全文获取类型
收费全文 | 589篇 |
免费 | 31篇 |
专业分类
化学 | 505篇 |
晶体学 | 1篇 |
力学 | 4篇 |
数学 | 38篇 |
物理学 | 72篇 |
出版年
2024年 | 2篇 |
2023年 | 7篇 |
2022年 | 9篇 |
2021年 | 11篇 |
2020年 | 10篇 |
2019年 | 15篇 |
2018年 | 9篇 |
2017年 | 3篇 |
2016年 | 21篇 |
2015年 | 19篇 |
2014年 | 25篇 |
2013年 | 28篇 |
2012年 | 43篇 |
2011年 | 50篇 |
2010年 | 42篇 |
2009年 | 26篇 |
2008年 | 49篇 |
2007年 | 41篇 |
2006年 | 29篇 |
2005年 | 38篇 |
2004年 | 31篇 |
2003年 | 28篇 |
2002年 | 12篇 |
2001年 | 3篇 |
2000年 | 5篇 |
1999年 | 7篇 |
1998年 | 4篇 |
1997年 | 5篇 |
1996年 | 5篇 |
1995年 | 3篇 |
1993年 | 2篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1989年 | 2篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 4篇 |
1984年 | 3篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1980年 | 4篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1970年 | 1篇 |
1969年 | 1篇 |
排序方式: 共有620条查询结果,搜索用时 0 毫秒
71.
Martin Gericke Katja Geitel Cornelia Jrke Joachim H. Clement Thomas Heinze 《Molecules (Basel, Switzerland)》2021,26(13)
Polysaccharide (PS) based nanoparticles (NP) are of great interest for biomedical applications. A key challenge in this regard is the functionalization of these nanomaterials. The aim of the present work was the development of reactive PS-NP that can be coupled with an amino group containing compounds under mild aqueous conditions. A series of cellulose phenyl carbonates (CPC) and xylan phenyl carbonates (XPC) with variable degrees of substitution (DS) was obtained by homogeneous synthesis. The preparation of PS-NP by self-assembling of these hydrophobic derivatives was studied comprehensively. While CPC mostly formed macroscopic aggregates, XPC formed well-defined spherical NP with diameters around 100 to 200 nm that showed a pronounced long-term stability in water against both particle aggregation as well as cleavage of phenyl carbonate moieties. Using an amino group functionalized dye it was demonstrated that the novel XPC-NP are reactive towards amines. A simple coupling procedure was established that enables direct functionalization of the reactive NP in an aqueous dispersion. Finally, it was demonstrated that dye functionalized XPC-NP are non-cytotoxic and can be employed in advanced biomedical applications. 相似文献
72.
Katja Jankova Melania Bednarek Sren Hvilsted 《Journal of polymer science. Part A, Polymer chemistry》2005,43(17):3748-3759
Multifunctional initiators for atom transfer radical polymerization (ATRP) are prepared by converting ditrimethylolpropane with four hydroxyl groups, dipentaerythritol with six hydroxyl groups, and poly(3‐ethyl‐3‐hydroxymethyl‐oxetane) with ~11 hydroxyl groups to the corresponding 2‐bromoisobutyrates or 2‐bromopropionates as obtained by reaction with acid bromides. Star polystyrene (PS) is produced by using these macroinitiators and neat styrene in a controlled manner by ATRP at 110 °C, employing the catalytic system CuBr and bipyridine. Mn up to 51,000 associated with narrow molecular weight distributions (PDI < 1.1) are obtained with conversions up to 32%. Hydrolysis of the star‐PS leads to linear chains having the expected Mn values. The star‐PS polymers based on dipentaerythritol degrade thermally in nitrogen in a two‐step process in which the first low‐temperature step involves scission of the ester linkages and the second step corresponds to the normal PS degradation. Star poly(methyl acrylates) with various cores are likewise prepared in a controlled manner by ATRP of methyl acrylate in bulk and in solution at 60–80 °C with the 1,1,4,7,7‐pentamethyldiethylene triamine ligand. Under these conditions, higher conversions were possible still maintaining low PDI signaling controlled star growth. Multiarm stars of poly(n‐butyl acrylate) and poly(n‐hexyl acrylate) with controlled characteristics have also been prepared. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3748–3759, 2005 相似文献
73.
Franz‐Josef K. Rehmann Laurence P. Cuffe Oscar Mendoza Dilip K. Rai Nigel Sweeney Katja Strohfeldt William M. Gallagher Matthias Tacke 《应用有机金属化学》2005,19(3):293-300
Starting from 2‐furylfulvene (1a) , 2‐thiophenylfulvene (1b) , and 1‐methyl‐2‐pyrrolylfulvene (1c), [1,2‐di(cyclopentadienyl)‐1,2‐di‐(2‐furyl)ethanediyl] titanium dichloride (2a) , [1,2‐di(cyclopentadienyl)‐1,2‐di‐(2‐thiophenyl)ethanediyl] titanium dichloride (2b) , and [1,2‐di(cyclopentadienyl)‐1,2‐bis‐(1‐methyl‐2‐pyrrolyl)ethanediyl] titanium dichloride (2c) were synthesized. When titanocenes (2a–c) were tested against pig kidney carcinoma cells (LLC‐PK), inhibitory concentrations (50%) of 4.5 × 10?4 M , 2.9 × 10?4 M and 2.0 × 10?4 M respectively were observed. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
74.
