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31.
R.O. Dillon I.L. Spain J.A. Woollam W.H. Lowrey 《Journal of Physics and Chemistry of Solids》1978,39(9):907-922
Measurements of the galvanomagnetic properties of highly-oriented pyrolytic graphite have been made in the field range 0.001–1.5 T at 298, 77.4 and 4.2 K, with selected measurements to higher fields and ~1.2K. Specimens of graphite were chosen with properties approximating those of purified natural crystals (single crystals) of graphite. Attention is drawn to differences in the properties of these materials. The data are analyzed with particular emphasis on the density of free carriers and its dependence on temperature, since earlier work had shown that experimental results were appreciably different from theoretical predictions. 相似文献
32.
Anomalies in the resonance dispersion of the pressure-broadened water vapor line at υ0 = 22.235 GHz, which were reported in Part I,(1) are resolved. The pressure-scanning differential-refraction spectrometer (microwave dispersometer) gives rise to a signal enhancement as the line center moves within the width of the dispersion discriminator which is a dual-mode transmission cavity. Resonance absorption prevents the frequency of peak transmitted power from coinciding with the resonance condition of zero phase, thus systematically distorting the molecular resonance dispersion. An expression, valid for |υ − υ0| greater than the cavity half width, is derived which predicts apparent departure from Lorentzian behavior. The results reported in I as well as results for the 23.6 GHz rotational 31,2 → 32,1 line of C2H4O (ethylene oxide) show a Lorentzian molecular line shape. At pressures above 1 torr nonresonant polarization effects become detectable. Instrumental distortion, and Doppler-, wall-, and saturation-broadening effects at low pressures (<50 mtorr) are accounted for only qualitatively to determine the resolving power and to define v0. 相似文献
33.
The technique of pulsed laser photolysis was coupled to laser induced fluorescence detection of iodine oxide (IO) to measure rate coefficients, k for the reactions IO + CH(3)O(2)--> products (R1, 30-318 Torr N(2)), IO + CF(3)O(2)--> products (R2, 70-80 Torr N(2)), and IO + O(3)--> OIO + O(2) (R3a). Values of k(1) = (2 +/- 1) x 10(-12) cm(3) molecule(-1) s(-1), k(2) = (3.6 +/- 0.8) x 10(-11) cm(3) molecule(-1) s(-1), and k(3a) <5 x 10(-16) cm(3) molecule(-1) s(-1) were obtained at T = 298 K. In the course of this work, the product yield of IO from the reaction of CH(3)O(2) with I was determined to be close to zero, whereas CH(3)OOI was formed efficiently at 70 Torr N(2). Similarly, no evidence was found for IO formation in the CF(3)O(2) + I reaction. An estimate of the rate coefficients k(CH(3)O(2) + I) = 2 x 10(-11) cm(3) molecule(-1) s(-1) and k(CH(3)OOI + I) = 1.5 x 10(-10) cm(3) molecule(-1) s(-1) was also obtained. The results on k(1)-k(3) are compared to the limited number of previous investigations and the implications for the chemistry of the marine boundary layer are briefly discussed. 相似文献
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35.
The occlusion effect is commonly described as an unnatural and mostly annoying quality of the voice of a person wearing hearing aids or hearing protectors. As a result, it is often reported by hearing aid users as a deterrent to wearing hearing aids. This paper presents an investigation into active occlusion cancellation. Measured transducer responses combined with models of an active feedback scheme are first examined in order to predict the effectiveness of occlusion reduction. The simulations predict 18 dB of occlusion reduction in completely blocked ear canals. Simulations incorporating a 1 mm vent (providing passive occlusion reduction) predict a combined active and passive occlusion reduction of 20 dB. A prototype occlusion canceling system was constructed. Averaged across 12 listeners with normal hearing, it provided 15 dB of occlusion reduction. Ten of the subjects reported a more natural own voice quality and an appreciable increase in comfort with the cancellation active, and 11 out of the 12 preferred the active system over the passive system. 相似文献
36.
