全文获取类型
收费全文 | 602篇 |
免费 | 23篇 |
国内免费 | 5篇 |
专业分类
化学 | 302篇 |
晶体学 | 3篇 |
力学 | 13篇 |
数学 | 168篇 |
物理学 | 144篇 |
出版年
2022年 | 3篇 |
2021年 | 12篇 |
2020年 | 11篇 |
2019年 | 6篇 |
2018年 | 16篇 |
2017年 | 6篇 |
2016年 | 9篇 |
2015年 | 19篇 |
2014年 | 11篇 |
2013年 | 31篇 |
2012年 | 30篇 |
2011年 | 44篇 |
2010年 | 23篇 |
2009年 | 19篇 |
2008年 | 37篇 |
2007年 | 21篇 |
2006年 | 44篇 |
2005年 | 30篇 |
2004年 | 20篇 |
2003年 | 22篇 |
2002年 | 21篇 |
2001年 | 10篇 |
2000年 | 12篇 |
1998年 | 7篇 |
1997年 | 9篇 |
1996年 | 10篇 |
1994年 | 6篇 |
1993年 | 11篇 |
1992年 | 9篇 |
1991年 | 2篇 |
1990年 | 6篇 |
1989年 | 3篇 |
1988年 | 8篇 |
1987年 | 7篇 |
1986年 | 5篇 |
1985年 | 6篇 |
1984年 | 8篇 |
1983年 | 11篇 |
1982年 | 6篇 |
1981年 | 3篇 |
1980年 | 6篇 |
1979年 | 13篇 |
1978年 | 8篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1975年 | 3篇 |
1974年 | 4篇 |
1973年 | 6篇 |
1972年 | 3篇 |
1971年 | 2篇 |
排序方式: 共有630条查询结果,搜索用时 578 毫秒
131.
Both authors were supported in part by the NSF 相似文献
132.
Specific solvation of nitrated phenoxide, anilide and benzyl anions is shown to decrease in that order, with concomitant increases in substituent salvation assisted resonance effects — the nitrobenzyl anions are suggested to be essentially charge-delocalized. 相似文献
133.
Improved empirical techniques are described for determining the solution structures (coordination numbers and ligand donor groups) of oxoV(IV) complexes from isotropic EPR parameters. These methods will enable more detailed structural information to be obtained than was available previously from such empirical correlations. Assignments of the structures of the V(IV)/oxalate complexes were found to differ from those proposed in the literature and have been important in developing the empirical parameters reported here. In acidic solutions (pH≤1), V(V) oxalate complexes decay slowly to yield three V(IV) complexes, [V(O)(ox)2]2?, [V(O)(ox)(OH2)3]0 andcis-[V(O)(ox)2(OH2)]2? (ox=oxalato(2-)), which have been characterized by EPR spectroscopy. These same three complexes are obtained from the direct reaction of V(IV) with oxalic acid. The structures of these complexes were assigned on the basis of the pH and [oxH2] dependences of the EPR signals and differ significantly to those reported in the literature. The equilibria among the five- and six-coordinate complexes, and the protonation/deprotonation equilibrium of the six-coordinate species are consistent with the well-studied isoelectronic Cr(V) system. 相似文献
134.
A reservoir-type controlled release device based on aqueous-organic partitioning is described. The reservoir is bounded by a microporous or porous membrane, either a hollow fiber or a flat film. The agent partitions between phases at the aqueous-organic interface of the reservoir and the pore mouth, and then diffuses through the membrane pore into a surrounding aqueous solution. The partition coefficient significantly influences the rate of release of the agent. The performance of the system is evaluated using model agents. Controlled release from a reservoir containing a pure organic liquid agent is demonstrated using toluene. Zero-order release is achieved for benzoic acid partitioning from an organic reservoir into water-filled pores, and for nicotine partitioning from an aqueous reservoir into organic-filled pores. Studies using benzoic acid demonstrate the effectiveness of a thin, nonporous coating on slowing the rate of release. A fast-dissolving suspension of benzoic acid in decanol extends the duration of zero-order release. Two agents, nicotine and caffeine, are released simultaneously and independently from a divided reservoir. A simplified mathematical model is presented, and experimental results compared well with those predicted by the model. 相似文献
135.
