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排序方式: 共有260条查询结果,搜索用时 15 毫秒
21.
Dr. Krystle C. H. Chua Dr. Markus Pietsch Xiaozhou Zhang Stephanie Hautmann Hon Y. Chan Dr. John B. Bruning Prof. Dr. Michael Gütschow Prof. Dr. Andrew D. Abell 《Angewandte Chemie (International ed. in English)》2014,53(30):7828-7831
There is a real need for simple structures that define a β‐strand conformation, a secondary structure that is central to peptide–protein interactions. For example, protease substrates and inhibitors almost universally adopt this geometry on active site binding. A planar pyrrole is used to replace two amino acids of a peptide backbone to generate a simple macrocycle that retains the required geometry for active site binding. The resulting β‐strand templates have reduced peptide character and provide potent protease inhibitors with the attachment of an appropriate amino aldehyde to the C‐terminus. Picomolar inhibitors of cathepsin L and S are reported and the mode of binding of one example to the model protease chymotrypsin is defined by X‐ray crystallography. 相似文献
22.
Liang Zhang Jinghua Teng Soo Jin Chua Eugene A. Fitzgerald 《Applied Physics A: Materials Science & Processing》2011,103(3):827-830
Linearly polarized light from InGaN green light emitting diode grown on (0001) oriented sapphire is demonstrated by using
subwavelength metallic nanogratings. Polarization ratio can reach 7:1 (∼88%), the highest ever reported from a single light
emitting device. We discuss the design and fabrication of this device in detail. 相似文献
23.
Two recent experimental developments, when combined, may have far-reaching implications. S(phiK(S))<0, if confirmed, would imply large s-b mixing, a new CP phase, and right-handed dynamics. Large Deltam(B(s)) would be likely, making the B(s) program at hadron machines difficult. Reconstruction of B vertex from K(S) at B factories, as shown by BaBar's first measurement of SK(S)(pi(0)), makes SK(S)(pi(0)gamma) in B-->K(*0)gamma accessible. This would be a boon for B factory upgrades. Supersymmetric Abelian flavor symmetry, independently motivated, can realize all of this with a light sb(1) squark. B factory and collider studies of flavor, CP and supersymmetry, may not be what we had expected. 相似文献
24.
Lin Ke Shuang Fang Lim Soo Jin Chua 《Journal of Polymer Science.Polymer Physics》2001,39(14):1697-1703
Dark spot growth rate tracing experiments performed on an organic light‐emitting device show that moisture entering into the device is relatively properly fitted by Fick's diffusion equation in the substrate/indium tin oxide (ITO)/hole transport layer (HTL)/silver (Ag) structure. It is believed that the moisture is dissolved into the polymer layer, which results in a decrease in the diffusion coefficient in the device with the substrate/ITO/HTL/electroluminescent (EL) polymer/Ag structure. The diffusion and chemical reaction occurring in the cathode layer further decreases the diffusion coefficient in the device with the substrate/ITO/HTL/EL polymer/calcium/Ag structure. Useful parameters, such as diffusion and solubility constants, describing possible mechanisms happening during dark spot growth on organic light‐emitting diode devices are extracted. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1697–1703, 2001 相似文献
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This study investigates the cellulose–lignin interactions during fast pyrolysis at 100–350 °C for better understanding fundamental pyrolysis mechanism of lignocellulosic biomass. The results show that co-pyrolysis of cellulose and lignin (with a mass ratio of 1:1) at temperatures < 300 °C leads to a char yield lower than the calculated char yield based on the addition of individual cellulose and lignin pyrolysis. The difference between the experimental and calculated char yields increases with temperature, from ~2% 150 °C to ~6% at 250 °C. Such differences in char yields provide direct evidences on the existence of cellulose–lignin interactions during co-pyrolysis of cellulose and lignin. At temperatures below 300 °C, the reductions in both lignin functional groups and sugar structures within the char indicate that co-pyrolysis of cellulose and lignin enhances the release of volatiles from both cellulose and lignin. Such an observation could be attributed to two possible reasons: (1) the stabilization of lignin-derived reactive species by cellulose-derived reaction intermediates as hydrogen donors, and (2) the thermal ejection of cellulose-derived species due to micro-explosion of liquid intermediates from lignin. In contrast, at temperatures ≥ 300 °C, co-pyrolysis of cellulose and lignin increases char yields, i.e., with the difference between the experimental and calculated char yields increasing from ~1% at 300 °C to ~8% at 350 °C. The results indicate that the cellulose-derived volatiles are difficult to diffuse through the lignin-derived liquid intermediates into the vapor phase, leading to increased char formation from co-pyrolysis of cellulose and lignin as temperature increases. Such an observation is further supported by the increased retention of cellulose functional groups in the char from co-pyrolysis of cellulose and lignin. 相似文献
28.
We compare two methods of calibrating the yaw response of hot-wire probes: (i) the assumption that an effective angle, independent
of the flow speed, can be deduced; (ii) the more general approach of determining the yaw response at a number of different
speeds. The first, simpler, approach is shown to give surprisingly reasonable results for the usual turbulence statistics,
even in high turbulence intensity flows. Some differences in the distribution of the inclination of the instantaneous velocity
vector are observed. There is no advantage in using thek
2 factor to allow for longitudinal cooling. 相似文献
29.
Misfit‐Layered Bi1.85Sr2Co1.85O7.7−δ for the Hydrogen Evolution Reaction: Beyond van der Waals Heterostructures 下载免费PDF全文
Dr. Chun Kiang Chua Prof. Zdeněk Sofer Ondřej Jankovský Prof. Martin Pumera 《Chemphyschem》2015,16(4):769-774
Recent research on stable 2D nanomaterials has led to the discovery of new materials for energy‐conversion and energy‐storage applications. A class of layered heterostructures known as misfit‐layered chalcogenides consists of well‐defined atomic layers and has previously been applied as thermoelectric materials for use as high‐temperature thermoelectric batteries. The performance of such misfit‐layered chalcogenides in electrochemical applications, specifically the hydrogen evolution reaction, is currently unexplored. Herein, a misfit‐layered chalcogenide consisting of CoO2 layers interleaved with an SrO–BiO–BiO–SrO rock‐salt block and having the formula Bi1.85Sr2Co1.85O7.7?δ is synthesized and examined for its structural and electrochemical properties. The hydrogen‐evolution performance of misfit‐layered Bi1.85Sr2Co1.85O7.7?δ, which has an overpotential of 589 mV and a Tafel slope of 51 mV per decade, demonstrates the promising potential of misfit‐layered chalcogenides as electrocatalysts instead of classical carbon. 相似文献
30.
The environmental remediation of military installation sites is very important due to frequently large presence of carcinogenic derivatives of explosives in the ground and in ground waters. These nitroaromatic explosives and their derivatives are assessed by sensing devices. It is highly important to have insight on the reasons affecting the reduction potentials of these compounds. The redox properties of mono‐, di‐ and tri‐nitroaromatic compounds are studied with cyclic voltammetry at a glassy carbon electrode for comparison. We show that the presence of a methyl group in the aromatic system leads into more negative reduction potentials. The ease of nitro group reduction vary from meta>para>ortho positions relative to a methyl group. The redox properties were also studied at various pH ranging from 2 to 10. Acidic environments facilitated the reduction processes at lower potentials. These findings will have a profound influence upon understanding the processes during reductive decontaminations of the polluted sites as well as for construction of highly sensitive sensors for their determination. 相似文献