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61.
合成了含Mo(0)的三核化合物(Et4N)2[(CO)4Mo(μ-S)2Mo(μ-S)2Mo(CO)4](Ⅰ)和(Et4N)2[(CO)4Mo(μ-S)2W(μ-S)2Mo(CO)4](Ⅱ),测定了(Ⅰ)的晶体结构.Ⅰ属单斜晶系,空间群P2相似文献
62.
氨基酸植物组织传感器的研究 总被引:3,自引:0,他引:3
选择苹果及仙人球的组织切片作生物催化材料,同氨气敏电极组合,研制了2种对L-谷氨酰胺及L-天冬酰胺选择响应的新型的组织传感器。研究和讨论了传感器的最佳工作条件。用该组织传感器测定了L-天冬酰胺脱氨酶和L-谷氨酰胺脱氨酶的动力学参数K_m和V_m。 相似文献
63.
64.
K. W. Cheah L. C. Ho J. B. Xia J. Li W. H. Zheng W. R. Zhuang Q. M. Wang 《Applied Physics A: Materials Science & Processing》1995,60(6):601-606
Photoluminescence studies on porous silicon show that there are luminescence centers present in the surface states. By taking photoluminescence spectra of porous silicon with respect to temperature, a distinct peak can be observed in the temperature range 100–150 K. Both linear and nonlinear relationships were observed between excitation laser power and the photoluminescence intensity within this temperature range. In addition, there was a tendency for the photoluminescence peak to red shift at low temperature as well as at low excitation power. This is interpreted as indicating that the lower energy transition becomes dominant at low temperature and excitation power. The presence of these luminescence centers can be explained in terms of porous silicon as a mixture of silicon clusters and wires in which quantum confinement along with surface passivation would cause a mixing of andX band structure between the surface states and the bulk. This mixing would allow the formation of luminescence centers. 相似文献
65.
Wen-bao Li Ya-hui Zhuang Dai-zheng Liao Geng-ling Wang 《Transition Metal Chemistry》1994,19(3):315-318
Summary Two -phenoxo-bridged binuclear copper(II) complexes, [Fsal(GG)2Cu2Cl3]·H2O (1) containing an exogenous chloride-bridge and [Fsal(GG)2Cu2(OH)](ClO4)2·H2O (2) containing an exogenous hydroxide-bridge, where {Fsal(GG)2 = 2,6-bis[N-(acetylglycine)-imino-methylene]-4-methylphenol}, were synthesized. The complexes were characterized be several spectroscopic methods. According to variable temperature magnetic susceptibility measurements (4–300 K), the hydroxide-bridged complex (2) has a weak antiferromagnetic spin exchange integral (J =- 23.6 cm), while the chloride complex (1) has an unusual weak ferromagnetic spin exchange integral (J = + 30.9 cm); both complexes have similar optical spectra in the aqueous solutions. 相似文献
66.
The kinetics of the acid catalyzed hydrolysis of 2-aminoethanethiolsulfate (AETS) ions were investigated. The dependence of the hydrolysis rate constant on acidity and temperature was determined. The hydrolysis rate equation can be expressed as where Ho is the Hammett acidity function. The rate constant, k, can be expressed as The pKa's for the compound were measured and literature value of pKa was found to be in error. The values determined in this study are pKa1 < ?0.5 and pKa2 = 9.1 ± 0.1. General acid catalysis of the hydrolysis reaction was found not to proceed to a significant degree. © 1994 John Wiley & Sons, Inc. 1 This article is a US Government work and, as such, is in the public domain in the United States of America. 相似文献
67.
SynthesisandStructureof[(C_2H_5)_4N][Mo_3(μ_3-O)(μ-Cl)_3(μ-CH_3CH_2COO)_3Cl_3]ZhuangHong-Hui;WuDing-Ming;HuangJian-Quan;HuangJin-L... 相似文献
68.
Jian Zhuang Julius M. Hastings Lester M. Corliss R. Bau Chiau-Yu Wei R. O. Moyer Jr. 《Journal of solid state chemistry》1981,40(3):352-360
Neutron diffraction data have been collected on a powdered sample of Sr2IrD5 over a range of temperatures. The compound, which is cubic at room temperature, has been found to exhibit a gradual transformation to a tetragonal phase in the temperature range 200-140 K. As a result of the transition, deuterium atoms which randomly occupy sixfold positions in the cubic phase, become tetragonally ordered. A small fraction of the cubic phase remained untransformed at 4.2 K. Both the cubic and tetragonal structures are consistent with square pyramidal IrD5 units with average Ir---D distances of 1.714 and 1.718 Å, respectively. Agreement factors, R1, for the two structural analyses are 3.44 and 4.94%. 相似文献
69.
70.
对流层夜间化学研究 总被引:1,自引:0,他引:1
NO3自由基与N2O5是对流层夜间化学的关键物种。一方面NO3与O3等组分是夜间大气中的重要氧化剂,与它们的反应是生物排放挥发性有机物(VOCs)的主要汇;另一方面NO3与N2O5和雨滴或气溶胶颗粒物发生的异相反应则是大气中氮氧化合物NOx(NO,NO2)的主要清除过程,从而可以减轻对流层臭氧污染。研究它们的化学反应性质及对其进行实地测量,对深入理解大气氧化过程和全面了解区域乃至全球大气自净能力有重要意义。本文总结了近年来有关夜间化学的研究成果,介绍了以NO3和N2O5为中心的基本夜间化学过程、对流层中NO3与N2O5的源与汇以及外场测量技术的最新研究进展,并提出了尚待解决的一些问题。 相似文献