A negative-ion chemical ionization gas chromatographic-mass spectrometric method for the determination of valproic acid (VPA) and fourteen of its metabolites in a single chromatographic run is reported. The assay features the use of four internal standards and is applicable to the analysis of small serum and urine volumes. A combination of pentafluorobenzyl and trimethylsilyl derivatization resulted in the [M - 181]- ion as the base peak for all the metabolites measured. When these ions were monitored sensitivities in the low picogram levels were achieved. The VPA metabolite profile was determined in pediatric patients on VPA monotherapy and on combined VPA therapy with either carbamazepine or clobazam. The recently characterized diene metabolite, (E,E)-2,3'-diene-VPA, was found to be a major serum metabolite of VPA. In the patient groups taking VPA in combination with carbamazepine, the induction of omega and omega-1 pathways of VPA metabolism was apparent, while the levels of the beta-oxidation products were significantly decreased. 相似文献
136.
The main result is a control theorem for the structure space of E with control near the leaves F in M, where : E M is a fiber bundle over the Riemannian manifold M having a compact closed manifold for fiber and F is a smooth foliation of M, each leaf of which inherits a flat Riemannian geometry from M. A similar result has been proved by the authors under the assumption that each leaf of F is one-dimensional and the fiber of : E M is homotopy stable.Both authors were supported in part by the National Science Foundations. 相似文献
137.
138.
Queite A. de Paula Jean-Pierre Joly Katalin Selmeczi David E. P. Fonseca Giovanni F. Caramori Nicholas P. Farrell 《Journal of Coordination Chemistry》2018,71(11-13):1894-1909
AbstractTwo copper(II) complexes with tetradentate 1,4-disubstituted-1,2,3-triazole ligands, [CuL(MeCN)](ClO4)2 (1) and [CuL′](ClO4)2 (2), have been prepared and characterized by different techniques, including X-ray structure determination, spectroscopic, and electrochemical measurements, as reported elsewhere. Herein, we report the interactions of these complexes, and corresponding free ligands, with human serum albumin (HSA) verifying their relative thermodynamic stability and differences in binding to this protein. Interactions with HSA were verified by CD measurements monitored at 564?nm, up to stoichiometric ratio 2:1 [Complex]:[protein], according to competitive equilibria involving the insertion of copper at the selective N-terminal metal binding site in HSA, and additionally at a secondary nonselective site. Further interactions of these complexes with L-tryptophan residues, and probable supplementary site(s) for the binding, were followed by fluorescence measurements. Analogous experiments with the free L and L′ indicated much weaker interactions. Protein oxidation damage was observed for both complexes, monitored by carbonyl groups formation in the presence of H2O2, probably with the participation of reactive oxygen species. Density functional theory calculations exhibit metal-ligand binding interaction energies similar to [Cu(HSA-Nterminal)]+, and reinforced the experimental results, showing clearly that such triazole ligands are competitive toward copper(II) in biological medium. 相似文献
139.
For every dimension 11, we show the existence of non-homeomorphicharmonic homotopy equivalences, where the target manifold hasnegative curvature. 相似文献
140.
This paper gives a proof of a conjecture of W.-C. Hsiang for the negativeK-theory of integral grouprings , when the group is a subgroup of a uniform lattice in a Lie group. The authors' earlier paper reduced this result to the very special cases where either is finite or is virtually infinite cyclic. The finite case was done much earlier by Carter extending results of Bass and Murthy. The major work of the present paper consists of proving the conjecture when is virtually infinite cyclic.Both authors were supported in part by the National Science Foundation. 相似文献