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71.
INTRODUCTION Epoxy resins are reactive polymers which when cured with a variety of chemicals lead to a host of useful thermosets. Since the epoxide is a strained ring, it readily undergoes addition and homopolymerization. The homopolymerization is a process catalysed by acids, bases, Lewis acids, t-amines as well as by inorganic salts. 相似文献
72.
M. K. Mamedov A. G. Piraliev R. A. Rasulova 《Russian Journal of Applied Chemistry》2007,80(12):2085-2089
New reactive monomers, bicyclo[2.2.1]hept-2-yloxyethyl acrylates, were prepared by esterification of monoethers derived from ethylene glycol and bicyclic alcohols with acrylic acid, using naphthalene-1,5-disulfonic acid as a new effective catalyst. The related propionates and isobutyrates were prepared by hydrogenation of these acrylates. 相似文献
73.
Shabanov A. L. Gasanova M. M. Mamedov Ch. I. 《Russian Journal of Organic Chemistry》2002,38(7):1060-1063
Stereochemistry of [2+2]- and [1+1]-macrocylization of cis-4-cyclohexene-1,2-dicarboxylic acid with 1,2-dibromoethane, 1,3-dichloro-2-propanol, and 1,5-dichloro-3-oxapentane was studied. The reaction of cis-4-cyclohexene-1,2-dicarboxylic acid with 1,2-dibromoethane according to the [2+2]-cyclization scheme gave a mixture of stereoisomeric macroheterocycles with cis,syn,cis- and cis,anti,cis-junction of the polyether and cyclohexene rings. In the reaction of cis-4-cyclohexene-1,2-dicarboxylic acid with 1,5-dichloro-3-oxapentane, a mixture of crown compounds with cis,anti,cis- and cis-junction of the polyether and cyclohexene rings was obtained. The structure of the products was established on the basis of their chemical transformations and spectral data. 相似文献
74.
V. A. Mamedov V. N. Valeeva L. A. Antokhina G. M. Doroshkina A. V. Chernova I. A. Nuretdinov 《Chemistry of Heterocyclic Compounds》1993,29(5):607-611
The methyl ester and N,N-diethylamide of 2-azido-5-phenyl-4-thiazolecarboxylic acid were obtained by the reaction of the corresponding 4-substituted 2-hydrazino-5-phenylthiazole with NaNO2 in acid media. IR and UV spectroscopy were used to show that the compounds synthesized retain azide form in both the crystalline state and in solution. The reaction of azides with dicarbonyl compounds gave derivatives of 2-[5-methyl-4-acetyl-or 2-[5-methyl-4-ethoxycarbonyl-1,2,3-triazol-1-yl]-5-phenylthiazole-4-carboxylic acid.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 710–714, May, 1993. 相似文献
75.
É. A. Mamedov 《Theoretical and Experimental Chemistry》1988,24(3):356-359
Based on the mechanism of oxidative dimerization of hydrocarbons the rules for the selection of catalysts for this kind of reactions has been discussed. It has been shown that an efficient dehydrodimerization catalyst must contain on its surface electron acceptor centers (metal cations) of moderate strength, strongly bound nucleophilic oxygen, and possess the corresponding collective properties. The elements have been discussed, the oxides of which satisfy the above requirements.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 24, No. 3, pp. 366–370, May–June, 1988. 相似文献
76.
3-[1′(1′H)-Substituent-pyrazol-5′-yl]benzo[5,6]coumarins and 3-(1′,2′-oxazol-5′-yl)benzo[5,6]coumarin were prepared via condensation of 3-(2′-formyl-1′-chlorovinyl)benzo[5,6] coumarin with hydrazine derivatives or hydroxylamine.Reaction of 3-[1′(1′H)-pyrazol-5′-yl]benzo[5,6]coumarin with alkyl halides,olefinic compunds or acid chlorides are described. 相似文献
77.
Jia‐Xiang Yang Yu‐Peng Tian Qing‐Liang Liu Yong‐Shu Xie Hoong‐Kun Fun Suchada Chantrapromma Ibrahim Abdul Razak 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(1):m43-m44
In the title compound, [Fe(C5H5)(C16H12N3OS)], the 8‐aminoquinoline and acylthiourea moieties are almost planar. There are two perpendicular arrangements of the molecules in the crystal with slightly different conformations. The two cyclopentadienyl rings in each molecule are parallel and eclipsed. 相似文献
78.
We report experimentally measured cross sections for pressure broadening of ammonia inversion transitions by J=0, ortho-D2 at temperatures of 18-40 K. These measurements were made in a quasiequilibrium cell using the collisional cooling technique. Cross sections for broadening of the metastable (J,K)=(1, 1), (2, 2) and (3, 3) inversion transitions ranged from 67.5 A2 for (1, 1) at 20.0 K to 100.1 A2 for (3, 3) at 25.0 K. The J=0, ortho-D2 cross sections were found to be consistently larger than previously measured cross sections for low temperature broadening of NH3 by both He and H2. 相似文献
79.
Ayoko Godwin Adefikayo Iyun Johnson Femi El-Idris Ibrahim Faskari 《Transition Metal Chemistry》1992,17(1):46-49
Transition Metal Chemistry - The kinetics of the silver(I) ion catalysed reduction of peroxodisulphate by 12-tungstocobaltate(II) anion in aqueous HC1O4 has been studied. Although the reaction in... 相似文献
80.
Mohamed M. Shoukry Ibrahim M. Kenawy Ibrahim H. El-Haj 《Transition Metal Chemistry》1991,16(6):637-640
Summary The formation and equilibria of the binary and ternary palladium(II) complexes of diethylenetriamine (dien) with other selected amines have been investigated. The results of pH titration measurements allowed the calculation of equilibrium constants, characteristic for the binary and ternary complexes formed. The concentration distribution of various complex species was evaluated and the chelation mode ascertained by conductivity measurements. 相似文献