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91.
Pd(OAc)2/FePc催化环己烯氧化合成环己酮的研究 总被引:6,自引:0,他引:6
考察了几种Fe-大环配合物与Pd(OAc)2组成的双组分催化体系,在乙腈酸性水溶液中环己烯经合成环己酮的催化活性,实验结果表明,其中以酞菁失(FePc)与Pd(OAc)2组成的催化体系活性最高,而FeTPPCl与Pd(OAc)2催化体系,虽然催化活性较高,但催化剂的稳定性较低,各种因素对Pd(OAc)2/FePc催化活催化影响的研究结果指出,在无水和酸存在的非水溶液中,Pd(OAc)2/FePc对 相似文献
92.
93.
A simple and rapid capillary electrophoretic method was developed for the simultaneous determination of noradrenaline (NA) and dopamine (DA) in Portulaca oleracea L. The buffer solution used in this method was 40 mM tris (hydroxymethyl) aminomethane (Tris)-H3PO4 at pH 2.00 containing 15% methanol. The effects of pH value, organic modifier, and applied voltage were investigated. The linear ranges of NA and DA were 0.5-100 microg/mL (r=0.9952) and 6.25-200 microg/mL (r=0.9992), respectively. The relative standard deviations of the corrected peak area were 6.73% and 4.26%, respectively. NA and DA in Portulaca oleracea L. were simultaneous determined successfully within 5.6 min. In this way, the contents of NA and DA in different parts (stem, leaves, and seeds) of P. oleracea L. and in different extracts of leaves with different solvents (distilled water, 50% methanol, and methanol) were studied. 相似文献
94.
YueMingLIU FengMeiZHANG HaiHongWU HaiJiaoZHANG JianGuoYANG XingTianSHU MingYuanHE 《中国化学快报》2004,15(10):1258-1260
A SAPO-11 silicoaluminophosphate molecular sieve with stable crystal structure was synthesized for the first time. After removing template by calcination, its crystal space group still retains Icm2 which the as-synthesized has. The catalyst deriving from the present SAPO-I 1 materials shows higher isomerization selectivity and higher paraffin hydroisomerization yield than those reported elsewhere. 相似文献
95.
96.
从氨性柠檬酸溶液中电沉积Ni-Mo的机理研究 总被引:6,自引:1,他引:6
含钼大于约27%(质量分数)Ni-Mo合金,具有较高的耐蚀性,特别是在盐酸和硫酸溶液中,其耐蚀性优于SUS304不锈钢[1].因此,人们对该种合金的电沉积进行了广泛的研究[1-4].对合金共沉积机理也作了一定的研究.一般认为,钼不能单独进行电沉积,但它可以同铁族元素共沉积[5].对钼与铁族元素的共沉积机理,人们已提出了几种假设.一般认为[3],钼可能是多步还原,即六价钼首先被电化学还原成低价钼化合物,而后由吸附在诱导金属(铁族元素)上的原子氢进一步还原成合金中的零价钼,为了进一步弄清Ni-Mo合金的共沉积机理,本… 相似文献
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98.
We introduce the concept of a twisting cochain and a twisted complex associated to a coherent sheaf. For sheaves of submanifolds these twisted complexes are used to construct on cochain level the Grothendieck theory of dual class and Gysin map. These explicit constructions give, for instance, a local formula for dual class of higher codimensional submanifolds. We prove a refined version of the Hirzebruch Riemann Roch using such local formulas. We also prove a theorem on when global analytic intersection classes can be computed from first order geometric data. This theory will be used to prove the Holomorphic Lefschetz formula (in Part II) and the Hirzebruch Riemann Roch for analytic coherent sheaves.The first author is supported in part by NSF grants GP-36418X1 and MCS 76-08478. The second by MCS 75-07986 and Sonderforschungsbereich Theoretische Mathematik at Bonn University 相似文献
99.
Two new ent‐abietane diterpenoids, macrophynin E ( 1 ) and macrophynin F ( 2 ), and a known related ent‐abietanoid (?)‐lambertic acid ( 3 ), together with four known ent‐kauranoids, were isolated from the roots and aerial parts of Isodon macrophylla, respectively. The structures of the new compounds were elucidated on the basis of spectroscopic‐data analysis and chemical correlations. 相似文献
100.
The retention and selectivity of the chromatographic separation of basic (cationic) analytes on a polybutadiene-coated zirconia (PBD-ZrO2) stationary phase have been studied in greater detail than in previous studies. These separations are strongly influenced by the chemistry of the accessible surface of zirconia. In the presence of buffers which contain hard Lewis bases (e.g., phosphate, fluoride, carboxylic acids) zirconia's surface becomes negatively charged due to adsorption of the buffer anion at the hard Lewis acid sites. Consequently, under most conditions (e.g., neutral pH), cationic analytes undergo both hydrophobic and cation-exchange interactions. This mixed-mode retention process generally leads to greater retention factors for cations relative to those on silica-based reversed phases despite the lower surface areas of the zirconia phase, but, more importantly, adsorption of hard Lewis bases can be used to control the chromatographic selectivity for cationic analytes on these zirconia-based stationary phases. In contrast to our prior work, here we show that when mixed-mode retention takes place, both retention and selectivity are easily adjusted by changing the type of hard Lewis base buffer anion, the type of buffer counter-ion (e.g., sodium, potassium, ammonium), the pH, and the ionic strength of the eluent as well as the type and amount of organic modifier. 相似文献