全文获取类型
收费全文 | 4453篇 |
免费 | 226篇 |
国内免费 | 837篇 |
专业分类
化学 | 4588篇 |
晶体学 | 81篇 |
力学 | 135篇 |
综合类 | 54篇 |
数学 | 311篇 |
物理学 | 347篇 |
出版年
2024年 | 4篇 |
2023年 | 61篇 |
2022年 | 92篇 |
2021年 | 76篇 |
2020年 | 161篇 |
2019年 | 175篇 |
2018年 | 185篇 |
2017年 | 176篇 |
2016年 | 190篇 |
2015年 | 146篇 |
2014年 | 190篇 |
2013年 | 438篇 |
2012年 | 506篇 |
2011年 | 240篇 |
2010年 | 196篇 |
2009年 | 239篇 |
2008年 | 289篇 |
2007年 | 293篇 |
2006年 | 253篇 |
2005年 | 226篇 |
2004年 | 211篇 |
2003年 | 176篇 |
2002年 | 144篇 |
2001年 | 97篇 |
2000年 | 124篇 |
1999年 | 104篇 |
1998年 | 92篇 |
1997年 | 72篇 |
1996年 | 66篇 |
1995年 | 47篇 |
1994年 | 40篇 |
1993年 | 23篇 |
1992年 | 49篇 |
1991年 | 25篇 |
1990年 | 28篇 |
1989年 | 19篇 |
1988年 | 15篇 |
1987年 | 6篇 |
1986年 | 6篇 |
1985年 | 5篇 |
1984年 | 7篇 |
1983年 | 5篇 |
1982年 | 3篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 3篇 |
1978年 | 3篇 |
1973年 | 2篇 |
排序方式: 共有5516条查询结果,搜索用时 15 毫秒
1.
By extracting combinatorial structures in well-solved nonlinear combinatorial optimization problems, Murota (1996,1998) introduced the concepts of M-convexity and L-convexity to functions defined over the integer lattice. Recently, Murota–Shioura (2000, 2001) extended these concepts to polyhedral convex functions and quadratic functions in continuous variables. In this paper, we consider a further extension to more general convex functions defined over the real space, and provide a proof for the conjugacy relationship between general M-convex and L-convex functions.Mathematics Subject Classification (1991): 90C10, 90C25, 90C27, 90C35This work is supported by Grant-in-Aid of the Ministry of Education, Culture, Sports, Science and Technology of Japan 相似文献
2.
n进制中非零数字之积函数的均值公式 总被引:8,自引:0,他引:8
设 N =a1nk1+ a2 nk2 +… + asnks( 1 aik2 >… >ks 0 ) ,a( N,n) =a1a2 … as,本文给出了均值 Ar( N ,n) =∑m相似文献
3.
4.
R. Pinna F.J.M. Rutten E.F. Smith M.R. Willis M.R.S. McCoustra 《Applied Surface Science》2006,252(19):6672-6675
Time-of-flight secondary ion mass spectrometry (ToF-SIMS) and polarisation-modulation reflection-absorption infrared spectroscopy (PM-RAIRS) have been used to monitor the surface synthesis of self-assembled aromatic π-conjugated molecular wires on gold substrates as a step towards a novel structure for organic electroluminescent devices (OLEDs). The wires have been synthesised using a series of Schiff's base coupling reactions in solution on a self-assembled monolayer of an aromatic thiolate anchor. ToF-SIMS and PM-RAIRS measurements have demonstrated that: (i) the anchor molecules self-assemble at the gold surface, (ii) the anchor molecules selectively react through imino coupling reactions with additional wire units with high efficiency and (iii) the wire-like structure is predominantly orientated normal to the surface. 相似文献
5.
