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Ushida N Kondo T Tasaka S Park IG Song JS Hara T Homma Y Tsuzuki Y Fujioka G Fukushima H Takahashi Y Tatsumi S Yokoyama C Fujiwara K Taruma K Bahk SY Kim CO Park JN Bailey DC Conetti S Mercure P Trischuk J Turcotte M Aoki S Chiba K Fuchi H Hoshino K Kodama K Matsui R Miyanishi M Nakamura M Nakazawa K Niu K Niwa K Ohashi M Sasaki H Tomita Y Torii N Yamakawa O Yanagisawa Y Aubrecht GJ Dunlea J Errede S Gauthier A Gutzwiller MJ Kuramata S Oleynik G Reay NW Reibel K Sidwell RA Stanton NR Moriyama K 《Physical review letters》1986,57(23):2897-2900
995.
Ushida N Kondo T Tasaka S Park IG Song JS Hara T Homma Y Tsuzuki Y Fujioka G Fukushima H Takahashi Y Tatsumi S Yokoyama C Fujiwara K Taruma K Bahk SY Kim CO Park JN Bailey DC Conetti S Mercure P Trischuk J Turcotte M Aoki S Chiba K Fuchi H Hoshino K Kodama K Matsui R Miyanishi M Nakamura M Nakazawa K Niu K Niwa K Ohashi M Sasaki H Tomita Y Torii N Yamakawa O Yanagisawa Y Aubrecht GJ Dunlea J Errede S Gauthier A Gutzwiller MJ Kuramata S Oleynik G Reay NW Reibel K Sidwell RA Stanton NR Moriyama K 《Physical review letters》1986,56(17):1771-1774
996.
Ushida N Kondo T Tasaka S Park IG Song JS Hara T Homma Y Tsuzuki Y Fujioka G Fukushima H Takahashi Y Tatsumi S Yokoyama C Fujiwara K Taruma K Bahk SY Kim CO Park JN Bailey DC Conetti S Mercure P Trischuk J Turcotte M Aoki S Chiba K Fuchi H Hoshino K Kodama K Matsui R Miyanishi M Nakamura M Nakazawa K Niu K Niwa K Ohashi M Sasaki H Tomita Y Torii N Yamakawa O Yanagisawa Y Aubrecht GJ Dunlea J Errede S Gauthier A Gutzwiller MJ Kuramata S Oleynik G Reay NW Reibel K Sidwell RA Stanton NR Moriyama K 《Physical review letters》1986,56(17):1767-1770
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The addition of C1-C7 alcohols (methanol, ethanol, propanol, butanol, heptanol, hexanol and heptanol) to dilute sulfuric acid as eluent in ion-exclusion chromatography using a highly sulfonated styrene-divinylbenzene co-polymer resin (TSKgel SCX) in the H+ form as the stationary phase was carried out for the simultaneous separations of both (a) C1-C7 aliphatic carboxylic acids (formic, acetic, propionic, isobutyric, butyric, isovaleric, valeric, 2-methylvaleric, isocaproic, caproic, 2,2-dimethyl-n-valeric, 2-methylhexanoic, 5-methylhexanoic and heptanoic acids) and (b) benzenecarboxylic acids (pyromellitic, hemimellitic, trimellitic, o-phthalic, m-phthalic, p-phthalic, benzoic and salicylic acids and phenol). Heptanol was the most effective modifier in ion-exclusion chromatography for the improvement of peak shapes and a reduction in retention volumes for higher aliphatic carboxylic acids and benzenecarboxylic acids. Excellent simultaneous separation and relatively highly sensitive conductimetric detection for these C1-C7 aliphatic carboxylic acids were achieved on the TSKgel SCX column (150 x 6 mm I.D.) in 30 min using 0.5 mM sulfuric acid containing 0.025% heptanol as eluent. Excellent simultaneous separation and highly sensitive UV detection at 200 nm for these benzenecarboxylic acids were also achieved on the TSKgel SCX column in 30 min using 5 mM sulfuric acid containing 0.075% heptanol as eluent. 相似文献
999.
A simple, rapid and reliable capillary electrophoresis method with a photodiode array detector was developed for determination of azide as the 3,5-dinitrobenzoyl derivative in drink samples fortified with sodium azide. Sample preparation was simple and rapid because no more than a simple dilution of samples is needed after quick derivatization. Separation was carried out using a buffer system comprising 25 mM phosphate buffer and 4 mM cetyltrimethylammonium hydroxide at pH 3.0. Methyl benzoate was selected as the internal standard (IS). This study investigated the influence of the concentration of phosphate buffer and electroosmotic flow (EOF) modifier, and the buffer pH on migration time and signal response. The optimized method made it possible to determine azide within 5 min. The limit of detection was determined to be 1.9 microg/ml with SIN > 3. The quantitation range was 6.5-323 microg/ml. By the method recoveries of azide in drink samples fortified with sodium azide were investigated. Mean recovery values ranged from 93.6 to 105.8% and results were satisfactory. In addition, no interference was observed in electropherograms of drink samples fortified with sodium azide. Thus, by this method, azide in drink samples can be determined rapidly with high recoveries and good selectivity despite extremely simple sample preparation. 相似文献
1000.
The actual structures of the four stereoisomers of serricornin were examined by the X-ray analysis and high-field pmr spectroscopy. Each of the stereoisomers assumes either or both of two forms, cyclic hemiacetal and acyclic chain, in solution. 相似文献