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961.
利用表面放电光泵浦技术,研制了重频XeF(C-A)激光器,运行频率达到10 Hz。研究了运行频率、气体流量对激光输出能量稳定性的影响,分析了影响输出稳定性的主要因素,实验结果表明,提高气流量可有效改善重频输出能量的稳定性。同时,还给出了优化实验条件下不同运行频率连续20个脉冲较为理想的输出结果。运行频率分别为1,2,5 Hz时,输出能量稳定性较好,输出能量大于4.0 J;气流量大于53 L/s时,10 Hz重频运行的输出稳定性已显著提高,平均输出能量也达到1.8 J。 相似文献
962.
采用熔体快淬的方法制备Pr2Fe14B/α-Fe纳米晶复合永磁材料.使用振动样品磁强计(VSM)测量样品的室温磁性能.实验合金成分为(PrxFe94.3-xB5.7)0.99Zr1(其中x=8.2,8.6,9.0,9.4,9.8,10.2,10.6,11.0,11.4(原子分数,%)).系统地研究了辊速及合金成分对快淬带磁性能的影响,当Pr原子分数由8.
关键词:
纳米复合永磁材料
熔体快淬
2Fe14B/α-Fe')" href="#">Pr2Fe14B/α-Fe
磁性 相似文献
963.
964.
The organocatalysed asymmetric hydrosilylation of a number of N-aryl and alkyl β-substituted enamino esters proceeds in generally good yield and enantioselectivity. Crucial to obtaining high yield and selectivity was the addition of benzoic acid as an additive and under these conditions, both N-alkyl and N-aryl substituents were well tolerated. β-Aryl and alkyl substituents were evaluated and a model proposed to account for the experimental observations based upon enamine tautomerisation and conformational preferences of the reactive ketimine intermediate. 相似文献
965.
A model study of DNA-directed peptide ligation has been developed by transferring fluorescent reporting group from small molecule thioester to a DNA strand (template DNA) in the presence of a thiol-functionalized DNA strand (auxiliary DNA), mimicking the Native Chemical Ligation (NCL) reaction. This DNA-directed transfer shows dependence on the sequence complementarity of the two DNA strands, with in situ generated 4-thiolphenylmethyl functionalized oligonucleotide as the auxiliary DNA strand, under mild basic condition (pH=8.5), and with tris(2-carboxyethyl) phosphine hydrochloride (TCEP) as a reducing agent. Reactions with different amino acid α-thioesters resulted in varied transfer efficiencies from glycine to α-substituted amino acids. This study has provided the basic foundation to use DNA-programmed chemistry toward the chemical synthesis or unnatural modification of protein molecules. 相似文献
966.
Reported herein is the FeCl3-promoted intermolecular sulfoesterification of o-(1-alkynyl)benzoates with disulfides, which provides a convenient and efficient method for synthesis of 4-sulfenylisocoumarins. Various functional groups such as methoxy, halides, ester, cyano and silicon groups in the substrates are tolerated, and heterocycle-fused chalcogenylpyrones are also successfully achieved directly from the corresponding heterocyclic precursors under the same reaction conditions. In addition, starting from diynylbenzoate, this reaction sequence can be combined with a bicyclization step leading to the tetracyclic (E)-3-(2-phenyl-3-phenylchalcogenylinden-1-ylidene)isobenzofuranone frameworks with high regiospecificity and exclusive trans stereoselectivity. 相似文献
967.
A palladium-based catalyst (Fe3O4/SiO2/HPG–OPPh2–PNP) supported on chlorodiphenylphosphine-functionalized magnetic nanoparticles was successfully prepared from Fe3O4/SiO2 with sequential attachment of glycerol and chlorodiphenylphosphine, followed by treatment of an ethanolic solution of palladium chloride with hydrazine. The as-prepared catalyst was characterized by ICP-AES, FTIR, XRD, SEM, and TEM. The Fe3O4/SiO2/HPG–OPPh2–PNP was found as a magnetically separable and highly active catalyst for Suzuki coupling reactions of aryl iodides, bromides, and chlorides as well as Heck reactions of aryl iodides and bromides. Under appropriate conditions, all reactions afforded the desired products in moderate to excellent yields. Moreover, this catalyst can be easily recovered by using a magnetic field and directly reused for at least six cycles without significant loss of its activity. 相似文献
968.
δ-Glyconolactams were first synthesized by the intramolecular Schmidt–Boyer reaction using corresponding δ-azidosugars as starting material. The reaction could be efficiently performed in good yields of 61–69% under microwave radiation in acid condition, providing an alternative protocol to iminosugar δ-lactam. 相似文献
969.
The reaction of [60]fullerene with diethyl aminomalonate hydrochloride and carbon disulfide in the presence of triethylamine gave a [60]fullerene-fused thiolactam, which could be hydrolyzed, S-alkylated, and N-acylated in high yields. 相似文献
970.
Isomers based on the bisindolylmaleimide architecture were reported in this Letter. Introducing hydroxyl to this architecture lead to quenching the fluorescence of bisindolylmaleimide. The fluorescence was recovered with its hydroxyl group esterified. Ester group can be easily transformed to hydroxyl group by hydrolysis reaction. Thus, a toggle-switchable fluorescence, ‘off-on’ cycle can be established on the basis of reversible esterification/hydrolysis reaction. 相似文献