Hui Zhang 《Journal of solid state chemistry》2004,177(3):772-780
A nano-scale magnetic solid base catalyst MgAl-OH-LDH/MgFe2O4 (where LDH denotes layered double hydroxide) composed of MgAl-OH-LDH Brønsted base catalytic layers coated on MgFe2O4 spinel cores has been prepared. A magnetic precursor MgAl-CO3-LDH/MgFe2O4 was prepared by a method involving separate nucleation and aging steps, and subsequently calcined to give a mixed metal oxide composite MgAl(O)/MgFe2O4 which was rehydrated to give MgAl-OH-LDH/MgFe2O4. The structure and magnetic properties of the nano-scale magnetic solid base MgAl-OH-LDH/MgFe2O4, together with those of the magnetic precursor MgAl-CO3-LDH/MgFe2O4 and MgFe2O4 were characterized by XRD, XPS, low temperature N2 adsorption and vibrating sample magnetometry (VSM). The MgAl-OH-LDH/MgFe2O4 composite possesses a mesoporous structure with pore size ranging from 2 to 20 nm with particle size mainly in the range 35-130 nm. The catalytic properties of MgAl-OH-LDH/MgFe2O4 were evaluated using the self-condensation of acetone at 273 K as a probe reaction. The results showed that the conversion of acetone to diacetone alcohol reached the thermodynamic equilibrium value of 23% at 273 K. The catalyst was easily recovered through application of an external magnetic field, and when the reclaimed catalyst was used in a second run for the same reaction, the reactivity remained unchanged. 相似文献
6.
《Magnetic resonance in chemistry : MRC》2003,41(1):61-64
Palladium(II) dichloride reacts with 1,10‐bis(2‐pyrrolyl)‐2,5,9‐triaza‐1,9‐decadiene to give a [Pd(C15H20N5)]Cl complex in which the ligand is four‐coordinated, leaving one pyrrole group dangling. By using COSY, gHSQC, gHMBC connectivities and NOE experiments it has been concluded that one linkage isomer exists in DMSO solution, in spite of the fact that different sets of N atoms of potentially pentadentate ligand might be involved in coordination, and that the three chelate rings in the complex cation are arranged in a sequence: five‐membered, six‐membered, five‐membered which is different from that (5–5–6) found by x‐ray studies on the related [Ni(C15H20N5)]Cl compound. NMR studies allowed an unambiguous assignment of all 1H and 13C NMR resonances for the complex. Results of x‐ray structural analysis of [Pd(C15H20N5)](CH3COO)H2O supported the five‐membered, six‐membered, five‐membered ring sequence in the [Pd(C15H20N5)]+ complex cation and show an E (trans) orientation of the dangling pyrrole group with respect to the metal center. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
7.
A. Filarowski A. Koll A. Kochel J. Kalenik P. E. Hansen 《Journal of Molecular Structure》2004,700(1-3):67-72
The crystal structures of two ortho-hydroxy ketones (5-chloro-2-hydroxyacetophenone (I K) and 3,5-dichloro-2-hydroxyacetophenone (II K)) have been determined with X-ray diffraction at 100 K. A comparison of steric effects on properties of pseudoaromatic hydrogen bonds in ortho-hydroxy acetophenone and ortho-hydroxy ketimines have been carried out with the application of crystallographic data.
Nuclear quadrupole resonance (NQR) spectra have been measured and interpreted. 相似文献
8.
A simple and rapid method is developed to determine the high acidity and the basicity of solutions by chronopotentiometry with a platinum working electrode. The acidity range from 5.0 mol/l H+ to 1.0 mol/l OH− can be measured by the adjustment of deposition potential and time. The response mechanism to acidity and basicity has been explored. The transition potential plateau in chronopotentiograms is caused from the oxidation of hydrogen adsorbed on electrode surface. 相似文献
9.
Huadong Tang Maciej Radosz Youqing Shen 《Journal of polymer science. Part A, Polymer chemistry》2006,44(22):6607-6615
Uracil‐derivatized monomer 6‐undecyl‐1‐(4‐vinylbenzyl)uracil and diaminopyrimidine‐derivatized monomer 2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine (DMP) were synthesized and polymerized by atom transfer radical polymerization (ATRP). A well‐defined, highly soluble, uracil‐containing polymer, poly[6‐undecyl‐1‐(4‐vinylbenzyl)uracil] (PUVU), was prepared in dioxane at 90 °C with CuBr/1,1,4,7,10,10‐hexamethyltriethylenetetramine as the catalyst and methyl α‐bromophenylacetate as the initiator. PUVU was further used as a template for the ATRP of DMP. The enhanced apparent rate constant of the DMP polymerization in the presence of PUVU indicated that the ATRP of DMP occurred along the PUVU template. The template polymerization produced a stable and insoluble macromolecular complex, PUVU/poly(2,6‐dioctanoylamido‐4‐methacryloyloxypyrimidine). An X‐ray diffraction study confirmed that the complex had strandlike domains. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6607–6615, 2006 相似文献
10.