全文获取类型
收费全文 | 374篇 |
免费 | 4篇 |
国内免费 | 2篇 |
专业分类
化学 | 208篇 |
晶体学 | 1篇 |
力学 | 8篇 |
数学 | 90篇 |
物理学 | 73篇 |
出版年
2023年 | 3篇 |
2022年 | 8篇 |
2021年 | 18篇 |
2020年 | 8篇 |
2019年 | 11篇 |
2018年 | 12篇 |
2017年 | 7篇 |
2016年 | 17篇 |
2015年 | 4篇 |
2014年 | 13篇 |
2013年 | 21篇 |
2012年 | 24篇 |
2011年 | 26篇 |
2010年 | 19篇 |
2009年 | 17篇 |
2008年 | 19篇 |
2007年 | 16篇 |
2006年 | 16篇 |
2005年 | 16篇 |
2004年 | 9篇 |
2003年 | 11篇 |
2002年 | 8篇 |
2001年 | 7篇 |
2000年 | 5篇 |
1999年 | 2篇 |
1998年 | 3篇 |
1996年 | 2篇 |
1995年 | 3篇 |
1994年 | 4篇 |
1993年 | 2篇 |
1992年 | 2篇 |
1990年 | 2篇 |
1987年 | 2篇 |
1986年 | 2篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1982年 | 2篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1978年 | 2篇 |
1977年 | 1篇 |
1976年 | 2篇 |
1975年 | 2篇 |
1974年 | 4篇 |
1973年 | 7篇 |
1972年 | 2篇 |
1970年 | 1篇 |
1969年 | 4篇 |
1967年 | 1篇 |
1903年 | 1篇 |
排序方式: 共有380条查询结果,搜索用时 15 毫秒
21.
Chekmarev DS Lazareva MI Zatonsky GV Maskaev AV Caple R Smit W 《The Journal of organic chemistry》2002,67(23):7957-7967
Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products containing either cyclohexane or 1,3-diene units are described. 相似文献
22.
Prof. Vladimir K. Cherkasov Prof. Gleb A. Abakumov Dr. Georgy K. Fukin Dr. Svetlana V. Klementyeva Dr. Viacheslav A. Kuropatov 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(43):13821-13827
A new stable sterically hindered o‐quinone annelated with a 1,2‐dithiete ring was prepared by using mild conditions. The skeleton of the compound comprises diolate and dithiolate functions that have the potential to bind metals leading to the corresponding complexes. The reactivity of this compound as a ligand with respect to both coordination sites was studied. Reactions with metals indicate that the o‐quinone function is reduced in the first stage to give semiquinonate and catecholate complexes. The dithiolate coordination site was involved in the reaction in a few cases only after diolate was bound. A trinuclear manganese complex with coordination on both sites was obtained and characterized by EPR spectroscopy. The electrochemical study of this quinone fused with dithiete is reported. 相似文献
23.
Georgy M. Pavlov Anke Teichler Stephanie Höppener Christine Weber Jürgen Nowotny Lars Blankenburg Jürgen Popp Martin D. Hager Benjamin Dietzek Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2012,50(15):3192-3205
In order to form suitable systems designed for resonance energy transfer, a series of monodisperse methacrylate‐based monomers containing rigid π‐conjugated oligo(phenylene ethynylenes) with different sizes of the conjugated systems ( M1 – M3 ), and therefore different optoelectronic properties, were synthesized and subsequently polymerized using the reversible addition–fragmentation chain transfer polymerization technique ( P1 – P3 ). In addition, these oligomers were also copolymerized with methyl methacrylate. The obtained polymers were characterized by 1H NMR spectroscopy, size exclusion chromatography, and analytical ultracentrifugation. The photophysical properties of the polymers were studied by UV–vis absorption and emission spectroscopy in diluted solutions as well as in thin films and compared to the photophysics of the corresponding monomers. Thereby, changes going from monomeric to polymeric systems could be detected in fluorescence quantum yields and lifetimes pointing to energy trapping, e.g., energy transfer. Donor–acceptor copolymers containing different numbers of monomeric units within the side chain exhibit differences in the emission spectra, indicating that energy trapping in polymers is very sensitive to structural properties such as the chain length. UV–vis absorption spectroscopy as well as time‐resolved lifetime studies indicate intrapolymer and interpolymer energy transfer. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
24.
Valentine G Nenajdenko Georgy N Varseev Alexey V Shastin 《Journal of fluorine chemistry》2003,124(1):115-118
A novel catalytic approach to (2,2-difluorovinyl)benzenes has been developed. It was found that hydrazones of aromatic aldehydes generated in situ could be converted to the corresponding (2,2-difluorovinyl)benzenes by catalytic olefination reaction (COR) with dibromodifluoromethane in the presence of CuCl. 相似文献
25.
26.
