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151.
Wolfgang M. Weigert Heribert Offermanns Paul Scherberich Degussa 《Angewandte Chemie (International ed. in English)》1975,14(5):330-336
The non-naturally occurring amino acid D -penicillamine, originally only of interest as a key substance in the structural elucidation and total synthesis of penicillins is gaining increasing importance as a therapeutic, particularly in the long-term treatment of rheumatoid arthritis. D -Penicillamine which previously was obtained semi-synthetically by degradation of penicillins can now be totally synthesized using a new process which starts from isobutyraldehyde, sulfur, ammonia, and hydrogen cyanide and yields the racemate which is then selectively resolved. The biochemical behavior of D -penicillamine—chelate formation with heavy metal ions, cleavage of disulfide bridges, and condensation with aldehyde groups—affords information related to its therapeutic activity. 相似文献
152.
Klaus G. Heumann und Heribert Seewald 《Fresenius' Journal of Analytical Chemistry》1985,320(5):493-497
Zusammenfassung Es wurde ein Verfahren entwickelt, welches es erlaubt, in den verschiedenartigsten Wasserproben Spuren von Cl–, Br– und I– innerhalb einer Probenauf arbeitung durch massenspektrometrische Isotopenverdünnungstechnik zu bestimmen. Dabei hat diese definitive Methode den Vorteil, daß sie vergleichsweise richtige Analysenergebnisse liefert, weshalb sie sich vor allem auch als Eichmethode eignet. Am Beispiel von Talsperren-, Quell-, Flußund Mineralwasser wird die Anwendbarkeit des Verfahrens gezeigt. Dabei werden relative Standardabweichungen für die Chloridbestimmung im unteren ppm-Bereich von 0,2–2 1,6%, für die Analyse von Bromid und Iodid im unteren ppb-Bereich von 0,5–5% erreicht. Die Nachweisgrenze des Verfahrens, die durch genauere Isotopenverhältnismessungen noch verbesserungsfähig ist, liegt momentan bei 13 ppb für Cl–, bei 0,4 ppb für Br– und bei 0,1 ppb für I–. Ein analytischer Vergleich der Chloridbestimmung zeigt gute Übereinstimmung der massenspektrometrischen Ergebnisse mit denjenigen der Ionen-Chromatographie. Zusätzlich wird an einem Beispiel auch ein Verfahren erläutert, welches die Bestimmung der anorganischen Iodspezies Iodid und Iodat in Wässern durch massenspektrometrische Isotopenverdünnungsanalyse erlaubt.
Vortrag anläßlich des Symposiums Anorganische Anionenanalytik, Regensburg, 19.–21. 9. 1984
Diese Arbeit wurde im Rahmen des DFG-Schwerpunktprogramms Hydrogeochemische Vorgänge im Wasserkreislauf in der ungesättigten und gesättigten Zone finanziell unterstützt.Herrn Prof. G. Schwedt, Stuttgart, und Herrn Prof. K. H. Wedepohl, Göttingen, danken wir für die gute Zusammenarbeit bei der Bearbeitung dieses Teilthemas im Rahmen des Schwerpunktprogramms. 相似文献
Simultaneous determination of Cl–, Br– and I– in water samples by isotope dilution mass spectrometry
Summary An analytical procedure was developed which allows the trace determination of Cl–, Br– and I– in different water samples by isotope dilution mass spectrometry within a single reprocessing of the sample. This definitive method has the advantage that the analytical results are relatively accurate. Therefore, this type of analysis is especially suitable as a calibration method. Its application is shown by analysing water samples from a drinking water reservoir, different springs, river and a mineral water. The relative standard deviation for the chloride determination in the lower ppm-range is 0.2–1.6%, for the bromide and iodide analysis in the lower ppb-range it is 0.5–5%. The detection limits of this method — which could be improved by a more precise isotope ratio measurement — are 13 ppb for Cl–, 0.4 ppb for Br– and 0.1 ppb for I–. An analytical comparison for the chloride determination shows good agreement between the mass spectrometric method and ion chromatography. Additionally, an analysis procedure is given which allows the determination of the inorganic iodine species iodide and iodate in water samples by isotope dilution mass spectrometry.
Vortrag anläßlich des Symposiums Anorganische Anionenanalytik, Regensburg, 19.–21. 9. 1984
Diese Arbeit wurde im Rahmen des DFG-Schwerpunktprogramms Hydrogeochemische Vorgänge im Wasserkreislauf in der ungesättigten und gesättigten Zone finanziell unterstützt.Herrn Prof. G. Schwedt, Stuttgart, und Herrn Prof. K. H. Wedepohl, Göttingen, danken wir für die gute Zusammenarbeit bei der Bearbeitung dieses Teilthemas im Rahmen des Schwerpunktprogramms. 相似文献
153.
Thomas Falck Heribert Baldus Javier Espina Karin Klabunde 《Mobile Networks and Applications》2007,12(2-3):143-153
Wireless medical body sensors are a key technology for unobtrusive health monitoring. The easy setup of such wireless body area networks is crucial to protect the user from the complexity of these systems. But automatically forming a wireless network comprising all sensors attached to the same body is challenging. We present a method for making wireless body-worn medical sensors aware of the persons they belong to by combining body-coupled with wireless communication. This enables a user to create a wireless body sensor network by just sticking the sensors to her body. A personal identifier allows sensors to annotate their readings with a user ID thereby ensuring safety in personal healthcare environments with multiple users. 相似文献
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158.
Aggelos Avramopoulos Heribert Reis Josep M. Luis Manthos G. Papadopoulos 《Journal of computational chemistry》2013,34(17):1446-1455
The vibrational (hyper)polarizabilities of some selected Xe derivatives are studied in the context of Bishop–Kirtman perturbation theory (BKPT) and numerical finite field methodology. It was found that for this set of rare gas compounds, the static vibrational properties are quite large, in comparison to the corresponding electronic ones, especially those of the second hyperpolarizability. This also holds for the dc‐Pockels β(?ω;ω,0), Kerr γ(?ω;ω,0,0) and electric field second harmonic generation γ (?2ω;ω,ω,0) effects, although the computed nuclear relaxation (nr) vibrational contributions are smaller in magnitude than the static ones. HXeOXeH was used to study the effects of electron correlation, basis set, and geometry. Geometry effects were found to lead to noticeable changes of the vibrational and electronic second hyperpolarizability. A limited study of the effect of Xe insertion to the nr vibrational properties is also reported. Assessment of the results revealed that Xe insertion has a remarkable effect on the nr (hyper)polarizabilities. In terms of the BKPT, this is associated with a remarkable increase of the electrical and mechanical anharmonicity terms. The latter is consistent with the anharmonic character of several vibrational modes reported for rare gas compounds. © 2013 Wiley Periodicals, Inc. 相似文献
159.
Summary. Living cells, unicellular organisms as well as cells of multicellular organisms, are permanently exposed to a multitude of signals. Cells have to transform these external stimuli into physiological intelligible signals that are transduced from outside of the cell into the cell to induce a proper cellular response. Extracellular stimuli are perceived and internalised by various cellular receptors. Subsequently, signals are transduced by one of many protein kinase signaling cascades. Mitogen-activated protein kinases (MAPKs) belong to the evolutionary most conserved class of such molecular switches. MAPKs can change the activity of target proteins and thereby bring about physiological responses to external signals. This review discusses the basic principles of MAPK pathways in the context of cellular information processing: Cellular bioinformatics is an increasingly important interdisciplinary field with important implications for basic and applied sciences.Received February 24, 2003; accepted March 28, 2003
Published online August 18, 2003 相似文献
160.