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71.
We shall show how the nilpotency class of a finite loop Q is determined by the properties of a nilpotent inner mapping group. We also show that a classical result by Baer on the structure of abelian finite capable groups holds for Moufang loops of odd order.  相似文献   
72.
Four titanium complexes derived from 2-(2-ethylanilino)-, 2-(3,5-dimethylanilino)pyridine, 2-(4-n-butylanilino)- and 2-(2-t-butylanilino)pyridine were synthesized and characterized by spectroscopic methods. These complexes were used to catalyze the polymerization of ethylene in the presence of MAO as cocatalyst. The effect of the complex structures on the polymerization behavior was studied. All the alkylphenylaminopyridinato titanium complexes used in this study yielded higher molar masses than the unsubstituted bis(phenylaminopyridinato) titanium dichloride complex. Correspondingly, activities were lower and molar mass distributions were broader than those in the case of the unsubstituted bis(phenylaminopyridinato) titanium catalyst. The fluxional behavior of alkylphenylaminopyridinato titanium catalysts is probably the reason for the broad molar mass distributions. This might be due to the electron-donating effect from the alkyl substituent because the alkyl substituent enhances the active site isomerization rate.  相似文献   
73.
In addition to well-known dinuclear phenylselenolato palladium complexes, the reaction of [PdCl2(PPh3)2] and NaSePh affords small amounts of novel trinuclear and hexanuclear complexes [Pd3Se(SePh)3(PPh3)3]Cl (1) and [Pd6Cl2Se4(SePh)2(PPh3)6] (2). Complex 1 is triclinic, P1?, a=13.6310(2), b=16.2596(2), c=16.9899(3) Å, α=83.1738(5), β=78.9882(5), γ=78.7635(5)°. Complex 2 is monoclinic, C2/c, a=25.7165(9), b=17.6426(8), c=27.9151(14) Å, β=110.513(2)°. There are no structural forerunners for 1, but the hexanuclear complex 2 is isostructural with [Pd6Cl2Te4(TeR)2(PPh3)6] (R=Ph, C4H3S) that have been observed as one of the products in the oxidative addition of R2Te2 to [Pd(PPh3)4]. Mononuclear palladium complexes may play a significant role as building blocks in the formation of the polynuclear complexes.  相似文献   
74.
Two new imidazolate-bridged dinuclear CuII complexes, Na[Cu2(L1)2(im)] and K[Cu2(L2)2(im)] (where H2L1=6-amino-1,3-dimethyl-5(2-carboxyphenyl)azouracil and H2L2=1,3-dimethyl-5(2-carboxyphenyl)azobarbituric acid) have been prepared and characterized by magnetic susceptibility and spectroscopic measurements. Both compounds exhibit the expected antiferromagnetic behaviour with 2J=−54.8 and −30.4 cm−1, respectively. Because of the lack of suitable crystals for single crystal X-ray analysis, we have calculated the lowest energy structures using a program based on the MMX force field. On the basis of the results, the magnitude of the magnetic interaction is discussed. TMC 2623  相似文献   
75.
Vainio M  Halonen L 《Optics letters》2011,36(4):475-477
The frequency stability of a cw optical parametric oscillator (cw OPO) near the signal-idler degeneracy has been studied. The strong tendency of a near-degenerate OPO to mode hop has been suppressed by using a bulk Bragg grating as a spectral filter in the OPO cavity. An experimental demonstration of stable parametric oscillation in a single longitudinal mode of the OPO cavity is reported, together with the capability of tuning the signal-idler difference frequency from 1 to 4 THz. The OPO has potential use in cw terahertz generation.  相似文献   
76.
