全文获取类型
收费全文 | 73690篇 |
免费 | 6413篇 |
国内免费 | 4690篇 |
专业分类
化学 | 22917篇 |
晶体学 | 593篇 |
力学 | 4538篇 |
综合类 | 680篇 |
数学 | 13319篇 |
物理学 | 23404篇 |
无线电 | 19342篇 |
出版年
2024年 | 151篇 |
2023年 | 770篇 |
2022年 | 1347篇 |
2021年 | 1691篇 |
2020年 | 1757篇 |
2019年 | 1578篇 |
2018年 | 1444篇 |
2017年 | 1867篇 |
2016年 | 2316篇 |
2015年 | 1924篇 |
2014年 | 3264篇 |
2013年 | 4620篇 |
2012年 | 3707篇 |
2011年 | 3834篇 |
2010年 | 3012篇 |
2009年 | 4201篇 |
2008年 | 4756篇 |
2007年 | 5265篇 |
2006年 | 4385篇 |
2005年 | 3592篇 |
2004年 | 3116篇 |
2003年 | 3293篇 |
2002年 | 3380篇 |
2001年 | 2599篇 |
2000年 | 2432篇 |
1999年 | 2044篇 |
1998年 | 1933篇 |
1997年 | 1243篇 |
1996年 | 1166篇 |
1995年 | 1008篇 |
1994年 | 1013篇 |
1993年 | 783篇 |
1992年 | 867篇 |
1991年 | 587篇 |
1990年 | 543篇 |
1989年 | 404篇 |
1988年 | 346篇 |
1987年 | 316篇 |
1986年 | 285篇 |
1985年 | 256篇 |
1984年 | 257篇 |
1983年 | 163篇 |
1982年 | 218篇 |
1981年 | 206篇 |
1980年 | 133篇 |
1979年 | 170篇 |
1978年 | 141篇 |
1977年 | 125篇 |
1976年 | 84篇 |
1973年 | 59篇 |
排序方式: 共有10000条查询结果,搜索用时 78 毫秒
991.
Excess volumes V
E
of binary liquid mixtures of quinoline with alkanols have been determined from densities at 30°C as a function of composition. The excess volumes are negative over the whole mole fraction range for all the mixtures and decrease with increasing length of alkanol (C1–C10). The VE data have been analyzed in terms of an approach which uses graph theoretical connectivity parameters of the third degrees for two components. The analysis gives information regarding associated species in the pure state and in the mixture. It is suggested that, in the mixture state, no change occurs in the association of alkanols. 相似文献
992.
L. S. Vasil'ev O. G. Azarevich V. S. Bogdanov M. N. Bochkareva V. A. Dorokhov 《Russian Chemical Bulletin》1992,41(11):2104-2107
Boron chelates were obtained by the reaction of butoxy(butylthio)diphenylborane with 5,5,5-trifluoro(trichloro)-4-aminopent-3-en-2-one, and their reactions with primary amines were investigated. -Diiminate complexes of boron with trifluoro- and trichloromethyl groups were synthesized.N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 11, pp. 2657–2661, November, 1992. 相似文献
993.
A series of P[N-isopropylacrylamide (NIPAM)] latexes with different contents of cyano groups were successfully prepared by either seeded
or shot-growth polymerizations of an aqueous solution containing acrylonitrile (AN) onto a seed P[NIPAM] latex, respectively, and further characterized by FT-IR, 1H-NMR, elemental analysis, as well as by quasielastic light scattering (QELS) and scanning electron microscopy (SEM). All
prepared surface-cyanofunctionalized P[NIPAM] latexes exhibited the same range of lower critical solution temperature (LCST) as a pure P[NIPAM] latex. The shot polymerization process proved more efficient at yielding cyano derivatized latexes than the seeded
polymerization technique. The amount of incorporated cyano groups onto the particles was determined with a good correlation
both by 1H-NMR and elemental analysis. The higher the amount of initially introduced AN monomer in the reaction mixture, the more cyano
groups were incorporated onto the particles. The surface of the particles with high content of cyano groups appeared quite
rough by SEM in comparison with that of the pure P[NIPAM] particles.
Received: 25 February 1998 Accepted: 23 June 1998 相似文献
994.
A. N. Kornev O. S. Donnikova V. V. Semenov Yu. A. Kurskii 《Russian Chemical Bulletin》1995,44(1):145-148
A method for preparing (trichloromethyl)organosilanes by the catalytic decarboxylation of the corresponding trichloroacetoxysilanes RMe2SiOC(O)CCl3 (R = Me, ClCH2, Ph, Me3Si, and H) has been developed. The method involves heating the starting compounds without a solvent in the presence of a catalyst (quaternary ammonium salts or potassium salts with the addition of crown ethers). Tertiary amines (Et3N, Bu3N) catalyze this reaction only when heating is carried out in donor aprotic solvents (THF, acetonitrile) in the presence of oxygen. Thermal decomposition of (trichloroacetoxy)organosilanes, in contrast to catalytic decarboxylation, begins at a higher temperature and yields a mixture of products.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 150–153, January, 1995. 相似文献
995.
