全文获取类型
收费全文 | 418篇 |
免费 | 13篇 |
国内免费 | 1篇 |
专业分类
化学 | 227篇 |
晶体学 | 2篇 |
力学 | 14篇 |
数学 | 132篇 |
物理学 | 57篇 |
出版年
2019年 | 6篇 |
2017年 | 4篇 |
2016年 | 9篇 |
2015年 | 6篇 |
2014年 | 8篇 |
2013年 | 14篇 |
2012年 | 11篇 |
2011年 | 17篇 |
2010年 | 4篇 |
2008年 | 10篇 |
2007年 | 11篇 |
2006年 | 5篇 |
2005年 | 10篇 |
2004年 | 9篇 |
2003年 | 7篇 |
2002年 | 8篇 |
2001年 | 11篇 |
2000年 | 10篇 |
1999年 | 4篇 |
1998年 | 7篇 |
1997年 | 10篇 |
1996年 | 13篇 |
1995年 | 12篇 |
1994年 | 12篇 |
1993年 | 9篇 |
1992年 | 11篇 |
1991年 | 5篇 |
1990年 | 7篇 |
1989年 | 7篇 |
1988年 | 5篇 |
1987年 | 9篇 |
1986年 | 4篇 |
1985年 | 8篇 |
1984年 | 7篇 |
1983年 | 5篇 |
1982年 | 6篇 |
1981年 | 8篇 |
1980年 | 7篇 |
1979年 | 8篇 |
1978年 | 10篇 |
1977年 | 8篇 |
1976年 | 10篇 |
1975年 | 5篇 |
1974年 | 4篇 |
1972年 | 4篇 |
1971年 | 6篇 |
1970年 | 5篇 |
1969年 | 10篇 |
1968年 | 6篇 |
1962年 | 4篇 |
排序方式: 共有432条查询结果,搜索用时 15 毫秒
91.
Abstract. Sunlight and many types of artificial lighting contain near-UV light (300–400 nm). These wavelengths can enter the eye and are maximally absorbed in the lens due to its chemical composition. The lenses of certain animals develop cataracts from exposure to this light, and changes similar to those that occur in human lenses with certain types of cataracts and with aging are inducible in isolated human lenses. These changes seem to be associated with chemical alterations in the essential amino acid tryptophan either as a part of proteins or in free form. Such changes in tryptophan would result in lens cell toxicity, in increased pigmentation of the lens, and in large aggregates of proteins. The latter two changes would result in losses in the ability of the lens to transmit visible light needed for vision, and the abnormal state called cataract would result. Much more work is needed to prove that near-UV light can accelerate cataractous changes in the lenses of living humans. Studies at the basic chemical level are needed, but population studies would be most essential for the final proof. Many preventive measures could become available, including the use of special types of spectacles and dietary additives. 相似文献
92.
Rajadurai C Ivanova A Enkelmann V Baumgarten M 《The Journal of organic chemistry》2003,68(26):9907-9915
Novel pyridine-based nitronyl nitroxide (NIT) biradicals, 3,5-bis[4-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)phenylethynyl)]pyridine (1) and 2,6-bis[4-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)phenylethynyl)]pyridine (2), and monoradicals, 4-(5-bromopyridine-3-ylethynyl)-1-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)benzene (3), 4-trimethylsilylethynyl-1-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)benzene (4), and 4-trimethylsilylethynyl-1-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)pyridine (5), were synthesized and investigated by ESR and UV-vis spectroscopy. The solution EPR measurements of the biradicals gave well-resolved, nine-line spectra with exact half line spacing as compared to monoradicals (giso = 2.0067) with isotropic line spacing /aN/= 7.36 G. This indicates strong, intramolecular exchange coupling (J > 7 x 10(-4) cm(-1); J/aN > 1) of the biradicals with in the limit of EPR. The temperature dependence on the Deltams = +/-2 signal intensity of biradicals follow Curie behavior down to 4 K ascertaining the triplet ground state or its near-degeneracy with the singlet state. UV-vis studies of 1-5 show characteristic differences in the extinctions of n-pi transitions around 600 nm. Both biradicals 1 and 2 were crystallized in monoclinic space groups C2/c and P2(1)/a with the intraradical distances 1.54 and 1.47 nm, respectively. Computational studies of the biradicals 1, 2, and 1,3-bis[4-(1-oxyl-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)phenylethynyl)]benzene (T) were performed by the AM1/CAS(8,8) method to calculate the singlet-triplet (DeltaEST) energy difference and the spin density distribution. Results show that the position of the pyridyl nitrogen in 1 and 2 in comparison with T does not alter the triplet ground-state spin multiplicities supporting the obtained experimental results. 相似文献
93.
