全文获取类型
收费全文 | 144990篇 |
免费 | 22596篇 |
国内免费 | 16268篇 |
专业分类
化学 | 99935篇 |
晶体学 | 1634篇 |
力学 | 8504篇 |
综合类 | 972篇 |
数学 | 18024篇 |
物理学 | 54785篇 |
出版年
2024年 | 470篇 |
2023年 | 2747篇 |
2022年 | 5083篇 |
2021年 | 5345篇 |
2020年 | 5725篇 |
2019年 | 5445篇 |
2018年 | 5021篇 |
2017年 | 4672篇 |
2016年 | 6821篇 |
2015年 | 6810篇 |
2014年 | 8367篇 |
2013年 | 10770篇 |
2012年 | 12839篇 |
2011年 | 13095篇 |
2010年 | 9164篇 |
2009年 | 8771篇 |
2008年 | 9297篇 |
2007年 | 8301篇 |
2006年 | 7701篇 |
2005年 | 6478篇 |
2004年 | 5056篇 |
2003年 | 4059篇 |
2002年 | 3730篇 |
2001年 | 3080篇 |
2000年 | 2711篇 |
1999年 | 2937篇 |
1998年 | 2448篇 |
1997年 | 2237篇 |
1996年 | 2233篇 |
1995年 | 1975篇 |
1994年 | 1768篇 |
1993年 | 1457篇 |
1992年 | 1283篇 |
1991年 | 1115篇 |
1990年 | 942篇 |
1989年 | 717篇 |
1988年 | 544篇 |
1987年 | 483篇 |
1986年 | 480篇 |
1985年 | 387篇 |
1984年 | 267篇 |
1983年 | 232篇 |
1982年 | 176篇 |
1981年 | 116篇 |
1980年 | 86篇 |
1979年 | 43篇 |
1977年 | 35篇 |
1976年 | 41篇 |
1975年 | 43篇 |
1957年 | 36篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
992.
993.
IntroductionMethaneandcarbondioxidearetWomaincompositionsforthegreenhouseeffectandtheworldglobewanningll].ItisbeneficialtoourlivingenviroIUnenttocontrolthereleaseofthesetwogases.Theconversionofmethanetothecommonfeedstocksynthesisgas(carbonmonoxideandhydro… 相似文献
994.
Chemistry is a central science. However, the public's recognition of chemistry needs to be promoted, and the prejudice needs to be reduced. Chemical science popularization is a long-term, complex and arduous social education project, which is of great significance to promote social harmony and improve people's quality of life. This paper summarizes the current status of chemical science popularization in China, and puts forward the innovative development countermeasures which focus on improving public participation, training popular science talents, carrying out popular science popularization education at different levels, creating high-quality science popularization works and opening up new positions and approaches of chemical science popularization. This paper has the reference value for the science popularization colleagues. 相似文献
995.
α-异丙基、β-异丁基丙烯酸希土配合物的合成和配位性质研究 总被引:3,自引:0,他引:3
本文制备了α-异丙基、β-异丁基丙烯酸的15种希土配合物RE(C9H17COO)3,用X射线多晶粉末衍射、电子光谱、红外光谱和热重差热分析方法研究了配合物中RE-O键的成键性能以及羧基的配位性质.配合物中存在两种不同的羧基配位形式,轻中希土配合物(La,Ce,Pr,Nd,Sm,Eu)中羧基具有不对称桥式双齿配位形式,而重希土配合物(Gd,Tb,Dy,Ho,Er,Tm,Yb,Lu,Y)中羧基具有对称螯合双齿配位形式,配位形式的不同使得希土配合物呈现两种不同的多晶衍射图和热分解过程. 相似文献
996.
The influence of additives such as sodium salicylate and sodium chloride on the water solubilization capacity of AOT in n-pentanol solutions has been investigated. The water solubilization capacity is enhanced by sodium salicylate and decreased by sodium chloride. The percolation behavior of the water/AOT/n-pentanol system is studied by modifying the water concentration and temperature. No percolation threshold induced by water or temperature is detected either in the absence or in the presence of additives. The values of ln sigma have a linear correlation with temperature in the range of 5-40 degrees C. The activation energy is also estimated and discussed. 相似文献
997.
