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61.
John Nicolson Low Celeste Garcia Manuel Melguizo Justo Cobo Adolfo Snchez Manuel Nogueras M. D. Lpez 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(11):e526-e527
The title compound, C25H29N3O13S, has peripheral acetyl and carbomethoxy groups which show disorder. The absolute structure, although known from the starting materials, was confirmed by the analysis. There are no intermolecular hydrogen bonds. This structure is of importance because it elucidates the pathway for hetero‐Diels–Alder reactions between dimethyl acetylenedicarboxylate and 6‐aminopyridin‐4(3H)‐one derivatives catalyzed by trifluoroacetic acid. 相似文献
62.
Tricyclic basic dyes (proflavine, acridine orange, pyronine, pyronine Y, oxonine, thionine and methylene blue) often form one‐to‐one or two‐to‐one complexes with CB[7] and CB[8], respectively. In the case of pyronine Y, the complexes with CB[7] and CB[8] have a one‐to‐one and three‐to‐one stoichiometry, respectively. The binding constants for CB[7] complexes range from 3.07×106 to 1.70×107 m ?1. In the case of CB[8], the association constant varies between 3.24×1013 and 2.50×1016 m ?2. Overall, these binding constants are four orders of magnitude higher than those reported for the same dyes in β and γ‐cyclodextrins. Formation of the host–guest complexes leads to an increase in the fluorescence quantum yields in the case of CB[7], while the dimeric or trimeric dye encapsulated in CB[8] are remarkably less fluorescent than the same dye in diluted solutions. 相似文献
63.
Smith EF Garcia IJ Briggs D Licence P 《Chemical communications (Cambridge, England)》2005,(45):5633-5635
The in situ monitoring of catalysis in Room Temperature Ionic Liquids (RTILs) is fundamental to the understanding of catalytic processes and the role of RTILs in catalytic turnover; we describe how XPS can be used to give information on both pure RTILs and catalytically-active RTIL-based solutions. 相似文献
64.
E. I. Klimova E. A. Vazquez Lopez T. Klimova M. Martinez Garcia Ortega S. Hernandez L. Ruiz Ramirez 《Russian Journal of General Chemistry》2004,74(11):1757-1762
Ferrocenyltetrahydropyrimidin-2-ones were prepared by reactions of linear and cyclic ,-unsaturated ketones of the ferrocene series with urea in i-PrOH in the presence of t-BuOK. The structures of the compounds prepared were studied by 1H and 13C NMR and IR spectroscopy, and also by single crystal X-ray diffraction.Translated from Zhurnal Obshchei Khimii, Vol. 74, No. 11, 2004, pp. 1887–1893.Original Russian Text Copyright © 2004 by E. Klimova, Lorez, T. Klimova, Garcia, Hernandez, Ramirez.This revised version was published online in April 2005 with a corrected cover date. 相似文献
65.
Amanda C. Garcia Thomas Touzalin Celine Nieuwland Nickson Perini Marc T. M. Koper 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(37):13133-13137
Herein, the effect of the alkali cation (Li+, Na+, K+, and Cs+) in alkaline electrolytes with and without Fe impurities is investigated for enhancing the activity of nickel oxyhydroxide (NiOOH) for the oxygen evolution reaction (OER). Cyclic voltammograms show that Fe impurities have a significant catalytic effect on OER activity; however, both under purified and unpurified conditions, the trend in OER activity is Cs+ > Na+ > K+ > Li+, suggesting an intrinsic cation effect of the OER activity on Fe‐free Ni oxyhydroxide. In situ surface enhanced Raman spectroscopy (SERS), shows this cation dependence is related to the formation of superoxo OER intermediate (NiOO?). The electrochemically active surface area, evaluated by electrochemical impedance spectroscopy (EIS), is not influenced significantly by the cation. We postulate that the cations interact with the Ni?OO? species leading to the formation of NiOO??M+ species that is stabilized better by bigger cations (Cs+). This species would then act as the precursor to O2 evolution, explaining the higher activity. 相似文献
66.
Haraguchi SK Silva AA Vidotti GJ dos Santos PV Garcia FP Pedroso RB Nakamura CV de Oliveira CM da Silva CC 《Molecules (Basel, Switzerland)》2011,16(2):1166-1180
A series of new thiosemicarbazones derived from natural diterpene kaurenoic acid were synthesized and tested against the epimastigote forms of Trypanosoma cruzi to evaluate their antitrypanosomal potential. Seven of the synthesized thiosemicarbazones were more active than kaurenoic acid with IC?? values between 2-24.0 mM. The o-nitro-benzaldehyde-thiosemicarbazone derivative was the most active compound with IC?? of 2.0 mM. The results show that the structural modifications accomplished enhanced the antitrypanosomal activity of these compounds. Besides, the thiocyanate, thiosemicarbazide and the p- methyl, p-methoxy, p-dimethylamine, m-nitro and o-chlorobenzaldehyde-thiosemicarbazone derivatives displayed lower toxicity for LLMCK? cells than kaurenoic acid, exhibing an IC?? of 59.5 mM. 相似文献
67.
