全文获取类型
收费全文 | 4510篇 |
免费 | 770篇 |
国内免费 | 620篇 |
专业分类
化学 | 1914篇 |
晶体学 | 48篇 |
力学 | 513篇 |
综合类 | 44篇 |
数学 | 730篇 |
物理学 | 2651篇 |
出版年
2024年 | 16篇 |
2023年 | 50篇 |
2022年 | 125篇 |
2021年 | 122篇 |
2020年 | 169篇 |
2019年 | 124篇 |
2018年 | 149篇 |
2017年 | 172篇 |
2016年 | 197篇 |
2015年 | 170篇 |
2014年 | 218篇 |
2013年 | 330篇 |
2012年 | 264篇 |
2011年 | 286篇 |
2010年 | 247篇 |
2009年 | 286篇 |
2008年 | 267篇 |
2007年 | 326篇 |
2006年 | 267篇 |
2005年 | 247篇 |
2004年 | 233篇 |
2003年 | 214篇 |
2002年 | 203篇 |
2001年 | 190篇 |
2000年 | 152篇 |
1999年 | 111篇 |
1998年 | 113篇 |
1997年 | 113篇 |
1996年 | 95篇 |
1995年 | 54篇 |
1994年 | 58篇 |
1993年 | 47篇 |
1992年 | 43篇 |
1991年 | 40篇 |
1990年 | 30篇 |
1989年 | 25篇 |
1988年 | 27篇 |
1987年 | 26篇 |
1986年 | 12篇 |
1985年 | 20篇 |
1984年 | 21篇 |
1983年 | 8篇 |
1982年 | 10篇 |
1981年 | 2篇 |
1980年 | 4篇 |
1979年 | 4篇 |
1978年 | 4篇 |
1977年 | 5篇 |
1973年 | 2篇 |
1957年 | 1篇 |
排序方式: 共有5900条查询结果,搜索用时 0 毫秒
71.
根据氯离子型层状复合氢氧化物(LDH-Cl)制备过程中溶液浓度变化的监测结果和不同反应进程时产物的EDS、IR、XRD、TEM、TG-DTA表征结果,研究了合成LDH-Cl的共沉淀反应动力学特征及机理.实验结果表明, LDH-Cl的生成符合多核层表面反应动力学模型;反应过程中LDH的晶胞参数c从2.421 nm变为2.399 nm,通道高度h由0.3321 nm减小为0.3228 nm,粒子直径Da由6.40 nm增大为15.16 nm, Dc由7.43 nm增大到10.93 nm,纵横比由0.86增大为1.39; IR和TG-DTA特征变化表明了层板对阴离子作用的强度和层板的结构稳定性随反应进程而提高. 相似文献
72.
采用某些特殊的放电和提取方法,如反向放电和甲苯高温高压提取等可以有效地提高稀土富勒烯的生成效率[‘,‘’,并已先后成功高效地合成了许多含稀土富勒烯「‘’.对其提纯、表征、衍生和应用也进行了研究[‘-’j.但对影响稀土富勒烯生成的因素研究较少.在石墨律中同时填入La,Y,Sc的稀土氧化物,对其稀土富勒烯生成效率的情况进行了研究,认为稀土元素的第一电离能是影响稀土富勒烯生成的主要因素‘’,’‘.Moro等采用激光和热解吸质谱对稀土富勒烯的研究结果表明,稀土元素的氧化态是影响稀土富勒烯生成的决定性因素”’.本… 相似文献
73.
多电解质溶液中带电胶体粒子的电势分布由球形Poisson-Boltzmann方程(PBE)描述.PBE是一个非线性的微分方程,且难以求得其解析解.本文采用非线性P-B积分方程,计算电势分布的数值解.首先,根据静电场和热力学系统中的物理定理,导出描述电势分布的P-B积分方程(PBIE);其次,用迭代方法求PBIE的数值解.最后,计算了在3-1型电解液中无量纲半径κa分别为0.12和0.22,无量纲表面电势ξ分别为1,2,4,6时球形胶体粒子外部的电势值.为了检验数值解的精度,计算了表面电荷密度,并与Loeb(1961)和Oshima(1995)等人的结果比较,本文结果的相对误差小于1%,优于Oshima的结果. 相似文献
74.
无机层状复合氢氧化物中顺铂-DNA模型分子的选择性插入 总被引:5,自引:0,他引:5
药物分子的选择性包裹和控制释放是药物研究领域中具有挑战性的研究方向。本文研究表明:顺铂-DNA模型分子cis-[Pt(NH3)2(5′-GMP)2](5′-GMP 5′-单磷酸鸟苷)可插入无机层状复合氢氧化物[Zn0.68Al0.32(OH)2](NO3)0.32·mH2O。但另一种层状复合氢氧化物[LiAl2(OH)6]Cl·H2O由于其阳离子层中正电荷密度较高、阳离子层与层间阴离子之间静电作用较强,因而顺铂-DNA模型分子不能通过离子交换方式插入其层间。光谱数据证实插入层间的顺铂-DNA模型分子结构不变。这可能为铂-DNA分子的传递提供新的方法。 相似文献
75.
