关系 ,聚合物链的终止是可逆的 . 相似文献