IR spectroscopy, laser induced fluorescence (LIF), and thermoluminescence (TL) measurements have been combined to monitor trapping, thermal mobility, and reactions of oxygen atoms in solid xenon. HXeO and O(3) have been used as IR active species that probe the reactions of oxygen atoms. N(2)O and H(2)O have been used as precursors for oxygen atoms by photolysis at 193 nm. Upon annealing of matrices after photolysis, ozone forms at two different temperatures: at 18-24 K from close O ...O(2) pairs and at approximately 27 K due to global mobility of oxygen atoms. HXeO forms at approximately 30 K reliably at higher temperature than ozone. Both LIF and TL show activation of oxygen atoms around 30 K. Irradiation at 240 nm after the photolysis at 193 nm depletes the oxygen atom emission at 750 nm and reduces the amount of HXeO generated in subsequent annealing. Part of the 750 nm emission can be regenerated by 266 nm and this process increases the yield of HXeO in annealing as well. Thus, we connect oxygen atoms emitting at 750 nm with annealing-induced formation of HXeO radicals. Ab initio calculations at the CCSD(T)/cc-pV5Z level show that XeO (1(1)Sigma(+)) is much more deeply bound [D(e) = 1.62 eV for XeO --> Xe+O((1)D)] than previous calculations have predicted. Taking into account the interactions with the medium in an approximate way, it is estimated that XeO (1(1)Sigma(+)) has a similar energy in solid xenon as compared with interstitially trapped O((3)P) suggesting that both possibly coexist in a low temperature solid. Taking into account the computational results and the behavior of HXeO and O(3) in annealing and irradiations, it is suggested that HXeO may be formed from singlet oxygen atoms which are trapped in a solid as XeO (1(1)Sigma(+)).  相似文献   
77.
SrS1−xSex and ZnS1−xSex thin films were deposited by the atomic layer deposition (ALD) technique using elemental selenium as the Se source, thus avoiding use of H2Se or organometallic selenium compounds. X-ray diffraction (XRD) analysis showed that the films were solid solutions and X-ray photoelectron spectroscopy (XPS) data showed that the surface of both ZnS1−xSex and SrS1−xSex were covered with an oxide and carbon-containing contaminants from exposure to air. The oxidation of SrS1−xSex extended into the film and peak shifts from sulfate were found on the surface. Luminance measurements showed that emission intensity of the ZnS1−xSex:Mn alternating current thin film electroluminescent (ACTFEL) devices at fixed voltage was almost the same as that of the ZnS:Mn device, while emission intensity of the SrS1−xSex:Ce devices decreased markedly as compared to the SrS:Ce device. Emission colors of the devices were altered only slightly due to selenium addition.  相似文献   
78.
Vinylcyclohexane (VCH) was copolymerized with ethene and propene using methylaluminoxane‐activated metallocene catalysts. The catalyst precursor for the ethene copolymerization was rac‐ethylenebis(indenyl)ZrCl2 ( 1 ). Propene copolymerizations were further studied with Cs‐symmetric isopropylidene(cyclopentadienyl)(fluorenyl)ZrCl2 ( 2 ), C1‐symmetric ethylene(1‐indenyl‐2‐phenyl‐2‐fluorenyl)ZrCl2 ( 3 ), and “meso”‐dimethylsilyl[3‐benzylindenyl)(2‐methylbenz[e]indenyl)]ZrCl2 ( 4 ). Catalyst 1 produced a random ethene–VCH copolymer with very high activity and moderate VCH incorporation. The highest comonomer content in the copolymer was 3.5 mol %. Catalysts 1 and 4 produced poly(propene‐co‐vinylcyclohexane) with moderate to good activities [up to 4900 and 15,400 kg of polymer/(mol of catalyst × h) for 1 and 4 , respectively] under similar reaction conditions but with fairly low comonomer contents (up to 1.0 and 2.0% for 1 and 4 , respectively). Catalysts 2 and 3 , both bearing a fluorenyl moiety, gave propene–VCH copolymers with only negligible amounts of the comonomer. The homopolymerization of VCH was performed with 1 as a reference, and low‐molar‐mass isotactic polyvinylcyclohexane with a low activity was obtained. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6569–6574, 2006  相似文献   
79.
We say that a near-ring (N,+,·) has an almost trivial multiplication (ATM) if the product of two elements belongs to the intersection of the additive cyclic groups generated by these two elements. We show that every finite near-ring with ATM can be decomposed to a direct sum where the summands are either near-rings defined on cyclic groups or near-rings whose minimal ideals are zero near-rings. Finally, we show how to construct these summands on cyclic groups.  相似文献   
80.
The HArF molecule can occupy in solid Ar thermally unstable and stable configurations, and their microscopic structure is not understood at the moment. We present additional experimental results on the formation of two HArF configurations and analyze them with emphasis on possible reactions of the unstable configuration with matrix vacancies to form the stable configuration. We conclude that the existing computational scenarios do not describe fully the present experimental data. In order to explain qualitatively the experimental results, two tentative models are discussed. The first model is based on local mobility of matrix vacancies produced during photolysis and the second model considers isomerization of the HArF at Arn supermolecule. More importantly, the present results constitute the experimental basis for future theoretical studies.  相似文献   
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