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排序方式: 共有279条查询结果,搜索用时 15 毫秒
1.
Bekzat ABDIKADYR Alp KILI Onur ALEV Serkan BÜYÜKK
SE Zafer Ziya
ZTÜRK 《Turkish Journal of Chemistry》2021,45(2):295
Pristine and WO3 decorated TiO2 nanorods (NRs) were synthesised to investigate n-n-type heterojunction gas sensing properties. TiO2 NRs were fabricated via hydrothermal method on fluorine-doped tin oxide coated glass (FTO) substrates. Then, tungsten was sputtered on the TiO2 NRs and thermally oxidised to obtain WO3 nanoparticles. The heterostructure was characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) spectroscopy. Fabricated sensor devices were exposed to VOCs such as toluene, xylene, acetone and ethanol, and humidity at different operation temperatures. Experimental results demonstrated that the heterostructure has better sensor response toward ethanol at 200 °C. Enhanced sensing properties are attributed to the heterojunction formation by decorating TiO2 NRs with WO3. 相似文献
2.
Florian Venel Dr. Hiroki Nagashima Dr. Andrew G. M. Rankin Christelle Anquetil Dr. Vytautas Klimavicius Dr. Torsten Gutmann Prof. Gerd Buntkowsky Dr. Sylvie Derenne Prof. Olivier Lafon Dr. Arnaud Huguet Dr. Frédérique Pourpoint 《Chemphyschem》2021,22(18):1907-1913
Estuaries are key ecosystems with unique biodiversity and are of high economic importance. Along the estuaries, variations in environmental parameters, such as salinity and light penetration, can modify the characteristics of dissolved organic matter (DOM). Nevertheless, there is still limited information about the atomic-level transformations of DOM in this ecosystem. Solid-state NMR spectroscopy provides unique insights into the nature of functional groups in DOM. A major limitation of this technique is its lack of sensivity, which results in experimental time of tens of hours for the acquisition of 13C NMR spectra and generally precludes the observation of 15N nuclei for DOM. We show here how the sensitivity of solid-state NMR experiments on DOM of Seine estuary can be enhanced using dynamic nuclear polarization (DNP) under magic-angle spinning. This technique allows the acquisition of 13C NMR spectra of these samples in few minutes, instead of hours for conventional solid-state NMR. Both conventional and DNP-enhanced 13C NMR spectra indicate that the 13C local environments in DOM are not strongly modified along the Seine estuary. Furthermore, the sensitivity gain provided by the DNP allows the detection of 15N NMR signal of DOM, in spite of the low nitrogen content. These spectra reveal that the majority of nitrogen is in the amide form in these DOM samples and show an increased disorder around these amide groups near the mouth of the Seine. 相似文献
3.
Brent A. Rankin Joshua R. Codoni John L. Hoke Frederick R. Schauer 《Proceedings of the Combustion Institute》2019,37(3):3479-3486
The structure of detonation waves propagating through the annular channel of an optically accessible non-premixed rotating detonation engine (RDE) are investigated using mid-infrared imaging. The RDE is operated on hydrogen–air mixtures for a range of air mass flow rates and equivalence ratios. Instantaneous images of the radiation intensity from water vapor are acquired using a mid-infrared camera and a band-pass filter (2.890?±?0.033?µm). The instantaneous mid-infrared images reveal the stochastic nature of the detonation wave structure, position and angle of oblique and reflected shock waves, presence of shear layer separating products from the previous and current cycles, and extent of mixing between the reactants and products in the reactant fill zone in front of the detonation wave. The images show negligible signal directly in front of the detonation waves suggesting that there is minimal mixing between the reactants and products from the previous cycle ahead of the detonation wave for most operating conditions. The mid-infrared images provide insights useful for improving fundamental understanding of the detonation structure in RDEs and benchmark data for evaluating modeling and simulation results of RDEs. 相似文献
4.
Derek A. Wann Andrew R. Turner Jens R. Goerlich Lorna J. Kettle Reinhard Schmutzler David W. H. Rankin 《Structural chemistry》2011,22(2):263-267
The gas-phase structure of 1-adamantylphosphine has been determined by electron diffraction, supplemented with data from ab
initio and DFT calculations. The adamantyl fragment was modeled with local C
3v
symmetry and the phosphino group was found to be in a position almost bisecting a mirror plane of the adamantyl group, giving
the molecule overall approximate C
s
symmetry. There is a small displacement of the C–P bond from the local threefold axis of the adamantyl group. Geometry optimizations
were also performed for bis-(1-adamantyl)phosphine (C
1 point-group symmetry) and tris-(1-adamantyl)phosphine (C
3 symmetry), demonstrating extremely crowded environments around the phosphorus atoms leading to adamantyl groups that were
much less symmetric. The adamantyl groups were also found to twist by a significant amount to minimize the strain. 相似文献
5.
