全文获取类型
收费全文 | 585篇 |
免费 | 28篇 |
国内免费 | 9篇 |
专业分类
化学 | 304篇 |
晶体学 | 4篇 |
力学 | 28篇 |
数学 | 179篇 |
物理学 | 107篇 |
出版年
2023年 | 5篇 |
2022年 | 17篇 |
2021年 | 19篇 |
2020年 | 7篇 |
2019年 | 20篇 |
2018年 | 17篇 |
2017年 | 25篇 |
2016年 | 27篇 |
2015年 | 26篇 |
2014年 | 26篇 |
2013年 | 46篇 |
2012年 | 49篇 |
2011年 | 50篇 |
2010年 | 29篇 |
2009年 | 17篇 |
2008年 | 26篇 |
2007年 | 16篇 |
2006年 | 20篇 |
2005年 | 19篇 |
2004年 | 16篇 |
2003年 | 10篇 |
2002年 | 10篇 |
2001年 | 6篇 |
2000年 | 6篇 |
1999年 | 7篇 |
1998年 | 2篇 |
1997年 | 7篇 |
1996年 | 8篇 |
1995年 | 4篇 |
1994年 | 6篇 |
1993年 | 2篇 |
1992年 | 5篇 |
1991年 | 2篇 |
1990年 | 3篇 |
1987年 | 6篇 |
1986年 | 5篇 |
1985年 | 8篇 |
1984年 | 11篇 |
1981年 | 6篇 |
1980年 | 1篇 |
1979年 | 4篇 |
1978年 | 3篇 |
1977年 | 4篇 |
1976年 | 4篇 |
1975年 | 5篇 |
1974年 | 3篇 |
1973年 | 1篇 |
1971年 | 1篇 |
1970年 | 2篇 |
1969年 | 1篇 |
排序方式: 共有622条查询结果,搜索用时 31 毫秒
1.
Khanh Le Chau Pham Duc Chinh 《Zeitschrift für Angewandte Mathematik und Physik (ZAMP)》1991,42(4):614-622
In this paper inequalities for the effective conductivity of isotropic composite materials are derived. These inequalities depend on several coefficients characterizing the microstructure of composites. The obtained coefficients can be exactly calculated for models of a two-component aggregate of multisized, coated ellipsoidal inclusions, packed to fill all space. As a result, new bounds for effective conductivity, considerably narrower than those of Hashin-Shtrikman, are established for such models of composite materials. 相似文献
2.
3.
4.
This review covers our extensive research activities in the area of fluorine containing phospha- and arsaalkenes as well as selenocarbonyls, which differ considerably in their properties and reactivities from their alkyl and aryl counterparts and thus contribute in a gratifying manner to the still growing field of unsaturated element-carbon compounds of 3rd and 4th row main group elements E. Of particular interest is the influence of the fluorine substituents and other small groups (OR, NR2) with either inductive and/or mesomeric effects on the polarity and reactivity of the EC bond. Addition reactions of proton acidic and hydridic polar HX reactants as well as [2+2], [3+2] and [4+2] cycloadditions have been thoroughly studied. The results obtained allow a classification of the EC systems within five different types, A to E, and prove a change from “normal” to “inverse” heteroalkenes in this sequence. The ligand properties of some derivatives have also been investigated in some detail. 相似文献
5.
The kinetics of radical telomerization of VDF at 141 °C, initiated by ditertbutylperoxide, in the presence of three chain transfer agents (CTAs), HCCl3, CCl4 and CCl3Br, are presented. The values of the chain transfer constants were assessed as 35, 0.25 and 0.06 at 141 °C for CCl3Br, CCl4 and HCCl3, respectively. The values of the degree of polymerization (DPn) were obtained for each CTA and were compared for the same CTA concentration. Hence, CCl3Br behaved as an efficient CTA towards VDF and usually afforded the monoadduct selectively, but in certain conditions the VDF diadduct can also be produced. In contrast, HCCl3 was not so efficient since a polymeric structure was identified as the major product. 相似文献
6.
We study a class of quasilinear elliptic equations on the unit ball of ℝ
n
in the divergence form ∑
j=1
n
D
j{G(|x|2,|Du|2)D
j
u} =H(|x|) and get estimates on the boundary by using a modified barrier-function technique of Bernstein. We establish a maximum principle
for the gradients of solutions and get a global gradient estimate. We prove that solutions with constant boundary condition
must be radial. Finally, we apply these results to graphs {(x,u(x)):x∈H
n
} whereu:H
n
→ℝ is a smooth map of then-hyperbolic spaceH
n
=B(0,1) with the metric
to get the existence of graphs with radial prescribed mean curvature. 相似文献
7.