[structure: see text] Synthesis and UV-vis, IR, and EPR spectroscopic characterizations, together with X-ray structural analysis, of functional nitronyl- and iminonitroxides attached to pyrazolylbipyridine are described. The exchange interactions between the nitronylnitroxides are found to be stronger than for the iminonitroxides. Although the substitution of a pyridine with the pyrazole ring leads to shorter distances and larger dipolar couplings, the exchange interaction is diminished. While compound 1 forms dimers in the solid state, the terpyridine 3 leads to supramolecular pi-stacking. 相似文献
94.
Norman H. Cromwell Paul B. Woller Henry E. Baumgarten Richard G. Parker David L. Von Minden 《Journal of heterocyclic chemistry》1972,9(3):587-607
The mass spectra of cis-trans isomeric aroylaziridines are presented. Attempts to extend the method for distinguishing between cis and trans isomers previously established for aroylazetidines are described and the results rationalized. A simple fission of the 1-alkylnitrogen bond is described and detailed fragmentation mechanisms are presented and discussed. 相似文献
95.
Bernhardt S Baumgarten M Wagner M Müllen K 《Journal of the American Chemical Society》2005,127(35):12392-12399
Polyphenylene dendrimers possessing a defined number of keto groups in the dendritic scaffold have been synthesized by using a benzophenone-functionalized tetraphenylcyclopentadienone branching unit. A postsynthetic functionalization of the polyphenylene backbone was achieved by reacting the entrapped keto groups with organolithium reagents yielding monodisperse alcohol products. To investigate the accessibility and reactivity of the embedded groups, many functions of different size and nature, for example, the chromophore pyrene, were introduced. Moreover, suitable precursors for the synthesis of dendrimer entrapped species, trityl cations, trityl radicals, and ketyl radical anions, were obtained. To gain insight into the structure of these newly functionalized dendrimers, UV/vis, EPR, and NMR measurements have been performed. They showed a delocalization of the charge/spin into the polyphenylene dendritic arms leading to a stabilization of the ions/radicals. Remarkably, for the ketyl radicals, EPR measurements indicated the occurrence of intermolecular metal-bridged biradicals. They suggest the existence of a dendritic radical network of the dendrimers themselves. 相似文献
96.
97.
98.
Maria Chudnovsky Paul Seymour Sophie Spirkl Mingxian Zhong 《Discrete Mathematics》2018,341(8):2179-2196
The graphs with no five-vertex induced path are still not understood. But in the triangle-free case, we can do this and one better; we give an explicit construction for all triangle-free graphs with no six-vertex induced path. Here are three examples: the 16-vertex Clebsch graph, the graph obtained from an 8-cycle by making opposite vertices adjacent, and the graph obtained from a complete bipartite graph by subdividing a perfect matching. We show that every connected triangle-free graph with no six-vertex induced path is an induced subgraph of one of these three (modulo some twinning and duplication). 相似文献
99.
Given k pairs of vertices (si,ti)(1≤i≤k) of a digraph G, how can we test whether there exist k vertex-disjoint directed paths from si to ti for 1≤i≤k? This is NP-complete in general digraphs, even for k=2 [2], but for k=2 there is a polynomial-time algorithm when G is a tournament (or more generally, a semicomplete digraph), due to Bang-Jensen and Thomassen [1]. Here we prove that for all fixed k there is a polynomial-time algorithm to solve the problem when G is semicomplete. 相似文献
100.
Seymour JL Costello CE Zaia J 《Journal of the American Society for Mass Spectrometry》2006,17(6):844-854
For the analysis of native glycans using tandem mass spectrometry (MS), it is desirable to choose conditions whereby abundances of cross-ring cleavages indicative of branch positions are maximized. Recently, negative ion tandem mass spectrometry has been shown to produce significantly higher abundances of such ions in glycans compared to the positive ion mode. Much of this prior work has concerned fragmentation patterns in asialo glycans. The present work compares the abundances of critical cross-ring cleavage ions using negative mode tandem mass spectrometry for milk oligosaccharides and N-linked glycans. For comparison, product ion formation was studied for deprotonated and nitrated ions formed from asialo glycans and deprotonated ions from sialylated glycans. Breakdown profiles demonstrate clearly that more energy was required to fragment sialylated compounds to the same extent as either their asialo or nitrate adducted counterparts. The extraction of a proton from a ring hydroxyl group during the ionization process may be viewed, qualitatively, as imparting significantly more energy to the ion than would that from a molecule bearing an acidic group, so that acidic glycans are more stable in the gas phase, as the negative charge resides on the carboxyl group. These results have strong practical implications because a major portion of glycans released from mammalian proteins will be sialylated. 相似文献