B. W. Bailey J. M. Rankin R. Weinbloom 《International journal of environmental analytical chemistry》2013,93(1):3-9
The use of ternary complexes in the determination of anionic surfactants has been investigated and an analytical method using linear alkyl sulfonates as a test substance has been developed. The method involves the formation of the chloroform-extractable bisphenanthroline Cu(II)-linear alkyl sulfonate (LAS) complex and the subsequent equilibration of the extract with erythrosine to form the extractable bisphenanthroline Cu(II)-erythrosine complex. In the equilibration step erythrosine displaces LAS quantitatively, allowing the determination of the LAS originally present by measuring the absorbance of the extracted bisphenanthroline-Cu(II)-erythrosine complex. Results are reported of studies made to determine the optimum analytical conditions, the sensitivity, and the precision for the method described. 相似文献
6.
Joanne E. Stanley Anthony C. Swain Kieran C. Molloy David W. H. Rankin Heather E. Robertson Blair F. Johnston 《应用有机金属化学》2005,19(5):644-657
Perfluoroalkytin compounds R(4−n)Sn(Rf)n (R = Me, Et, Bu, Rf = C4F9, n = 1; R = Bu, Rf = C4F9, n = 2, 3; R = Bu, Rf = C6F13, n = 1) have been synthesized, characterized by 1H, 13C, 19F and 119Sn NMR, and evaluated as precursors for the atmospheric pressure chemical vapour deposition of fluorine‐doped SnO2 thin films. All precursors were sufficiently volatile in the range 84–136 °C and glass substrate temperatures of ca 550 °C to yield high‐quality films with ca 0.79–2.02% fluorine incorporation, save for Bu3SnC6F13, which incorporated <0.05% fluorine. Films were characterized by X‐ray diffraction, scanning electron microscopy, thickness, haze, emissivity, and sheet resistance. The fastest growth rates and highest quality films were obtained from Et3SnC4F9. An electron diffraction study of Me3SnC4F9 revealed four conformations, of which only the two of lowest abundance showed close F Sn contacts that could plausibly be associated with halogen transfer to tin, and in each case it was fluorine attached to either the γ‐ or δ‐carbon atoms of the Rf chain. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
7.
The electrophilic addition reactions of methylsulfenyl chloride to the double bonds of functionalized ethenes have been studied theoretically. Density functional theory (DFT) calculations have been applied for starting species and ethene‐based sulfonium intermediates bearing substitutes at α‐carbon atom to study geometrical parameters and electronic states of plausible intermediate forms. The quantum chemical optimizations of intermediates indicate that the episulfonium ion is the most likely methyl‐ or carboxyl‐substituted ethane‐based intermediate. However, with phenyl substituents the intermediate is more like a carbonium than an episulfonium ion. The role of sulfur appears to be that of directing the stereochemistry of the addition reaction of chloride, forming the trans product upon nucleophilic attack on the C—C bond of the episulfonium ion. The regioselectivity features of the opening of the episulfonium ion by the chloride anion depend on the LUMO and LUMO+1 of the episulfonium ion and the approaching HOMO of chlorine. The results of the theoretical investigations are in agreement with experiment. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:695–703, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20378 相似文献
8.
9.
Wm. Lerch R. H. Bogue E. S. Shepherd G. A. Rankin F. E. Wright F. Ferrari J. Stanton Pierce W. C. Setzer F. Strumpf und R. H. H. Stanger 《Fresenius' Journal of Analytical Chemistry》1930,81(12):476-480
Ohne Zusammenfassung 相似文献
10.
F. J. Reithel A. Farkas L. Farkas C. W. Sullens W. Rankin A. L. Olsen S. Kiyomizu G. F. Liebig Jr J. S. Mc Hargue E. B. Offutt P. R. Stout D. I. Arnon A. J. Bailey und S. Liotta 《Fresenius' Journal of Analytical Chemistry》1942,124(7-8):300-305
Ohne Zusammenfassung 相似文献