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21.
D. Yu. Naumov A. V. Virovets S. V. Korenev A. I. Gubanov 《Acta Crystallographica. Section C, Structural Chemistry》1999,55(8):IUC9900097-IUC9900097
22.
S. A. Adonin A. V. Virovets M. N. Sokolov V. P. Fedin 《Russian Journal of Coordination Chemistry》2010,36(10):734-738
New cluster complexes [W3S4(Acac)3(PPh3)3]PF6 · 0.5CHCl3 (Acac = CH3C(O)CHC(O)CH3) (I) and [W3S4(Hfac)3(PPh3)2Br] · 2CHCl3 (Hfac = CF3C(O)CHC(O)CF3) (II) were synthesized. Their molecular and crystal structures were determined by X-ray diffraction. The cis-cis type of coordination of acetylacetonate and hexafluoroacetylacetonate ligands in I and II, respectively, was established, and the PPh3 ligands were found in the trans-positions with respect to the “capping” sulfide ligand (μ3-S). 相似文献
23.
L. B. Serezhkina E. V. Peresypkina A. V. Virovets D. V. Pushkin A. G. Verevkin 《Crystallography Reports》2010,55(3):381-385
The synthesis and single-crystal X-ray diffraction study of Cs[UO2(SeO4)(OH)] · 1.5H2O (I) and Cs[UO2(SeO4)(OH)] · H2O (II) are performed. Compound I crystallizes in the monoclinic crystal system, a = 7.2142(2) Å, b = 14.4942(4) Å, c = 8.9270(3) Å, β = 112.706(1)°, space group P21/m, Z = 4, and R = 0.0222. Compound II is monoclinic, a = 8.4549(2) Å, b = 11.5358(3) Å, c = 9.5565(2) Å, β = 113.273(1)°, space group P21/c, Z = 4, and R = 0.0219. The main structural units of crystals I and II are [UO2(SeO4)(OH)]? layers which belong to the AT 3 M 2 crystal chemical group of uranyl complexes (A = UO 2 2+ , T 3 = SeO4 2?, and M 2 = OH?). In structure I, johannite-like layers are found. Structure II is a topological isomer of I. The two structures differ in the number of U(VI) atoms bound to the central atom by all bridging ligands. 相似文献
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A. V. Virovets E. V. Lider V. N. Elokhina M. B. Bushuev L. G. Lavrenova 《Journal of Structural Chemistry》2005,46(2):358-362
1,2,4-Triazole derivative substituted in the 4th position — 4-(3,4-dichlorphenyl)-1,2,4-tirazole — has been synthesized. Crystal and molecular structure of the compound were determined by single crystal X-ray diffraction. Molecular geometry optimization and effective charge calculations were performed by DFT methods. 相似文献
28.
Cover Picture: Metal‐Free Addition/Head‐to‐Tail Polymerization of Transient Phosphinoboranes,RPH‐BH2: A Route to Poly(alkylphosphinoboranes) (Angew. Chem. Int. Ed. 46/2015) 下载免费PDF全文
29.
Redox and Coordination Behavior of the Hexaphosphabenzene Ligand in [(Cp*Mo)2(μ,η6:η6‐P6)] Towards the “Naked” Cations Cu+, Ag+, and Tl+ 下载免费PDF全文
Martin Fleischmann Fabian Dielmann Laurence J. Gregoriades Eugenia V. Peresypkina Alexander V. Virovets Sebastian Huber Alexey Y. Timoshkin Gbor Balzs Manfred Scheer 《Angewandte Chemie (International ed. in English)》2015,54(44):13110-13115
Although the cyclo‐P6 complex [(Cp*Mo)2(μ,η6:η6‐P6)] ( 1 ) was reported 30 years ago, little is known about its chemistry. Herein, we report a high‐yielding synthesis of 1 , the complex 2 , which contains an unprecedented cyclo‐P10 ligand, and the reactivity of 1 towards the “naked” cations Cu+, Ag+, and Tl+. Besides the formation of the single oxidation products 3 a,b which have a bisallylic distorted cyclo‐P6 middle deck, the [M( 1 )2]+ complexes are described which show distorted square‐planar (M=Cu( 4 a ), Ag( 4 b )) or distorted tetrahedral coordinated (M=Cu( 5 )) M+ cations. The choice of solvent enabled control over the reaction outcome for Cu+, as proved by powder XRD and supported by DFT calculations. The reaction with Tl+ affords a layered two‐dimensional coordination network in the solid state. 相似文献
30.
P. A. Petrov A. V. Virovets P. E. Plyusnin E. Yu. Filatov I. V. El’tsov Ya. Z. Voloshin S. N. Konchenko 《Russian Journal of Inorganic Chemistry》2014,59(10):1162-1167
A ribbed-monofunctionalized macrobicyclic iron(II) complex with tert-butyl sulfide substituents has been prepared via nucleophilic substitution of its dichloroclathrochelate precursor with tert-butylthiolate ion. This new complex has been characterized using elemental analysis, IR and multinuclear NMR spectroscopy, and the single crystal X-ray diffraction. Its thermal destruction occurs with release of isobutylene and polyunsaturated hydrocarbons giving iron borate, iron fluoropolyborate, and iron nitride as follows from combined thermal analysis and X-ray powder diffraction data. 相似文献