Smrati Gupta Dirk Kuckling Katja Kretschmer Veena Choudhary Hans‐Jürgen Adler 《Journal of polymer science. Part A, Polymer chemistry》2007,45(4):669-679
The aim of this work was the development of a versatile route for the preparation of temperature‐ and pH‐responsive hydrogels with small dimensions. The copolymerization of N,N‐dimethylaminoethyl methacrylate with various amounts (5 and 10 mol %) of dimethylmaleimidoethyl methacrylate in solution with 2,2′‐azobisisobutyronitrile as an initiator is described. The structural and molecular characterization of the copolymers was performed with proton nuclear magnetic resonance, Fourier transform infrared, and ultraviolet spectroscopy, as well as size exclusion chromatography. Differential scanning calorimetry and thermogravimetry were used for the thermal characterization of the copolymers. Micro‐ and nanohydrogels of the copolymers were prepared by photocrosslinking. The gels obtained by photocrosslinking were characterized with a combination of surface plasmon resonance and optical waveguide spectroscopy, dynamic light scattering, and scanning electron microscopy. The hydrogels showed temperature‐ and pH‐responsive behavior. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 669–679, 2007 相似文献
75.
76.
Gerrit Gobius du Sart Ivana Vukovic Zorica Vukovic Evgeny Polushkin Panu Hiekkataipale Janne Ruokolainen Katja Loos Gerrit ten Brinke 《Macromolecular rapid communications》2011,32(4):366-370
Supramolecular complexes of a poly(tert‐butoxystyrene)‐block‐polystyrene‐block‐poly(4‐vinylpyridine) triblock copolymers and less than stoichiometric amounts of pentadecylphenol (PDP) are shown to self‐assemble into a core–shell gyroid morphology with the core channels formed by the hydrogen‐bonded P4VP(PDP)complexes. After structure formation, PDP was removed using a simple washing procedure, resulting in well‐ordered nanoporous films that were used as templates for nickel plating.
77.
2H/1H isotope ratios of polyhalogenated compounds were determined by elemental analysis and isotope ratio mass spectrometry (EA-IRMS).
Initial measurements with standard EA-IRMS equipment, which used high-temperature pyrolysis to convert the organic compounds
into hydrogen, did not achieve significant signals for polychlorinated pesticides and related compounds, presumably due to
the formation of HCl instead of hydrogen. To reverse this problematic reaction, a chromium reactor was incorporated into the
element analyzer system, which scavenged Cl, forming chromium chloride and releasing hydrogen again in the form of H2. The optimized system therefore allowed the δ2H values of polyhalogenated compounds to be determined. A quality assurance program was developed based on several parameters.
(i) Each compound was analyzed using a sequence of five injections, where the first measurement was discarded. (ii) Recovery
of H (when calculated relative to acetanilide) had to be >90% for all replicates in a sequence. (iii) All δ-values within
a sequence had to vary by less than 10‰. (iv) Results had to be reproducible on another day with a different sample scheme.
Once this reproducibility had been established, variabilities in the δ2H values of organohalogen standards were investigated using the technique. The highest δ2H value of +75‰ was found for o,p′-DDD, whereas the strongest depletion in deuterium was found for Melipax (–181‰). The most important results for comparable
compounds were as follows. DDT-related compounds gave δ2H values of between +59 and +75‰ (technical DDT, o,p′- and p,p′-DDD) or in the range of approximately −1‰, indicative of the different sources/methods of producing this compound. Four
HCH isomers from the same supplier showed relatively similar hydrogen isotope distributions, whereas two lindane (γ–HCH) standards
from other sources had 39‰ less deuterium. This difference is likely due to different purification steps during the isolation
of pure lindane from the technical HCH mixture. An even greater difference was observed between the δ2H values of Toxaphene (US product dating from 1978) and Melipax (product from the former East Germany, dating from 1979),
which gave δ2H values of –101‰ and –181‰, respectively, meaning that both products were easily distinguished via δ2H-IRMS. Fractioning of hydrogen isotopes in the atmospheric water cycle was suggested as one reason for the different values.
In this theory, the water (which had different δ2H values depending on where it was taken from) was incorporated during the biosynthesis of camphene, which is the natural
product used to produce both products. These results indicate that hydrogen isotope-specific analysis can be a valuable tool
for tracing the origins of a compound in certain cases. 相似文献
78.
We study the efficiency at maximum power, η*, of engines performing finite-time Carnot cycles between a hot and a cold reservoir at temperatures Th and Tc, respectively. For engines reaching Carnot efficiency ηC=1-Tc/Th in the reversible limit (long cycle time, zero dissipation), we find in the limit of low dissipation that η* is bounded from above by ηC/(2-ηC) and from below by ηC/2. These bounds are reached when the ratio of the dissipation during the cold and hot isothermal phases tend, respectively, to zero or infinity. For symmetric dissipation (ratio one) the Curzon-Ahlborn efficiency ηCA=1-√Tc/Th] is recovered. 相似文献
79.
We present the simplest discrete model to date that leads to synchronization of stochastic phase-coupled oscillators. In the mean field limit, the model exhibits a Hopf bifurcation and global oscillatory behavior as coupling crosses a critical value. When coupling between units is strictly local, the model undergoes a continuous phase transition which we characterize numerically using finite-size scaling analysis. In particular, the onset of global synchrony is marked by signatures of the XY universality class, including the appropriate classical exponents beta and nu, a lower critical dimension d(lc) = 2, and an upper critical dimension d(uc) = 4. 相似文献
80.
Fan (in Southeast Asian Bull Math 25, 217–221, 2001) determines the endomorphism type of a finite projective plane. In this note we show that Fan’s result actually characterizes the class of projective planes among the finite bipartite graphs of diameter three. In fact, this will follow from a generalization of Fan’s theorem and its converse to all finite bipartite graphs with diameter d and girth g such that (1) d + 1<g≤2d, and (2) every pair of adjacent edges is contained in a circuit of length g. 相似文献