研究开发的一种新型的元素光度检测器主要用于锗、砷、锡和锑的氢化物气相色谱检测,具有高灵敏,高选择性。它是在普通火焰光度检测器的基础上加装了特制的滤光片改制而成的。对锗、砷、锡和锑的检测限分别为3.0×10 ̄(-11)g、7.0×10 ̄(-11)g、7.0×10 ̄(-10)g和1.1×10 ̄(-8)g,相对标准偏差分别为1.8%、2.4%、2.6%和3.0%。 相似文献
996.
Alkaline-earth (Ae) metals have attracted a wealth of interdependent research from synthetic chemists. In Ae-catalyzed organometallic reactions, β-diketiminate is a typical ligand used to stabilize Ae catalysts by forming six-membered rings comprising Ae metals. Herein, studies focusing on the configuration of β-diketiminate-coordinated Ae compounds observed that the CC and CN bonds are homogeneous and unchanged. Furthermore, energetic studies observed that the formation of the Ae-incorporated six-membered rings results in enhanced stability of >20 kcal/mol. The nucleus-independent chemical shifts, anisotropy of the induced current density, and molecular orbital analyses demonstrated the non-aromaticity of the β-diketiminate-coordinated Ae compounds. The improved stability of these compounds can be explained by the delocalization of the π electrons derived from the β-diketiminate moiety. 相似文献
997.
S. Dirè P. Egger M. L. Di Vona M. Trombetta S. Licoccia 《Journal of Sol-Gel Science and Technology》2004,32(1-3):57-61
The preparation of nanostructured organic-inorganic materials by assembling of nanobuilding blocks allows controlling the extent of phase interaction, which in its turn governs structure-properties relationships. We present here the synthesis of siloxane-based nanobuilding blocks prepared by reacting diphenylsilanediol with vinyltriethoxysilane and triethoxysilane. The reaction products were obtained by non-hydrolytic condensation between silanediol and ethoxide groups in inert atmosphere, in the presence of pyridine, triethylamine or butyl lithium. Different synthetic conditions were examined by means of ATR-FTIR and NMR spectroscopies, showing the formation of siloxane bonds. In the case of triethoxysilane the reaction carried out in the presence of pyridine leads to Si–H bond preservation in the final product. Air stable products with improved Si–O–Si hydrolytic stability can be obtained by removal of the base after the reaction completion. The condensation products can be described as a mixture of siloxane rings involving difunctional and trifunctional silicon units. 相似文献
998.
I. K. Battisha A. El Beyally S. Abd El Mongy A. M. Nahrawi 《Journal of Sol-Gel Science and Technology》2007,41(2):129-137
Structural characteristics of pure silica gel (silica-xerogel, SiO2) and silica gel doped with some rare earth elements (REEs) such as, praseodymium Pr3+, and Europium Eu3+, Erbium Er3+ and Holmium Ho3+ ions, with different concentrations ranging from 1 up to 6%, in the form of monolith materials were prepared by sol-gel technique,
Using tetra-ethoxysilane as precursor materials, which are of particular interest for sol-gel integrated optics applications.
Some structural features of sol-gel derived monolith are analyzed, namely the structure of nano-particle momolith samples,
based on X-ray diffraction (XRD) and Fourier Transform Infrared (FTIR). We show that the XRD spectra of α-crystobalite are
obtained for the pure samples at 1100°C and even by doping with the four REEs ions. 相似文献
999.
Conversion reactions of n-butenes over zeolites and amorphous catalysts have been investigated to deduce the factor that determines the selectivity
for the skeletal isomerization producing isobutene. The effects of pore structure and acid site concentration on the selectivity
for the skeletal isomerization are discussed on various catalysts. The pore structures of FER and CLI zeolites induce the
distant locations of butene molecules, accelerating monomolecular skeletal isomerization. On the other hand, acid site concentration
determines the preferred reaction path of n-butenes on amorphous catalysts. Oligomerization followed by cracking that produces various hydrocarbons is suppressed on
the catalyst with low acid site concentration, resulting in high selectivity for isobutene. The feasibility of monomolecular
skeletal isomerization on zeolites and amorphous catalysts is confirmed by its reversibility with high selectivity. 相似文献
1000.
TiO2光催化反应及其在环境保护中的应用 总被引:8,自引:0,他引:8
本文简要介绍了TiO2光催化剂的作用机理,讨论了影响TiO2光催化效率的因素及解决途径,综述了光催化在环境保护中的最新应用。 相似文献