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111.
A new chelating resin was prepared by coupling Amberlite XAD-2 with Brilliant Green through an azo spacer. The resulting resin has been characterized by FTIR spectrometry, elemental analysis, and thermogravimetric analysis and studied for the preconcentration and determination of trace Pb(II) ions from solution samples. The anionic complex of Pb(II) and iodide was retained on the resin by the formation of an ion associate with Brilliant Green on Amberlite XAD-2 in weak acidic medium. The optimum pH value for sorption of the metal ion was 5.5. The sorption capacity of the functionalized resin is 53.8 mg/g. The chelating resin can be reused for 20 cycles of sorption-desorption without any significant change in sorption capacity. A recovery of 103% was obtained for the metal ion with 0.1 M EDTA as the eluting agent. Scatchard analysis revealed that the homogeneous binding sites were formed in the polymers. The resin was subjected to evaluation through batch binding and column chromatography of Pb(II). The equilibrium adsorption data of Pb(II) on modified resin were analyzed by Langmuir, Freundlich, and Temkin models. Based on equilibrium adsorption data, the Langmuir, Freundlich, and Temkin constants were determined to be 0.192, 13.189, and 3.418 at pH 5.5 and 25 degrees C. The method was applied for lead ion determination in tap water samples.  相似文献   
112.
Computational studies have been carried out at the DFT-B3LYP/6-31G(d) level of theory on the structural and spectroscopic properties of 2-(1-oxo-1 H-inden-3-yl)-2H-indene-1,3-dione (OID). Experimental studies were conducted on these parameters, including X-ray, FT-IR and 13C NMR spectroscopy. The optimized geometries of OID and its bonding characteristics as well as IR and NMR spectra have been calculated and analyzed. It was observed that the bond lengths and angles in the molecule, obtained by X-ray, IR and NMR at the level of theory, were in a good agreement with those of the experiment. The correlation between the theoretical and the experimental vibrational frequencies and the chemical shifts of the OID molecule were 0.994 and 0.991, respectively. The agreement mutually verified the accuracy of the experimental method and the validity of the applied mathematical model.  相似文献   
113.
    
The development of new procedures for synthesizing new, low-cost, and stable metal oxides for the oxygen-evolution reaction (OER) by water oxidation is critical. Since the 2000s, there has been a rapid rise in the use of first-row transition metal (hydr)oxides for the OER. However, there is still a need to design and synthesize an efficient and stable catalyst for the OER. The present paper aims to design and synthesize an OER catalyst based on “a look at nature” strategy. In a simple and chemical evolution-like experiment, for the first time, a solution composed of various perchlorate cations, namely, Li(I), Mg(II), Ca(II), Al(III), Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Ba(II), and Na2SiO3, at a concentration of 1.0 mM at pH=4 and a potential of 1.40 V vs. NHE, which was under stirring for 15 days, was investigated. The stable OER catalyst on the electrode was characterized by X-ray absorption spectroscopy, scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. Based on the extrapolation of the Tafel plot, the onset of the OER in the presence of this catalyst was 130 mV lower than a bare electrode without it. This approach could be a roadmap to design and synthesize new and stable catalysts.  相似文献   
114.
Abstract: Aryl or alkyl propargyl ethers have been isomerized efficiently with good to excellent yield into corresponding allenyl ethers in the presence of potassium tert-butoxide under the microwave irradiation.  相似文献   
115.
An efficient and simple route is presented to the synthesis of some iminothiazolidinone derivatives. α‐Chloro amide derivatives undergo coupling reaction with isothiocyanate in the presence of a mild base, followed by nucleophilic substitution of chlorine by the sulfur atom of isothiocyanate.  相似文献   
116.
A new heterogeneous copper catalyst was synthesized by immobilization of copper ions onto magnetic nanoparticles with a new ligand based on triazole. The catalyst was characterized using scanning and transmission electron microscopies, atomic absorption and Fourier transform infrared spectroscopies, and thermogravimetric, elemental and energy‐dispersive X‐ray analyses. The results confirmed that a good level of organic groups was immobilized on the magnetic nanoparticles. Huisgen cycloaddition reaction was chosen as a model reaction for the investigation of catalyst activity under green conditions. Phenylacetylene and benzyl bromide derivatives were used for the synthesis of triazoles. The reaction proceeded with good to excellent yields for various alkynes and alkyl halides. To investigate catalyst activity for inactive alkynes, aliphatic alkynes were used in the model reaction. The corresponding triazoles were obtained in good to excellent yields and a high regioselectivity for products was obtained. The catalyst was easily separated using an external magnetic field and subsequently reused in ten reaction cycles without any loss of catalytic activity. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   
117.
Let v and be two varieties of groups defined by the sets of laws V and W, respectively. In this paper we construct a -v-covering group of a finite v-perfect group G, and show that every automorphism of G may be lifted to its -v-covering group. These generalize the previous work of the first two authors (1999). We also characterize the -v-irreducible extensions in some sense.AMS Mathematics Subject Classification (2000) Primary 20E34 20E36 Secondary 20E10  相似文献   
118.
In this paper we introduce the concept of Baer-invariant of a pair of groups with respect to a variety of groups v. Some inequalities for the Baer-invariant of a pair of finite groups are obtained, when v is considered to be the Schur-Baer variety. We also present a condition for which the order of the Baerinvariant of a pair of finite groups divides the order of the Baer-invariant of their factor groups. Finally, some inequalities for the Schur-multiplier of a pair of finite nilpotent groups and their factor groups are given.  相似文献   
119.
The present study investigates the effects of different concentrations, as well as type of plant growth regulators (PGRs) and medium (MS, Duchefa) on the growth and development of Centella asiatica in semi-solid culture. In addition, a protocol for successful sterilization of C.asiatica explants prepared from field-grown plants highly exposed to fungal and bacterial contamination was determined. Results for sterilization treatments revealed that applying HgCl? and Plant Preservative Mixture (PPM) with cetrimide, bavistin and trimethoprim which were included after washing with tap water, followed by the addition of PPM in the medium, produced a very satisfactory result (clean culture 90 ± 1.33%) and TS5 (decon + cetrimide 1% + bavistin 150 mg/L + trimethoprim 50 mg/L + HgCl?0.1% + PPM 2% soak and 2 mL/L in medium) was hence chosen as the best method of sterilization for C.asiatica. The synergistic combination of 6 benzylaminopurine (BAP) and 1-naphthaleneacetic acid (NAA) in concentrations of 2 mg/L and 0.1 mg/L, respectively, in Duchefa medium compared with MS induced the most optimal percentage of sprouted shoots (93 ± 0.667), number of shoots (5.2 ± 0.079) and nodes (4 ± 0.067) per explant, leaf per explant (14 ± 0.107) and shoot length (4.1 ± 0.67 cm). Furthermore, optimum rooting frequency (95.2 ± 0.81%), the number of roots/shoot (7.5 ± 0.107) and the mean root length (4.5 ± 0.133 cm) occurred for shoots that were cultured on full-strength MS medium containing 0.5 mg/L indole-3-butyric acid (IBA). In this study, the acclimatized plantlets were successfully established with almost 85% survival. The findings of this study have proven an efficient medium and PGR concentration for the mass propagation of C.asiatica. These findings would be useful in micropropagation and ex situ conservation of this plant.  相似文献   
120.
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