Wilson SR Yurchenko ME Schuster DI Khong A Saunders M 《The Journal of organic chemistry》2000,65(9):2619-2623
Fullerene (C60) Diels-Alder adducts with perfluoroalkylated 1,3-cyclopentadiene (1a,b) were synthesized and studied. The perfluoroalkylated cyclopentadiene was found to be less reactive toward C60 than cyclopentadiene itself, possibly because of the electron-withdrawing effect of the side chain. Because of the same effect, the temperature of the retro-Diels-Alder reaction for the fluorinated adducts was lower (70 degrees C) than the reported value (95 degrees C) for the cyclopentadiene adducts of C60. Higher adducts of the fluorous diene and C60 were found to be soluble in perfluorohexane and to show visible partitioning between organic (toluene) and fluorous phases. Also, the Diels-Alder addition of the fluorous diene was accompanied by extensive oxidation of the fullerene core, as revealed by MALDI-TOF data. 相似文献
8.
S V Dzyadevych T Mai Anh A P Soldatkin N Duc Chien N Jaffrezic-Renault J-M Chovelon 《Bioelectrochemistry (Amsterdam, Netherlands)》2002,55(1-2):79-81
This article describes a biosensor based on pH-sensitive field-effect transistors (pH-FETs) as transducer, and immobilised enzyme tyrosinase as biorecognition element, which was used for the determination of phenolic compounds in water solutions. The biologically active membrane was formed by cross-linking of tyrosinase with bovine serum albumin (BSA) in saturated glutaraldehyde (GA) vapours on the sensitive transducer surface. The main analytical characteristics were studied under different conditions as well as the possibility to optimise these working parameters. Different factors such as the pH of immobilisation, the enzyme loading, the time of exposition to glutaraldehyde vapours were investigated in regards to the influence on sensitivity, limit of detection, dynamic range, and operational and storage stability. 相似文献
9.
10.
Joseph Grobe Duc Le Van Franz Immel Marianne Hegemann Bernt Krebs Mechtild Lge 《无机化学与普通化学杂志》1996,622(1):24-34
Reactive E = C(pp)π-Systems. XLII [1]. Novel Coordination Compounds of 2-(Diisopropylamino)-1-phosphaethyne: [{η4-(iPr2NCP)2}Ni{η2-(iPr2NCP)}], [(Ph3P)2Pt{η2-(iPr2NCP)}], and [Co2(CO)6{η2-μ2-(iPr2NCP)}] 2-(Diisopropylamino)-phosphaethyne iPr2N? C?P ( 2 ) reacts with the Ni(0)-complexes [Ni(1,5-cyclooctadiene)2] and [Ni(CO)3(1-azabicyclo[2.2.2]octane)], respectively, to give the novel complex [{η4-(iPr2NCP)2}Ni{η2-(iPr2NCP)}] ( 5 ), with the 1,3-diphosphacyclobutadiene derivative and 2 (side-on) as π-ligands. The molecular structure of 5 determined by X-ray diffraction on single crystals proves the spin systems and rotational barriers deduced from NMR-data (1H, 13C-, 31P). The PC distances of the four-membered ring of 1.817(2) and 1.818(2) Å – as expected – are considerably longer than the PC bond of the η2-coordinated phosphaalkyne 2 [1.671(2) Å]. – In the reactions of 2 with [(Ph3P)2Pt(C2H4)] or [Co2(CO)8] the ligand properties of 2 resemble those of alkynes affording the complexes [(Ph3P)2Pt{η2-(iPr2NCP)}] ( 7 ) with side-on coordinated 2 and [Co2(CO)6{η2-μ2-(iPr2NCP)}] with 2 acting as a 4e donor bridge in quantitative yield. In attempts to prepare copper(I) complexes of the aminophosphaalkyne 2 by reaction with CuCl or CuI the only isolable product formed in reasonable amounts under the influence of air and moisture is the 1 λ3, 3 λ5-diphosphetene (iPr2N) ( 10 ) (isolated yield: ca. 20%). The crystal structure analysis of 10 indicates a strong structural relationship to the diamino-2-phosphaallyl cation [Me(iPr2N)]+ ( 12 ), the 1,3-diphosphacyclobutadiene ligand (iPr2NCP)2 in the binuclear complex [{η1, μ2-(iPr2NCP)2}Ni2(CO)6] ( 3a ) as well as to the heterocycles (dme)2LiOE2′ (E′ = S, 11a ; E′ = Se, 11b ) prepared by Becker et al. [11b, 35]. 相似文献