全文获取类型
收费全文 | 273篇 |
免费 | 11篇 |
国内免费 | 1篇 |
专业分类
化学 | 206篇 |
力学 | 3篇 |
数学 | 38篇 |
物理学 | 38篇 |
出版年
2023年 | 3篇 |
2022年 | 12篇 |
2021年 | 11篇 |
2020年 | 11篇 |
2019年 | 15篇 |
2018年 | 12篇 |
2017年 | 9篇 |
2016年 | 18篇 |
2015年 | 11篇 |
2014年 | 15篇 |
2013年 | 21篇 |
2012年 | 21篇 |
2011年 | 20篇 |
2010年 | 9篇 |
2009年 | 8篇 |
2008年 | 13篇 |
2007年 | 9篇 |
2006年 | 19篇 |
2005年 | 8篇 |
2004年 | 6篇 |
2003年 | 4篇 |
2002年 | 3篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1998年 | 2篇 |
1997年 | 3篇 |
1996年 | 1篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1976年 | 1篇 |
排序方式: 共有285条查询结果,搜索用时 15 毫秒
1.
Journal of Statistical Physics - In this paper, we will study the long time behavior of the simple symmetric exclusion process in the “channel” $$\varLambda _N=[1,N]\cap \mathbb {N}$$... 相似文献
2.
Nguyen Hoa Hong Joe Sakai Ngo Thu Huong Virginie Brizé 《Journal of magnetism and magnetic materials》2006
Laser-ablated Co-doped In2O3 thin films were fabricated under various growth conditions on R-cut Al2O3 and MgO substrates. All Co:In2O3 films are well-crystallized, single phase, and room temperature ferromagnetic. Co atoms were well substituted for In atoms, and their distribution is greatly uniform over the whole thickness of the films. Films grown at 550 °C showed the largest magnetic moment of about 0.5 μB/Co, while films grown at higher temperatures have magnetic moments of one order smaller. The observed ferromagnetism above room temperature in Co:In2O3 thin films has confirmed that doping few percent of magnetic elements such as Co into In2O3 could result in a promising magnetic material. 相似文献
3.
P. Thuéry M. Nierlich Z. Asfari J. Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》1997,27(2):169-178
The crystal structures of a new solvate of the ditopic receptor 1,3-calix[4]-bis-crown-6, Bis-C6, and of 1,3-calix[4]-bis-(benzo-crown-6), Bis-benzoC6, are reported. Bis-C6.3 CH3CN (1) crystallizes in the monoclinic space group P21/n, a = 14.388(3), b = 26.947(8), c = 14.707(4) Å, = 113.19(3)°, V = 5241(5) Å3, Z = 4. Refinement led to a final conventional R value of 0.092 for 2723 reflections. The structure of (1) differs from the previously reported structure of Bis-C6.4 CH3CN by the conformation of one crown either chain. Two acetonitrile molecules are in the close neighbourhood of the crown ether cavities. Bis-benzoC6.3 CH3CN (2) crystallizes in the monoclinic space group P21/c, a = 10.391(4), b = 17.264(11), c = 30.426(9) Å, = 94.62(3)°, V = 5440(7) Å3, Z = 4. Refinement led to a final conventional R value of 0.106 for 2965 reflections. Two acetonitrile molecules are located near the crown ether cavities, as in (1). One of the crown ether conformations is the same as in the binuclear caesium complex of Bis-benzoC6, supporting the hypothesis of a preorganization of this ligand towards the complexation of this ion; the second crown ether chain is partially disordered. 相似文献
4.
An application of a new standardization method for rapid activation mass analysis with registration of the strongly absorbed low-energy gamma radiation is described. This method makes it possible to avoid the use of the time-consuming and laborious method of Internal Standard. 相似文献
5.
Journal of Global Optimization - Improperly efficient solutions in the sense of Geoffrion in linear fractional vector optimization problems with unbounded constraint sets are studied systematically... 相似文献
6.
Pierre Thuéry Nelly Keller Monique Lance Julien-Daniel Vigner Martine Nierlich 《Journal of inclusion phenomena and macrocyclic chemistry》1994,20(1):89-96
The doubly deprotonated form of calix[6]arene, with two protonated triethylamines as counter-ions, crystallizes in the monoclinic system: space groupP21/n,a=8.465(4),b=17.822(8),c=15.182(6) Å,=90.18(4)°,V=2291(2) Å3,Z=2. Refinement led to a final conventionalR value of 0.063 for 1046 reflections. The macrocycle conformation is not apinched cone, usual for freeR-calix[6]arene, but a distorted 1,2,3-alternate cone, since the molecule lies on a symmetry center. Furthermore, one of the torsion angles defined by the methylene bridges is near to zero, which is unusual in calixarene structures.