Stuart J. Corr Lisa O'Reilly Eoghan P. Dillon Andrew R. Barron Patrick J. McNally 《Journal of Raman spectroscopy : JRS》2011,42(12):2085-2088
Poly(vinylpyrrolidone)‐stabilized silver nanoparticles deposited onto strained‐silicon layers grown on graded Si1−xGex virtual substrates are utilized for selective amplification of the Si–Si vibration mode of strained silicon via surface‐enhanced Raman scattering spectroscopy. This solution‐based technique allows rapid, highly sensitive and accurate characterization of strained silicon whose Raman signal would usually be overshadowed by the underlying bulk SiGe Raman spectra. The analysis was performed on strained silicon samples of thickness 9, 17.5 and 42 nm using a 488 nm Ar+ micro‐Raman excitation source. The quantitative determination of strained‐silicon enhancement factors was also made. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
37.
Megan L. Qualls Dr. Jinchao Lou Dillon P. McBee Prof. Joshua A. Baccile Prof. Michael D. Best 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(45):e202201164
Liposomes are effective therapeutic delivery nanocarriers due to their ability to encapsulate and enhance the pharmacokinetic properties of a wide range of therapeutics. Two primary areas in which improvement is needed for liposomal drug delivery is to enhance the ability to infiltrate cells and to facilitate derivatization of the liposome surface. Herein, we report a liposome platform incorporating a cyclic disulfide lipid (CDL) for the dual purpose of enhancing cell entry and functionalizing the liposome membrane through thiol-disulfide exchange. In order to accomplish this, CDL-1 and CDL-2 , composed of lipoic acid (LA) or asparagusic acid (AA) appended to a lipid scaffold, were designed and synthesized. A fluorescence-based microplate immobilization assay was implemented to show that these compounds enable convenient membrane decoration through reaction with thiol-functionalized small molecules. Additionally, fluorescence microscopy experiments indicated dramatic enhancements in cellular delivery when CDLs were incorporated within liposomes. These results demonstrate that multifunctional CDLs serve as an exciting liposome system for surface decoration and enhanced cellular delivery. 相似文献
38.
Jinchao Lou Megan L. Qualls Macy M. Hudson Dillon P. McBee Prof. Joshua A. Baccile Prof. Michael D. Best 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(46):e202201057
We report boronate-caged guanidine-lipid 1 that activates liposomes for cellular delivery only upon uncaging of this compound by reactive oxygen species (ROS) to produce cationic lipid products. These liposomes are designed to mimic the exceptional cell delivery properties of cell-penetrating peptides (CPPs), while the inclusion of the boronate cage is designed to enhance selectivity such that cell entry will only be activated in the presence of ROS. Boronate uncaging by hydrogen peroxide was verified by mass spectrometry and zeta potential (ZP) measurements. A microplate-based fluorescence assay was developed to study the ROS-mediated vesicle interactions between 1 -liposomes and anionic membranes, which were further elucidated via dynamic light scattering (DLS) analysis. Cellular delivery studies utilizing fluorescence microscopy demonstrated significant enhancements in cellular delivery only when 1 -liposomes were incubated with hydrogen peroxide. Our results showcase that lipid 1 exhibits strong potential as an ROS-responsive liposomal platform for targeted drug delivery applications. 相似文献
39.
Jonathan R. Carney Barry R. Dillon Leonie Campbell Dr. Stephen P. Thomas 《Angewandte Chemie (International ed. in English)》2018,57(33):10620-10624
The manganese‐catalyzed hydrosilylation and hydroboration of alkenes has been developed using a single manganese(II) precatalyst and reaction protocol. Both reactions proceed with excellent control of regioselectivity and in high yields across a variety of sterically and electronically differentiated substrates (25 examples). Alkoxide activation, using NaOtBu, was key to precatalyst activation and reactivity. Catalysis was achieved across various functional groups and on gram‐scale for both the developed methodologies with catalysts loadings as low as 0.5 mol %. 相似文献
40.