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41.
    
Silica‐supported Preyssler nanoparticles (H14[NaP5W30O110])/SiO2 are used as a new and recyclable catalyst for the preparation of 1,3‐diaryl‐5‐spirohexahydropyrimidines via a one‐pot condensation of anilines, formaldehyde, and cyclohexanone.  相似文献   
42.
We introduce a hybrid proximal point algorithm and establish its strong convergence to a common solution of a proximal point of a lower semi-continuous mapping and a fixed point of a demicontractive mapping in the framework of a CAT(0) space. As applications of our new result, we solve variational inequality problems for these mappings on a Hilbert space. Illustrative example is given to validate theoretical result obtained herein.  相似文献   
43.
与星象函数有关的拟共形近于凸调和映射   总被引:1,自引:0,他引:1  
讨论了一类解析部分为星象函数的拟共形近于凸调和映射的基本性质,得到了此类映射的系数不等式、积分表达式、增长定理、面积定理与部分和的近于凸半径.  相似文献   
44.
A value of 74(+/-4) degrees was determined from NMR-observed dipolar couplings for the rotational dihedral angle of the monosuccinate anion in an aprotic liquid-crystal solution of the gauche conformation of tetraoctylammonium monosuccinate. This value is in reasonable agreement with other, somewhat less definitive, evidence gleaned from isotropic vicinal proton-proton couplings of the essentially completely gauche preference of the monosuccinate anion in tert-butyl alcohol and aprotic solvents, such as DMSO and THF, and quantum computations for the monoanion in THF.  相似文献   
45.
    
Twenty-four analogs based on triazinoindole bearing benzimidazole/benzoxazole moieties (1–25) were synthesized. Utilizing a variety of spectroscopic methods, including 1H-, 13C-NMR, and HREI-MS, the newly afforded compounds (1–25) were analyzed. The synthesized analogs were tested against urease enzyme (in vitro) as compared to the standard thiourea drug. All triazinoindole-based benzimidazole/benzoxazole analogs (1–25) exhibited moderate to excellent inhibition profiles, having IC50 values of 0.20 ± 0.01 to 36.20 ± 0.70 μM when evaluated under the positive control of thiourea as a standard drug. To better understand the structure–activity relationship, the synthesized compounds were split into two groups, “A” and “B.” Among category “A” analogs, analogs 8 (bearing tri-hydroxy substitutions at the 2,4,6-position of aryl ring C) and 5 (bearing di-hydroxy substitutions at the 3,4-position of aryl ring C) emerged as the most potent inhibitors of urease enzyme and displayed many times more potency than a standard thiourea drug. Besides that, analog 22 (which holds di-hydroxy substitutions at the 2,3-position of the aryl ring) and analog 23 (bearing ortho-fluoro substitution) showed ten-fold-enhanced inhibitory potential compared to standard thiourea among category “B” analogs. Molecular docking studies on the active analogs of each category were performed; the results obtained revealed that the presence of hydroxy and fluoro-substitutions on different positions of aryl ring C play a pivotal role in binding interactions with the active site of the targeted urease enzyme.  相似文献   
46.
This paper describes a new structure of left-handed metamaterial (LHM) based on parametric studies using Computer Simulation Technology (CST) software. The LHM structure is a combination of the modified square rectangular split ring (MSRR) and the capacitance loaded strip (CLS). In this paper, the parametric studies are used to see the effect of frequency and the negative value range of permeability (μ r ) and permittivity (ε r ) toward changes of LHM parameters. The changes in the dimension of MSSR and CLS affect the S 11 and S 21 of the LHM structure which will affect the values of permeability and permittivity. The values of permeability and permittivity were extracted from the reflection and transmission coefficient data. The studies proved that the LHM structure can be designed within the frequency range of interest.  相似文献   
47.
Treatment of indole with substituted aldehyde in the presence of equimolar amount of sodium bromate and sodium hydrogen sulfite mixture in water yielded corresponding substituted bis(indolyl)methanes in good yields. This provides a facile and environmentally friendly method towards the synthesis of an important class of organic compounds.  相似文献   
48.
Well-defined poly(4-vinylpyridine) (P4VP) was synthesised by nitroxide-mediated radical polymerization using the BlocBuilder MAMA-SG1. The controlled character of the polymerization was confirmed by kinetic measurements and linear increase of the molar mass with monomer conversion. Poly(4-vinylpyridine) terminated with SG1 was then used as macroinitiator and chain extended to form poly(4-vinylpyridine-b-methyl methacrylate) and poly(4-vinylpyridine-b-(methyl methacrylate-co-styrene)) block copolymers. These block copolymers spontaneously organized into spherical inverse micelles in THF with critical micelle concentrations of 0.1 mg/mL for poly(4VP190-b-MMA91) and 0.01 mg/mL for poly(4VP190-b-(MMA57-co-S18)) and sizes of 70 and 130 nm (DLS), respectively. The inverse micelles were loaded with copper(II)acetate leading to a slight increase in micelle size. The uniform structure of the inverse micelles was confirmed by FeSEM images, while the presence of copper in the micelle core was established by energy-dispersive X-ray spectroscopy (EDX) and FTIR spectroscopy.  相似文献   
49.
In this study, the Bonner sphere spectrometer (BSS) used for measurement of neutron spectra based a BF3 long counter. The most important problem for this system was a high count of scattered neutrons. This spectrometer was established by designed a new shadow cone with a smaller length and improved attenuation coefficient. Because of shortening the length of the shadow cone, distance of source and center of the sphere was decreased. Furthermore, external part of the thermal detector was covered with a suitable layer to reduce the contribution count of scattering neutrons. Experimental results show that BSS system with BF3 long cylindrical counter, applying the proper developments, can be used in neutron fluence spectrometry.  相似文献   
50.
A titrimetric and spectrophotometric methods for cerium(IV) determination have worked out. The first method relies upon the treatment of cerium(IV) solution with an excessive amount of iodide; the liberated iodine is extracted into chloroform, then reduced to iodide. The latter is iodometrically determined after 6- or 36-fold amplification. The spectropho-tometric finish is based upon the reaction of the titled ion with iron(II), in the presence of hexacyanoferrate(II), to form an intense prussian blue color suitable for the trace determination of cerium(IV) ion.  相似文献   
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