Supplementary Data relating to this article (atomic coordinates for hydrogen atoms, anisotropic displacement parameters for oxygen and nitrogen atoms, and observed and calculated structure factors) are deposited with the British Library as Supplementary Publication No. SUP 82182 (7 pages). 相似文献
7.
P. Thuéry M. Nierlich C. Bressot V. Lamare J. F. Dozol Z. Asfari J. Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》1995,23(4):305-312
The crystal structures of two binuclear complexes between caesium and 1,3-calix[4]-bis-crowns have been determined. Cs2
Bis-benzoC6(NO3)2. 3CHCl3 (1) in whichBis-benzoC6 is 1,3-calix[4]-bis-benzo-crown-6, crystallizes in the orthorhombic system: space groupPca2
1 a=19.513(10),b=15.382(5),c=23.708(9) Å,V=7116(5) Å3,Z=4. Refinement led to a final conventionalR value of 0.065 for 2321 reflections. The structure of (1) is analogous to those already reported withBis-C6, (in whichBis-C6 is, 1,3-calix[4]-bis-crown-6) and NO
3
–
as a counter-ion. Cs2
Bis-C6(NCS)2 (2) crystallizes in the monoclinic system: space, groupC2 a=36.57(2),b=11.47(1),c=13.65(1) Å, =109.03(5)°.,V=5415(6) Å3,Z=4. Refinement led to a final conventionalR value of 0.063 for 2227 reflections. Compound (2) is made of dimers bridged by a disordered NCS– ion. The crown ether chain conformations are discussed.
Supplementary data relating to this article (atomic coordinates, anisotropic displacement parameters, bond distances and angles and observed and calculated structure factors) are deposited with the British Library as Supplementary Publication No. SUP 82199 (52 pages). 相似文献
8.
Tran Dan Thu 《Annals of Combinatorics》2013,17(4):755-763
The LYMinequality (Lubell, Yamamoto, Meshalkin) is a generalization of Sperner’s theorem for antichains. Kleitman and Harper independently proved that the LYM inequality and the normalized matching property (or local LYM inequality) are equivalent. Many contributions have been proposed to sharpen the LYM inequality. Noticeably, Ahlswede and Zhang lifted the LYM inequality to an identity, called the AZ identity. Thus, one expects that the same sharpening of the local LYM inequality is equivalent to the AZ identity. In this paper, we introduce a local LYM identity which sharpens the local LYM inequality and prove that it is equivalent to the AZ identity. The local LYM identity shows local relationships between components in the AZ identity. 相似文献
9.
E. Herrmann Nguyen Thi Thu Chau O. Navratil G. Ohms L. Beyer 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4)
Abstract The new 1,1-disubstituted 3-diphenoxy(thio)phosphoryl-(thio)ureas, R1R2NC(X)NHP(0Ph)2, HA, with X,Y = O,S, were synthesized by addition of secondary mines to the corresponding P-iso(thio)cyanates. This reaction is reversible if X,Y = S. (PhO)2P(Y)Cl reacts with H2NC(X)NR2 in the presence of an HCl acceptor only if X,Y a 0. Side reactions are observed. Phosphorylated derivatives of biuret were isolated from such a reaction mixture. 相似文献
10.
Abstract The synthesis and crystal structure of the complex formed by the all-cis epimer of C-methylcalix[4]resorcinarene (1) and triethylammonium nitrate are reported. “1.(HNEt+ 3)4. (NO? 3)4(2)”, crystallizes in the monoclinic space group P21/n, a=25.796(2), b=16.6048(11), c=29.5659(10) Å, β=94.636(4)°, V=12623(2) Å3, Z=8. Refinement led to a final conventional R1 value of 0.128 for 12428 reflections and 1473 parameters. The resorcinarene displays the usual bowl-type shape, with four hydroxyl protons involved in intramolecular hydrogen bonds, whereas the remaining four make hydrogen bonds with four bridging nitrate ions, which results in the formation of infinite chains. Those chains are arranged so as to form layers, between which the triethylammonium ions and the remaining nitrate ions are hydrogen-bonded one to another. 相似文献