全文获取类型
收费全文 | 666篇 |
免费 | 20篇 |
国内免费 | 9篇 |
专业分类
化学 | 448篇 |
晶体学 | 2篇 |
力学 | 11篇 |
数学 | 114篇 |
物理学 | 120篇 |
出版年
2023年 | 4篇 |
2022年 | 6篇 |
2021年 | 17篇 |
2020年 | 13篇 |
2019年 | 9篇 |
2018年 | 8篇 |
2017年 | 6篇 |
2016年 | 13篇 |
2015年 | 20篇 |
2014年 | 15篇 |
2013年 | 37篇 |
2012年 | 20篇 |
2011年 | 43篇 |
2010年 | 19篇 |
2009年 | 20篇 |
2008年 | 36篇 |
2007年 | 26篇 |
2006年 | 33篇 |
2005年 | 33篇 |
2004年 | 31篇 |
2003年 | 24篇 |
2002年 | 24篇 |
2001年 | 16篇 |
2000年 | 16篇 |
1999年 | 7篇 |
1998年 | 6篇 |
1997年 | 12篇 |
1996年 | 9篇 |
1995年 | 6篇 |
1994年 | 7篇 |
1993年 | 15篇 |
1992年 | 10篇 |
1991年 | 6篇 |
1990年 | 7篇 |
1989年 | 5篇 |
1988年 | 6篇 |
1987年 | 5篇 |
1986年 | 11篇 |
1985年 | 9篇 |
1984年 | 12篇 |
1983年 | 9篇 |
1982年 | 10篇 |
1981年 | 3篇 |
1980年 | 14篇 |
1979年 | 5篇 |
1978年 | 7篇 |
1976年 | 4篇 |
1974年 | 4篇 |
1970年 | 3篇 |
1898年 | 2篇 |
排序方式: 共有695条查询结果,搜索用时 31 毫秒
1.
da Silva Andre Luis Ferreira Salas Ruben Andres Silva Emilio Carlos Nelli 《Meccanica》2021,56(2):417-437
Meccanica - Fiber reinforced materials are used in assorted engineering application and for this reason, new additive manufacturing technologies have been developed for this type of materials. With... 相似文献
2.
Mariana Weissmann Andres Saul 《Physica C: Superconductivity and its Applications》1991,180(5-6):381-386
An alloy model is proposed for the electronic structure of high-temperature superconductors. It is based on the assumption that holes and extra electrons are localized in small copper-oxygen clusters, that would be the components of such an alloy. This model, when used together with quantum chemical calculations on small clusters, can explain the structure observed in the experimental densities of states of both hole and electron superconductors close to the Fermi energy. The main point is the strong dependence of the energy level distribution and composition on the number of electrons in a cluster. The alloy model also suggests a way to correlate Tc with the number of holes, or extra electrons, and the number of adequate clusters to locate them. 相似文献
3.
Jan Andres Karel Pastor Pavla Šnyrychová 《Journal of Fixed Point Theory and Applications》2007,2(1):153-170
A multivalued version of Sharkovskiĭ’s theorem is formulated for M-maps on linear continua and, more generally, for triangular M-maps on a Cartesian product of linear continua. This improves the main result of [AP1] in the sense that our multivalued
analogue holds with at most two exceptions. A further specification requires some additional restrictions. For instance, 3-
orbits of m-maps imply the existence of k-orbits for all
k ? \mathbbNk \in {\mathbb{N}}
, except possibly for
k ?k \in
{4, 6}. It is also shown that, on every connected linearly ordered topological space, an M-map with orbits of all periods can always be constructed. This demonstrates that Baldwin’s classification of linear continua
in terms of admissible periods [Ba] is useless for multivalued maps. 相似文献
4.
The formation of complexes between tin(IV) and o-diphenols, and o-hydroxyquinones, has been studied spectrophotometrically. Simple o-hydroxyquinones do not react with tin(IV), chloranilic acid gives an SnR2 complex, and o-diphenols give SnR3 complexes. The reactions of tin(IV) with hydroxyxanthene dyes to give coloured products were considered for their possible analytical utility: the pH range, absorption spectrum, solubility and composition of the complexes were investigated, and the stability constants determined. Analytical procedures have been developed for tin and checked for precision and sensitivity: gallein and hydroxyhydroquinonephthalein (dihydroxyfluorescein) are to be recommended. 相似文献
5.
An n-octylmethyl, diphenyl-polysiloxane called SOP-50-Octyl was prepared by a condensation reaction of bis(dimethylamino) n-octylmethylsilane with diphenylsilanediol. The resulting copolymer was a gum with high molecular weight and was obtained with a yield of 80%. 1H and 29Si NMR spectroscopy revealed that the copolymer was a 52% octylmethyl, 48% diphenyl-polysiloxane with random microstructure. Small cyclic impurities could be almost quantitatively removed via a purification step. SOP-50-Octyl was used as stationary phase for the preparation of wall coated open tubular fused silica capillary columns for gas-liquid chromatography. The capillary columns exhibited high separation efficiency and high inertness. The stationary phase offered a unique selectivity due to its unique composition. The Rohrschneider-McReynolds constants indicated a low overall polarity in spite of the high phenyl content, as the polarity was distinctly decreased by the octyl substituent. Furthermore, the octyl substituent was responsible for a high column bleed, reducing the maximum allowable operating temperature to 280 degrees C. The elution temperatures of apolar compounds were increased due to increased interaction of the octyl substituent with the analytes. Some applications with volatile and semi-volatile organic compounds illustrate that SOP-50-Octyl is an excellent choice for confirmational analyses. 相似文献
6.
