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121.
Ionics - Poly(vinylidene fluoride) (PVDF)/sodium hydrogen carbonate (NaHCO3)-based microporous polymer membranes were prepared by salt leaching. In this study, lithium-trifluoromethane sulfonate...  相似文献   
122.
This paper presents an ultra low-voltage, ultra low-power, very compact, dynamic threshold voltage MOS transistor (DTMOS)-based CCII circuit. The proposed circuit is capable of operating under ± 0.2 V symmetric supply voltages. The circuit topology is very compact and consists of only four DTMOS transistors and four ordinary NMOS transistors. The total power consumption of the circuit is found as only 214 nW while all transistors are working in the subthreshold region. The current conveyor has 570 kHz 3 dB-bandwidth from X to Y terminal for the voltage gain and has low, 0.2 % following error between these terminals for inputs not exceeding ± 60 mV. TSMC 0.18 µm process technology parameters are used in the design of the proposed CCII block which is then employed in an audio-frequency, second-order, band-pass filter configuration where real speech signals are fed to the input of the filter to further investigate its characteristics. Close agreement is found between theoretical study and simulated responses.  相似文献   
123.
In this study, the radical cyclization reactions of cyclic 1,3-dicarbonyl compounds (1a–c) and α,β-unsaturated alcohols (2a–d) through Mn(OAc)3 were performed. A series of biologically interesting dihydropyrans (3–5) and dihydrofurans (6–18) were synthesized as a result of these reactions. Spiro compounds (19–20) were obtained from the reactions of 1,3-dicarbonyl compounds and (E)-2,4-diphenyl-but-3-en-2-ol (2e). The unique structure of compound 19 was also confirmed by X-ray crystallography. In addition, the antibacterial activities of synthesized compounds were screened against some bacteria. Their zone diameters showed better results than some known antibiotics.  相似文献   
124.
Spatial and temporal control over chemical and biological processes, both in terms of “tuning” products and providing site‐specific control, is one of the most exciting and rapidly developing areas of modern science. For synthetic chemists, the challenge is to discover and develop selective and efficient reactions capable of generating useful molecules in a variety of matrices. In recent studies, light has been recognized as a valuable method for determining where, when, and to what extent a process is started or stopped. Accordingly, this Minireview will present the fundamental aspects of light‐induced click reactions, highlight the applications of these reactions to diverse fields of study, and discuss the potential for this methodology to be applied to the study of biomolecular systems.  相似文献   
125.
This paper describes the use of IBC??s AnaLig®Sr-01 molecular recognition technology product to effectively and selectively pre-concentrate, separate and recover strontium from radioactive waste samples. The use and effectiveness of AnaLig®Sr-01 gel was successfully validated by analysis of International Atomic Energy Agency (IAEA 375) reference soil and National Physical Laboratory (NPL)?CHigh Alpha?CBeta (2003) liquid sample. The second part of this paper focuses on analysis of radioactive waste samples from nuclear power plant A1 Jaslovske Bohunice in Slovak Republic (NPP A1).  相似文献   
126.
UV‐curable fluorinated organic–inorganic hybrid coatings were prepared by the sol–gel technique. Perfluorinated urethane modified alkoxysilane was synthesized by the reaction between perfluoro alcohol and 3‐isocyanatopropyltrimethoxysilane. The prepared formulations were applied onto poly(methyl methacrylate) (PMMA) and acrylonitrile butadiene styrene (ABS) panels and polymerized by UV‐curing. The properties of the hybrid coatings such as hardness, chemical resistance, thermal stability, surface morphology, double bond conversion, and also contact angle measurements were investigated. Contact angle measurements have shown that the addition of fluorinated silane precursor to the hybrid system improved the water repellency and increased the contact angle from 65° to 106°. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   
127.
This study describes the use of diphenyliodonium salts with highly nucleophilic counter anions to photoinitiate the cationic cross‐linking of divinyl ethers. Both direct and indirect initiating modes are used. In the direct acting system, only a diphenyliodonium salt with a highly nucleophilic counter anion and a zinc halide are employed as initiator and activator, respectively. In the indirect systems, in addition to direct system components, photosensitive additives such as anthrecene, perylene, 2,2‐dimethoxy‐2‐phenyl acetophenone, benzophenone, and thioxanthone, which absorb the energy of the incident light and activate the iodonium salt, are used to initiate polymerization. All systems employed in this study initiated quite vigorous polymerizations.

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