A highly sensitive fluorimetric method for the determination of fluoride was established. The method was based on quenching of the fluorescence of the Al3+-calcein complex in CCl3COOH-CH3COOK buffer solution by fluoride. The fluorescence emission was measured at lambdaex/lambdaem 480/503 nm, and the experimental variables and interference in this determination were studied. The linear calibration range was 0.8 ng/mL to 150 ng/mL and the detection limit was 0.2 ng/mL. The method was applied to determine fluoride in biological materials. The recovery was in the range of 96.3% to 104.7% and the relative standard deviation was 4.6%. The results obtained from the certified reference material by the present method agreed with the certified values. 相似文献
998.
以邻苯二胺为原料合成表征了一类喹喔啉衍生物;1-烷基-3-甲基-2(1H)-喹喔啉-2-酮(1-alkyl-3-methly-2(1H)-quinoxalin-2-one,简称AMQ,其中alky=H、CH3、Et、n-C3H5、n-C5H11、n-C16H33)。用电子轰击电离质谱(EI-MS)和核磁共振谱图(^1H-NMR)鉴定了AMQ,研究了不同取代基对这类化合物EI-MS谱图的影响,分析得到一些裂解规律。结果表明:所有样品谱图中均有芳香化合物的特征CnHn^ 系列峰m/z78,65,52,39和(或)m/z77、76、64、63、51、50、38、37。对于末取代的样品及低级烷烃取代的样品,谱图中的基峰为分子离子峰,对于取代基中碳数大于等于3的样品。谱图中的基峰不是分子离子峰,分子离子峰强度随着碳数的增加而降低。这些样品一般容易发生骨架重排,丢失一分子CO,生成1-烷基-2-甲基苯并哒唑正离子。此外,还讨论了谱图中其它的一些碎片离子峰。这对于研究和指导喹喔啉衍生物 的合成,探讨它们在药效及结构特征与生理活性的关系等方面具有重要的应用价值和理论意义。 相似文献
999.
Huang X Margulis CJ Li Y Berne BJ 《Journal of the American Chemical Society》2005,127(50):17842-17851
When supercritical CO2 is dissolved in an ionic liquid, its partial molar volume is much smaller than that observed in most other solvents. In this article we explore in atomistic detail and explain in an intuitive way the peculiar volumetric behavior experimentally observed when supercritical CO2 is dissolved in 1-butyl-3-methylimidazolium hexafluorophosphate ([Bmim+] [PF6(-)]). We also provide physical insight into the structure and dynamics occurring across the boundary of the CO2 ionic liquid interface. We find that the liquid structure of [Bmim+] [PF6(-)] in the presence of CO2 is nearly identical to that in the neat ionic liquid (IL) even at fairly large mole fractions of CO2. Our simulations indicate, in agreement with experiments, that partial miscibilities of one fluid into the other are very unsymmetrical, CO2 being highly soluble in the ionic liquid phase while the ionic liquid is highly insoluble in the CO2 phase. We interpret our results in terms of the size and shape of spontaneously forming cavities in the ionic liquid phase, and we propose that CO2 occupies extremely well-defined locations in the IL. Even though our accurate prediction of cavity sizes in the neat IL indicates that these cavities are small compared with the van der Waals radius of a single carbon or oxygen atom, CO2 appears to occupy a space that was for the most part a priori "empty". 相似文献
1000.
Zhang H Zhou Y Zhang M Shen T Li Y Zhu D 《Journal of colloid and interface science》2002,251(2):443-446
A dyad-anthraquinone-methyl ester of fluorescein-and its model compound-butyl ester-were synthesized. The effects of photo-induced electron transfer from fluorescein to an organic anthraquinone acceptor and injection into inorganic colloidal TiO(2) were studied respectively. It is found that the photo-induced electron transferring to an organic acceptor is much faster than injecting into inorganic colloidal particles when fluorescein was excited by visible light. While inorganic colloidal TiO(2) was excited by UV, the electron of fluorescein will inject into TiO(2). 相似文献