Trifonov AA Fedorova EA Fukin GK Baranov EV Druzhkov NO Bochkarev MN 《Chemistry (Weinheim an der Bergstrasse, Germany)》2006,12(10):2752-2757
The redox reaction of [Yb(C(9)H(7))(2)(thf)(2)] with the diazabutadiene PhN==C(Me)--C(Me)==NPh (DAD) has been found to depend on the molar ratio of the reactants. Reaction in a 1:2 molar ratio affords the dinuclear mixed-valent complex [Yb(2)(mu-eta(5):eta(4)-C(9)H(7))(eta(5)-C(9)H(7))(2){mu-eta(4):eta(4)-PhNC(Me)==C(Me)NPh}] containing an indenyl ligand with an unusual mu-eta(5):eta(4) bridging coordination. Reaction of equimolar amounts of these compounds results in an organolanthanide-mediated reductive coupling of the DAD ligands and formation of the tetranuclear mixed-valent complex [Yb(2)(mu-eta(5):eta(4)-C(9)H(7))(eta(5)-C(9)H(7))(2){mu-eta(4):eta(4)-PhNC(CH(2))==C(Me)NPh}](2) with a novel tetradentate tetraimine ligand. 相似文献
27.
Willans CE Sinenkov MA Fukin GK Sheridan K Lynam JM Trifonov AA Kerton FM 《Dalton transactions (Cambridge, England : 2003)》2008,(27):3592-3598
Reaction of two equivalents of n-BuLi with sterically demanding amine-bis(phenol) compounds, H(2)O(2)NN'(R) (Me(2)NCH(2)CH(2)N{CH(2)-3,5-R(2)-C(6)H(2)OH}(2); R = t-Bu or t-Pe (tert-pentyl)) yields isolable lithium complexes, Li(2)(O(2)NN'(R)), in good yields. Upon reaction with one equivalent of LnCl(3)(THF)(x), the lithium salts afford rare earth amine-phenolate chloride complexes in good yields, Ln(O(2)NN'(R))Cl(THF); Ln = Y, Yb, Ho, Gd, Sm, Pr. Crystals of Y(O(2)NN'(t-Bu))Cl(THF), 1, and Sm(O(2)NN'(t-Bu))Cl(DME), 2, suitable for single crystal X-ray crystallographic analysis were obtained. In contrast to previously reported [{Gd(O(2)NN'(t-Pe))(THF)(micro-Cl)}(2)] and related La and Sm complexes, these species are monomeric. 1 contains Y in a distorted octahedral environment bonded to two amine, two phenolate, one THF and one chloride donor. 2 contains Sm in a distorted capped trigonal prismatic environment bonded to two amine, two phenolate, two DME oxygens and one chloride donor. The Ln(O(2)NN'(t-Pe))Cl(THF) complexes were active initators for the controlled ring-opening polymerization of epsilon-caprolactone with a tendency to form low molecular weight cyclic polyesters (M(n) 3000-5000). The conversion rates, although slower than related amido and alkyl species, were different for monomeric and dimeric initiators. The size of the metal centre also affected the conversions and the molecular weights achieved. 相似文献
28.
G. A. Kostin A. O. Borodin Yu. V. Shubin N. V. Kurat’eva V. A. Emelyanov P. E. Plyusnin M. R. Gallyamov 《Russian Journal of Coordination Chemistry》2009,35(1):57-64
Three new heteronuclear complexes [Ru(NO)(NO2)4(OH)M(Py)3] (M = Co2+, Ni2+, Zn2+) were synthesized and structurally characterized. In all compounds, the [Ru(NO)(NO2)4(OH)] fragment is coordinated to the M atom by a bridging OH and two bridging NO2 groups. The coordination environment of the metal also includes three pyridine nitrogen atoms. Thermal decomposition of cobalt
and nickel complexes in an inert atmosphere yields bimetallic solid solutions.
Original Russian Text ? G.A. Kostin, A.O. Borodin, Yu.V. Shubin, N.V. Kurat’eva, V.A. Emelyanov, P.E. Plyusnin, M.R. Gallyamov,
2009, published in Koordinatsionnaya Khimiya, 2009, Vol. 35, No. 1, pp. 57–64. 相似文献
29.
The superelectrophilic activation of N-aryl amides of 3-arylpropynoic acids by Bronsted superacids (CF3SO3H, HSO3F) or strong Lewis acids AlX3 (X=Cl, Br) results in the formation of 4-aryl quinolin-2(1H)-ones in quantitative yields. The vinyl triflates or vinyl chlorides may be formed as additional reaction products. The investigated amides in reactions with benzene give 4,4-diaryl 3,4-dihydroquinolin-2-(1H)-ones under the superelectrophilic activation. 4-Aryl quinolin-2(1H)-ones in POCl3 are converted into 4-aryl 2-chloroquinolines. 4-Fluorophenyl-4-phenyl 3,4-dihydroquinolin-2-(1H)-one give N-formylation products in a yield of 79% under the Vilsmeier–Haack reaction conditions. 相似文献
30.