Daniel Bellu Hanspeter Fischer Hans Greuter Pierre Martin 《Helvetica chimica acta》1978,61(5):1784-1813
Syntheses of Moniliformin, a Mycotoxine with a Cyclobutenedione Structure Six different routes to 3-hydroxy-3-cyclobutene-1, 2-dione ( 4 ), the free acid of the mycotoxine Moniliformin (=alkali salt of 4 ) are described. A common feature of all pathways is the synthesis of cyclobutanes having the oxidation level 6. Moniliformin precursors which are easily transformed to 4 by acid catalysed hydrolysis include [2+2]-cycloadducts of ketene with tetraalkoxy-olefins, 3,4,4-trialkoxycyclobutenes, derivatives of polyfluorinated cyclobutenes, the brominated [2+2]-cycloadduct of ethyl vinyl ether and dichloroketene, tetrabromocyclobutanone, [2+2]-photocycloadducts of dichlorovinylenecarbonate with dichloroethylenes, and the dimer of chloroketene. The most convenient synthesis via the [2+2]-cycloadduct of tetraethoxyethylene and ketene ( 14b ) is reported in detail and produces 4 in four simple steps in 57% overall yield. In addition, two new syntheses of squaric acid ( 56 ) are described. 相似文献
7.
F. Flores P. L. de Andres F. J. Garcia-Vidal L. Jurczyszyn N. Mingo R. Perez 《Progress in Surface Science》1995,48(1-4):27-38
Physisorption on metal surfaces, and the tunneling currents through the adsorbed species, are calculated using a unified formalism that presents both problems on the same footing. Our method is based on a self-consistent LCAO approach whereby the different interaction parameters defining the bonds, and the tunneling currents, are calculated using the atomic properties of the atomic species forming the interface. Green function methods and the Keldish formalism are used to calculate the different physical properties. We present results for xenon adsorbed on aluminum. 相似文献
8.
Wilfredo Hernndez Evgenia Spodine Andres Vega Rainer Richter Jan Griebel Reinhard Kirmse Uwe Schrder Lothar Beyer 《无机化学与普通化学杂志》2004,630(10):1381-1386
The N‐acyl thiourea complexes bis[N,N‐diethyl‐N′‐(p‐nitrobenzoyl)‐thioureato]copper(II) ( 1a,1b ) and bis(N,N‐diphenyl‐N′‐benzoylthioureato)copper(II) ( 2a,2b ) crystallize in each case in two modifications. X‐ray structural analysis shows that 1a and 1b are cis‐trans isomers. This is very unusual for N‐acyl thioureato complexes because with exception of one platinum(II) complex up to now only cis complexes have been found. In contrast X‐ray structural analysis of both forms 2a and 2b of the other complex shows no cis‐trans pair. Both modifications are cis complexes. In solution both isomers of the copper(II) complexes are observable by EPR spectroscopy. 相似文献
9.
On the Reaction of Some 2H-Pyran-2-one Derivatives with Primary Amines The versatile reactivity of 6-unsubstituted 2H-pyran-2-ones towards aliphatic and aromatic amines has been studied. It was found that the result of the reaction depends not only on the substitution of 2H-pyran-2-ones and on the structure of amines, but also on the stoichiometric ratio of reacting compounds. 相似文献
10.
The determination of reaction paths for enzyme systems remains a great challenge for current computational methods. In this paper we present an efficient method for the determination of minimum energy reaction paths with the ab initio quantum mechanical/molecular mechanical approach. Our method is based on an adaptation of the path optimization procedure by Ayala and Schlegel for small molecules in gas phase, the iterative quantum mechanical/molecular mechanical (QM/MM) optimization method developed earlier in our laboratory and the introduction of a new metric defining the distance between different structures in the configuration space. In this method we represent the reaction path by a discrete set of structures. For each structure we partition the atoms into a core set that usually includes the QM subsystem and an environment set that usually includes the MM subsystem. These two sets are optimized iteratively: the core set is optimized to approximate the reaction path while the environment set is optimized to the corresponding energy minimum. In the optimization of the core set of atoms for the reaction path, we introduce a new metric to define the distances between the points on the reaction path, which excludes the soft degrees of freedom from the environment set and includes extra weights on coordinates describing chemical changes. Because the reaction path is represented by discrete structures and the optimization for each can be performed individually with very limited coupling, our method can be executed in a natural and efficient parallelization, with each processor handling one of the structures. We demonstrate the applicability and efficiency of our method by testing it on two systems previously studied by our group, triosephosphate isomerase and 4-oxalocrotonate tautomerase. In both cases the minimum energy paths for both enzymes agree with the previously reported paths. 相似文献