The effect of Ni substitution for Mn on magnetic and transport properties has been investigated for layered manganese oxides LaSr2Mn2-xNixO7. Nickel doping hampered the canted antiferromagnetic (AFM) exchange at low temperature and their Neel temperature (TN) decreased from 138 K (x=0) to 102 K (x=0.3). Meanwhile, spin glass, charge ordering and metal-insulator transition are suppressed by Ni addition. The resistivity increases obviously with increasing x due to double exchange interaction channel broken by Ni2+ addition. The resistivity of all samples in low temperature range fits to the Mott′s variable rang hopping (VRH) model, while it fits to nearest neighbor hopping of small polarons model in high temperature range. 相似文献
76.
Chromium and yttrium-doped magnesium aluminum oxides prepared from layered double hydroxides 总被引:1,自引:0,他引:1
J.M. García-García M.E. Prez-Bernal R.J. Ruano-Casero V. Rives 《Solid State Sciences》2007,9(12):1115-1125
Layered double hydroxides with the hydrotalcite-like structures, containing Mg2+ and Al3+, doped with Cr3+ and Y3+, have been prepared by precipitation at constant pH. The weight percentages of Cr3+ and Y3+ were 1, 2, or 3%, and 0.5 or 1%, respectively. Single phases were obtained in all cases, whose crystallinity decreased as the content in Cr and Y was increased. The solids have been characterised by element chemical analysis, powder X-ray diffraction, thermal analyses (differential, thermogravimetric and programmed reduction), FT-IR and UV–vis spectroscopies; the specific surface areas have been determined from nitrogen adsorption isotherms at −196 °C. Upon calcination at 1200 °C for 5 h in air all solids display a mixed structure (spinel and rock salt for MgO); these solids have also been characterised by these techniques and their chromatic coordinates (CIE – L*a*b*) have been determined. Their pink colour makes these solids suitable for being used as ceramic pigments. 相似文献
77.
FT-IR and Raman spectroscopic study of hydrated rubidium (cesium) borates and alkali double borates 总被引:1,自引:0,他引:1
Zhu Lixia Yue Tao Wang Jiang Gao Shiyang 《Russian Journal of Inorganic Chemistry》2007,52(11):1786-1792
FT-IR and Raman spectra of five hydrated alkali borates and five hydrated alkali double borates have been recorded at room
temperature in the range 400 to 4000 cm−1, and analyzed. Fundamental vibrational modes have been identified and assignments tentatively made in comparison with the
work of Janda and Heller, and Li Jun.
The text was submitted by the authors in English. 相似文献
78.
通过流动相中电解质浓度对毛细管电色谱柱效能的流动相平均线速度的影响,研究了CEC中双电层叠加现象。提出选择合适电解质组成的浓度及在制备色谱柱过程中避免细小和破碎的固定相颗粒进入柱中,以有效地减小双电层叠加作用。 相似文献
79.
Òscar Rubio-Pons Boris Minaev Oleksandr Loboda Hans Ågren 《Theoretical chemistry accounts》2005,113(1):15-27
The phosphorescence spectrum of p-dichlorobenzene has been calculated using multiconfiguration self-consistent-field wave functions and the quadratic response technique. Attention has been paid to the intensity distribution of the singlet–triplet (3B1u1Ag) transition through a number of vibronic subbands. The second order spin–orbit coupling (SOC) contribution to the spin splitting of the 3B1u (3*) state is found to be almost negligible, and the calculations therefore provide a good estimate for the zero-field splitting (ZFS) parameters based only on the electron spin–spin coupling expectation values. Nuclear quadrupole resonance constants for the different Cl isotopes are also calculated to accomplish the ZFS assignment. The electric dipole activity of the spin sublevels in the triplet–singlet transitions to the ground-state vibrational levels is estimated by calculations of derivatives using distorted geometries which are shifted from the equilibrium position along different vibrational modes. A vibrational analysis of the phosphorescence spectrum, based on the SOC-induced mixing of the singlet and triplet states calculated along different vibrational modes, provides reasonable agreement with experimental data.Acknowledgment O. R.-P. would like to thank the European MOLPROP network for support. The authors thank Alexander Baev for fruitful discussions. This work was supported by the Swedish Royal Academy of Science (KVA). 相似文献
80.
The total energy of all π-electrons in a conjugated hydrocarbon (within the framework of HMO approximation) is the sum of the absolute value of all
the eigenvalues of its corresponding graph. In this paper, we consider “double hexagonal chains” as benzenoids constructed
by successive fusions of successive naphthalenes along a zig–zag sequence of triples of edges as appear on opposite sides
of each naphthalene unit. It is shown that if the fusions are such as to give a polyaceacene then the total π-electron energy
is the minimum from among all the double hexagonal chains with the same number of naphthalene units.
相似文献