A. B. Garcia E. R. Galán J. A. S. Blázquez C. V. Calahorro 《Journal of Thermal Analysis and Calorimetry》1986,31(2):247-251
The thermal behaviour of some 2-benzylamino-2-deoxyheptonic acids obtained from 2-benzylamino-2-deoxy-D-glycero-L-gluco, 2-benzylamino-2-deoxy-D-glycero-D-ido and 2-benzylamino-2-deoxy-D-glycero-D-taloheptononitriles (reported) previously has been studied in air (static atmosphere) and N2 (dynamic atmosphere, flow rate 200 ml/min).
Zusammenfassung Das thermische Verhalten einiger aus 2-Benzylamino-2-desoxy-D-glycero-L-gluco-, 2-Benzylamino-2-desoxy-D-glycero-D-ido und 2-Benzylamino-2-desoxy-D-glycero-D-talo-heplononitril (kürzlich beschrieben) erhaltenen 2-Benzylamino-2-desoxy-heptonsäuren wurde ín Luft (statische Atmosphäre) und N2 (dynamische Atmosphäre, Strömungsgeschwindigkeit 200 ml/min) untersucht.
( 200 /) 2--2- , 2--2---uepo-L, 2-2- ---- 2-2--- -- 2--2----ma .相似文献
68.
J. M. Garcia de la Vega B. Miguel E. San Fabian 《International journal of quantum chemistry》1997,61(3):533-540
Density functional (DF) calculations of the tetrachloromethane cation and its most important competitive process, the formation of CCl+3, were carried out to explain the possible stability of CCl+4. From results obtained with B-LYP and B-P86 methods, it is possible to produce a slight Jahn-Teller (JT) effect for a Cs planar structure of the cation type CCl2(SINGLE BOND)Cl(SINGLE BOND)Cl+ compatible with the experimental data obtained by electron-spin resonance spectroscopy. A complex of C3v structure CCl+3(SINGLE BOND)Cl which is similar to the previous one found in CF+4 appears when symmetry-broken wave functions are used in HF-LYP and HF-P86 methods. Depending of the DF method employed, either one of the minima [Cs (planar) and C3v] is the most stable and competes with the dissociation of the molecular ion to give CCl+3. The JT stabilization energy is smaller when the JT active coordinates are considered. © 1997 John Wiley & Sons, Inc. 相似文献
69.
Thermolysis of a 2'-[(16)O]-O-benzoyl-[(17)O]-5'-O-(tert-butyldimethylsilyl)-O(2),3'-cyclouridine derivative gave the more stable 3'-[(17)O]-O-benzoyl-[(16)O]- 5'-O-(tert-butyldimethylsilyl)-O(2),2'-cyclouridine isomer, which was converted into 3'-[(17)O]-2'-azido-2'-deoxyuridine by deprotection and nucleophilic ring opening at C2' with lithium azide. The 5'-diphosphate was prepared by nucleophilic displacement of the 5'-O-tosyl group with tris(tetrabutylammonium) hydrogen pyrophosphate. Model reactions gave (16)O and (18)O isotopomers, and base-promoted hydrolysis of an O(2),2'-cyclonucleoside gave stereodefined access to 3'-[(18)O]-1-(beta-D-arabinofuranosyl)uracil. Inactivation of ribonucleoside diphosphate reductase with 2'-azido-2'-deoxynucleotides results in appearance of EPR signals for a nitrogen-centered radical derived from azide, and 3'-[(17)O]-2'-azido-2'-deoxyuridine 5'-diphosphate provides an isotopomer to perturb EPR spectra in a predictable manner. 相似文献
70.
Klimova-Berestneva T. Martinez Garcia M. Meleshonkova N. N. Klimova E. I. 《Russian Journal of General Chemistry》2001,71(10):1626-1631
The asymmetric induction in the synthesis of 3,4,5-trisubstituted 4,5-dihydropyrazoles with ferrocenyl substituents, starting from the E and Z isomers of ,-unsaturated ketones was studied. A high diastereoselectivity was revealed at the 1,2 chiral center chiral center induction, which is independent of the configuration of the starting chalcones. 相似文献