全文获取类型
收费全文 | 244篇 |
免费 | 5篇 |
专业分类
化学 | 180篇 |
晶体学 | 2篇 |
力学 | 4篇 |
数学 | 36篇 |
物理学 | 27篇 |
出版年
2023年 | 1篇 |
2022年 | 10篇 |
2021年 | 18篇 |
2020年 | 10篇 |
2019年 | 5篇 |
2018年 | 6篇 |
2017年 | 3篇 |
2016年 | 4篇 |
2015年 | 10篇 |
2014年 | 9篇 |
2013年 | 20篇 |
2012年 | 18篇 |
2011年 | 21篇 |
2010年 | 14篇 |
2009年 | 11篇 |
2008年 | 22篇 |
2007年 | 12篇 |
2006年 | 12篇 |
2005年 | 10篇 |
2004年 | 9篇 |
2003年 | 4篇 |
2002年 | 6篇 |
1999年 | 1篇 |
1998年 | 1篇 |
1997年 | 1篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1983年 | 2篇 |
1982年 | 1篇 |
1979年 | 1篇 |
排序方式: 共有249条查询结果,搜索用时 0 毫秒
241.
Bucşa M Pollnitz A Varga RA Pîrnău A Silvestru A Vlassa M 《Dalton transactions (Cambridge, England : 2003)》2012,41(15):4506-4510
A broadening of the investigation of the ring-chain tautomeric process of N-substituted 1,3-X,N-heterocycles (X = O, S, NR) to Se containing macrocyclic compounds allowed the isolation and structurally solid state characterization of the cyclic tautomer 7, which due to the length of the aliphatic chain, is able to form a stable six-membered ring (6-endo-trig). The theoretical calculations based on the DFT method (Gaussian 03 software package) also support the fact that tautomer 7 is more stable than the chain tautomer 6. Thus, based on the ring-chain tautomerism of the macrocycles that contain alkyl chains with amino-imino, imino-alcohol or sulphur-imino groups, combined with a strategy that allows the formation of a stable six-membered ring, the main reaction products will be the cyclic tautomers. The ring-chain equilibria of these macrocycles could be exploited advantageously in different areas of macrocyclic, physical and medicinal chemistry in order to obtain compounds with practical applications. 相似文献
242.
243.
Saravanakumar S Oprea AI Kindermann MK Jones PG Heinicke J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(11):3143-3154
Two novel anellated N-heterocyclic carbenes (NHC), 1,3-dineopentylnaphtho[2,3-d]imidazol-2-ylidene, and 1,3-dineopentyl-2-ylido-imidazolo[4,5-b]pyridine were obtained by reduction of the respective thiones with potassium, the former also by deprotonation of the corresponding naphthimidazolium hexafluorophosphate by using excess KH in THF. The use of equimolar amounts of KH provided an unexpected formal addition product of this NHC with KOH. X-ray crystal structure analysis of the adduct provided evidence for a distorted tetrameric N-heterocyclic alkoxide, stabilized by two THF molecules. In C(6)D(6) the compound undergoes disproportionation. Transition-metal complexes [(NHC)AgCl], [(NHC)Rh(cod)Cl], and (E)-[(NHC)(2)PdCl(2)] of the novel naphthimidazol-2-ylidene were synthesized. X-ray crystal structures and (1)H and (13)C NMR spectroscopic data provided detailed structural information. Comparing characteristic data with those of nonanellated and differently anellated NHCs or their complexes provides information on the influence of the extended anellation. 相似文献
244.
Bogdan A Rudzevich Y Vysotsky MO Böhmer V 《Chemical communications (Cambridge, England)》2006,(28):2941-2952
Calix[4]arenes bearing at their wide rim four urea residues easily form hydrogen bonded dimeric capsules. This has been used to preorganise alkenyl functions attached to these urea groups for their controlled connection via metathesis reaction. Multimacrocyclic tetraurea derivatives are thus obtained in excellent yields via heterodimers which are formed exclusively with tetratosylurea derivatives. Heterodimerisation of such bis- and tetraloop tetraureas leads analogously to multicatenanes, or to rotaxanes by stoppering. Huge macrocycles are detached from tetraloop derivatives by cleavage of the urea function. 相似文献
245.
Anca Daniela M?cinic 《Topology and its Applications》2009,156(4):761-774
We analyze the monodromy action, over the rationals, on the first homology group of the Milnor fiber, for arbitrary subarrangements of Coxeter arrangements. We propose a combinatorial formula for the monodromy action, involving Aomoto complexes in positive characteristic. We verify the formula, in cases A, B and D. 相似文献
246.
We introduce a new Fenchel dual for vector optimization problems inspired by the form of the Fenchel dual attached to the
scalarized primal multiobjective problem. For the vector primal-dual pair we prove weak and strong duality. Furthermore, we
recall two other Fenchel-type dual problems introduced in the past in the literature, in the vector case, and make a comparison
among all three duals. Moreover, we show that their sets of maximal elements are equal. 相似文献
247.
248.
249.
Silvana Maione Georgina Fabregat Luis J. del Valle Anca‐Dana Bendrea Luminita Cianga Ioan Cianga Francesc Estrany Carlos Alemán 《Journal of Polymer Science.Polymer Physics》2015,53(4):239-252
Graft copolymers formed by anchoring poly(ethylene glycol) (PEG) chains to conjugated polythiophene have been prepared by copolymerizing two compounds: unsubstituted α‐terthiophene (Th3) and a thiophene‐derived macromonomer having an α‐terthiophene conjugated sequence and one Th3 bearing a PEG chain with molecular weight of 2000 as substitute at the 3‐position of the central heterocycle (Th3‐PEG2000). The grafting ratio of the resulting copolymers (PTh3*‐g‐PEG), which were obtained using 75:25 and 50:50 Th3‐PEG2000:Th3 weight ratios, is significantly smaller than that of copolymers derived from polymerization of macromonomers consisting of a α‐pentathiophene sequence in which the central ring bears a PEG chain of Mw = 2000 (PTh5‐g‐PEG). The electroactivity and electrochemical stability of PTh3*‐g‐PEG is not only higher than that of PTh5‐g‐PEG but also higher than that of PTh3, the latter presenting a very compact structure that makes difficult the access and escape of dopant ions into the polymeric matrix during the redox processes. Furthermore, the optical π‐π* lowest transition energy of PTh3*‐g‐PEG is lower than that of both PTh5‐g‐PEG and PTh3. These properties, combined with suitable wettability and roughness, result in an excellent behavior as bioactive platform of PTh3*‐g‐PEG copolymers, which are more biocompatible, in terms of cellular adhesion and proliferation, and electro‐compatible than PTh5‐g‐PEG. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 239–252 相似文献