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Stepan Boitsov Jon Songstad Karl W. Trnroos 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(2):o66-o68
4‐(Trifluoromethyl)benzonitrile, C8H4F3N, at 123 K contains molecules linked together through one C—H?F bond and two C—H?N hydrogen bonds into sheets that are further crosslinked to form a dense two‐dimensional network without π?π ring interactions. The aromatic ring is slightly deformed due to the two para‐related electronegative groups. 相似文献
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Smith MD Stepan AF Ramarao C Brennan PE Ley SV 《Chemical communications (Cambridge, England)》2003,(21):2652-2653
Palladium-containing perovskites (LaFe0.57Co0.38Pd0.05O3) have been exploited as recoverable and reuseable catalysts in Suzuki coupling reactions; residual levels of Pd after removal of the catalyst by filtration are low (2 ppm) despite evidence that the reaction is occurring via a homogeneous process. 相似文献
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Stepan S. Basok Gabriele Bocelli Eduard V. Ganin Marina S. Fonari Yurii A. Simonov 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(1):o50-o52
In the title compound, 2C8H18NO3+·2C7H6NO2−·3H2O, proton transfer occurs from the carboxylic acid group of the 4‐aminobenzoic acid (PABA) molecule to the amine group of the macrocycle, resulting in the formation of a salt‐like adduct. The anions are combined into helical chains which are further bound by the water molecules into sheets. The macrocyclic cations are situated between these layers and are bound to the anions both directly and via bridging water molecules. The structure exhibits a diverse system of hydrogen bonding. 相似文献
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Juan Chen Stepan Stepanovic Dr. Apparao Draksharapu Prof. Dr. Maja Gruden Prof. Dr. Wesley R. Browne 《Angewandte Chemie (International ed. in English)》2018,57(12):3207-3211
Non‐heme (L)FeIII and (L)FeIII‐O‐FeIII(L) complexes (L=1,1‐di(pyridin‐2‐yl)‐N,N‐bis(pyridin‐2‐ylmethyl)ethan‐1‐amine) underwent reduction under irradiation to the FeII state with concomitant oxidation of methanol to methanal, without the need for a secondary photosensitizer. Spectroscopic and DFT studies support a mechanism in which irradiation results in charge‐transfer excitation of a FeIII?μ‐O?FeIII complex to generate [(L)FeIV=O]2+ (observed transiently during irradiation in acetonitrile), and an equivalent of (L)FeII. Under aerobic conditions, irradiation accelerates reoxidation from the FeII to the FeIII state with O2, thus closing the cycle of methanol oxidation to methanal. 相似文献
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Nicolaou KC Stepan AF Lister T Li A Montero A Tria GS Turner CI Tang Y Wang J Denton RM Edmonds DJ 《Journal of the American Chemical Society》2008,130(39):13110-13119
The molecular design, chemical synthesis, and biological evaluation of two distinct series of platensimycin analogues with varying degrees of complexity are described. The first series of compounds probes the biological importance of the benzoic acid subunit of the molecule, while the second series explores the tetracyclic cage domain. The biological data obtained reveal that, while the substituted benzoic acid domain of platensimycin is a highly conserved structural motif within the active compounds with strict functional group requirements, the cage domain of the molecule can tolerate considerable structural modifications without losing biological action. These findings refine our present understanding of the platensimycin pharmacophore and establish certain structure-activity relationships from which the next generation of designed analogues of this new antibiotic may emerge. 相似文献
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Stepan Oryshchyn Volodymyr Babizhetskyy Olga Zhak Jean-Yves Pivan Arndt Simon 《Journal of solid state chemistry》2010,183(11):2534-2543
The new ternary pnictides Er12Ni30P21 and Er13Ni25As19 have been synthesized from the elements. They crystallize with hexagonal structures determined from single-crystal X-ray data for Er12Ni30P21 (space group P63/m, a=1.63900(3) nm, c=0.37573(1) nm, Z=1, RF=0.062 for 1574 F-values and 74 variable parameters), and for Er13Ni25As19 (Tm13Ni25As19-type structure, space group P6?, a=1.6208(1) nm, c=0.38847(2) nm, Z=1, RF=0.026 for 1549 F-values and 116 variable parameters). These compounds belong to a large family of hexagonal structures with a metal-metalloid ratio of 2:1. HRTEM investigations were conducted to probe for local ordering of the disordered structure at the nanoscale. The magnetic properties of the phosphide Er12Ni30P21 have been studied in the temperature of range 2<T<300 K and with applied fields up to 5 T. The magnetic susceptibility follows the Curie-Weiss law from 4 to 300 K. The measured value of μeff=9.59 μB corresponds to the theoretical value of Er3+. 相似文献
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