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131.
Nitrogen and sulfur nucleophiles, such as amines, thiophenols, and aminophosphanes, add to the triple bond of P-ethynyl-λ5-phosphazenes to give regio and diastereoselectively P-ethenyl-λ5-phosphazenes. An equally selective substitution reaction, occurring by an addition-elimination pathway, on bis(iminophosphoranyl)ethenes has been also achieved.  相似文献   
132.
介绍了在云母表面一种拉直λ-DNA-组蛋白复合物的新方法.借助原子力显微成像表明,该方法不但对裸λ-DNA的拉直效果较好,而且可以拉直不同浓度的DNA-组蛋白的复合物.利用此方法可以在单分子水平上研究DNA的复制、转录过程以及DNA-蛋白质相互作用.  相似文献   
133.
We prove the parametric versions of -weighted integral inequalities for differential forms satisfying the A-harmonic equation. These results can be considered as extensions of the classical inequalities for Sobolev functions.  相似文献   
134.
N(2,2,0)代数的(∈,∈∨q_(λ,μ))-模糊关联理想   总被引:1,自引:1,他引:0  
从以下几个方面对N(2,2,0)代数(∈,∈∨q_((λ,μ)))-模糊关联理想进行了详细的研究.首先,给出N(2,2,0)代数广义模糊关联理想概念和点态化(∈,∈∨q_((λ,μ)))-模糊关联理想概念,研究了两者之间的等价关系;其次,给出了(∈,∈∨q_((λ,μ)))-模糊关联理想若干等价刻画;再次,讨论了(∈,∈∨q_((λ,μ)))-模糊关联理想与(∈,∈∨q_((λ,μ)))-模糊理想之间的关系;最后,获得了(∈,∈∨q_((λ,μ)))-模糊关联理想交与并的相关性质.  相似文献   
135.
Abstract

Die Umsetzung einer Reihe von λ3P-Diazaphosphetidinonen, MeNC(:O)N(Me)PY (Y [dbnd] NEt2: 1, N(CH2)4; 2, NPh2; 3, OMe; 4, N(cyc)2; 5), mit Phenylazid wird beschrieben. Die dabei primär entstandenen 2-Phenylimino-λ4P-diazaphosphetidinone, MeNC(:O)N(Me)P(:NPh)Y sind mit Ausnahme des sterisch anspruchsvollen Dicyclohexylderivats, Y [dbnd] N(cyc)2; 12, unbeständig und dimerisieren rasch zu den entsprechenden Diazadiphosphetidinen, 7 und 9–11. Aus 7 bildet sich in Lösung unter Abspaltung von MeN[dbnd]C[dbnd]NMe das A4P, λ4P,λ5P-Diazadiphosphetidin 8. Die neuen Verbindungen 8–12 wurden analytisch, 1H-, 13C- und 31P-NMR-spektroskopisch sowie durch ihre Massenspektren charakterisiert. Darüber hinaus wurde von Verbindung 11 eine Röntgenstrukturanalyse durchgeführt. Das Molekül besitzt kristallographische zweizählige Symmetric. Die Geometrie am Phosphor ist verzerrt trigonal bipyramidal, mit P—N-Bindungslängen 173.9. 179.2 pm (axial) sowie 168.3, 168.7 pm (äquatorial).

Compounds involving the 1,3-dimethyl-1,3-diaza-2-phosphetidin-4-one framework: Synthesis of 1,3- dimethyl-2-phenylimino-l,3-diaza-2λ4-phosphetidin-4-one derivatives. X-ray crystal structure analysis of 4,6-dimethoxy-5,10-diphenyl-l,3,7,9-tetramethyl- 1,3,5,7,9,10-hexaaza-4λ5,6λ5-diphosphadispiro- [3.1.3.l]decan-2,8-dione.

The reactions of a series of λ3P-diazaphosphetidinones MeNC(:O)N(Me)PY (Y [dbnd] NEt2,; 1, N(CH2)4; 2, NPh2,; 3, OMe; 4, N(cyc)2; 5), with phenyl azide are described. The initially formed 2-phenylimino-λ4P-diazaphosphetidinones, MeNC(:O)N(Me)P(:NPh)Y, are. except for the bulky dicyclohexyl derivative 12, unstable and dimerize rapidly to the corresponding diazadiphosphetidines, 7 and 9–11. The λ4P,λ4P-diazadiphosphetidine 8 is formed from 7 in solution by elimination of MeN[dbnd]C[dbnd]NMe. The novel compounds 8–12 were characterized by analysis, n.m.r. and mass spectroscopy; additionally, an X-ray crystal structure analysis of 11 was carried out. The molecule possesses crystallographic twofold symmetry. The P-N bond lengths are 173.9, 179.2 pm (axial) and 168.3, 168.7 pm (equatorial).  相似文献   
136.
Capacitive Deionization (CDI) is an emerging technology with great potential applications. Most researchers view it as a viable water treatment alternative to reverse osmosis. This research reports the preparation and application of a carbon aerogel polypyrrole (CA-PPy) composite for the desalination of NaCl solution by the hybrid CDI method. The carbon aerogel (CA) was prepared from a Resorcinol / Formaldehyde precursor by the sol–gel method. The aerogel obtained from the sol–gel was then pyrolysed in a tube furnace to form CA. Polypyrrole (PPy) was prepared by the Oxidative chemical polymerisation of pyrrole, ferric chloride hexahydrate (oxidant), and sodium dodecyl sulfate (dopant). A composite of CA and PPy was then prepared and used to modify carbon electrodes. The CA-PPy composite was characterised to verify its composition, morphology, thermal properties, and functional groups. The electrochemical properties of the material were determined by Cyclic voltammetry (CV) and Electrochemical impedance spectroscopy (EIS) tests. The electrochemical tests were done using a GAMRY potentiostat electrochemical workstation, a 1.0 M KCl was used as the electrolyte, and the applied potential window was (-0.2 to + 0.6) V for the CV test. The EIS test was done with the same concentration of KCl electrolyte at an applied potential of 0.22 V and at a frequency range of (0.1 – 100, 000) Hz. The optimal specific capacitance of the CA is 115F/g, and that of the composite is 360.1F/g, they were both obtained at a scan rate of 5 mV/s. The CDI desalination study of the CA-PPy composite showed a salt adsorption capacity (SAC) of 10.10 mg/g (300 mg/L NaCl solution) – 15.7 mg/g (800 mg/L NaCl solution) at 1.2 V applied voltage. The salt recovery efficiency of the electrode material in the 300 mg/L solution is 27 %, in the 500 mg/L solution, it is 20.12 %, and in the 800 mg/L solution, it is 15.41 %. The electrode material also showed good electrochemical stability after nine cycles of ion adsorption/desorption study.  相似文献   
137.
本文研究了((∈),(∈)V(q)(λ,μ))-模糊正规子群的一些新的性质.利用反扩张原理获得了它的满同态像与同态原像的相关结果,丰富了文献[1]中有关((∈),(∈)V(q)(λ,μ))-模糊正规子群的研究结果.  相似文献   
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