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21.
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C. Sekar S. PaulrajG. Krabbes M. KanagarajS. Arumugam Ravhi S. Kumar 《Journal of magnetism and magnetic materials》2011,323(23):3033-3037
MCu2O3 (M=Ca and Co) system has two-leg spin ladder structure similar to that of the prototype SrCu2O3 system except that the rungs are buckled with an angle of 123° and 105° for CaCu2O3 and CoCu2O3 compounds, respectively. We have synthesized powder samples of (Ca1−xCox)Cu2O3 (x=0.00-1.00) by the solid state reaction method and their structural and magnetic properties have been investigated. All the synthesized compounds crystallize in orthorhombic structure with space group Pmmn. Lattice parameters of (Ca1−xCox)Cu2O3 decrease with the increase in Co content. DC magnetic susceptibility χ(T) results of the end products CaCu2O3 and CoCu2O3 show antiferromagnetic transition (TN) at 27 and 215 K, respectively. Co doping into (Ca1−xCox)Cu2O3 enhances its TN systematically with increasing Co concentration. The χ(T) of CoCu2O3 shows a broad transition with the peak temperature around 215 K and it was found to be field independent up to 90 kOe. The ambiguity concerning the transition was ruled out by recording the temperature dependent X-ray diffraction pattern on CoCu2O3 system, which indicated that there is no structural transition in the investigated temperature range of 115-300 K. Further, specific heat measurement on CoCu2O3 confirms the magnetic phase transition by the appearance of a sharp peak at 215 K. 相似文献
23.
A. Abdul Ajees K. Sekar S. Parthasarathy K. Balakrishna 《Crystal Research and Technology》2000,35(9):1117-1123
The crystal structure of the title compound has been determined from X‐ray diffraction. The compound crystallizes from benzene in the orthorhombic system, space group P212121, with unit cell parameters: a = 8.485(2), b = 9.816(2), c = 22.597(4) Å, Z = 4, V = 1881.9(7) Å3. The structure was determined by direct methods and refined to a final R‐factor of 0.04. Six membered rings B and E are planar. Ring A and ring C are in slightly distorted sofa conformation. Ring D is in envelope conformation. The structure is stabilised by weak intermolecular C‐H...O hydrogen bonds. 相似文献
24.
The occurrence of similar structural repeats in a protein structure has evolved through gene duplication. These repeats act as a structural building block and form more than one compact structural and functional unit called a repeat domain. The protein families comprising similar structural repeats are mainly involved in protein–protein interactions as well as binding to other ligand molecules. The identification of internal sequence repeats in the primary structure is not sufficient for the analysis of structural repeats. Thus, a new method called ProSTRIP has been developed using dynamic programming to find the similar structural repeats in a three-dimensional protein structure. The detection of these repeats is made by calculating the protein backbone Cα angles. An internet computing server is also created by implementing this method and enables graphical visualization of the results. It can be freely accessed at http://cluster.physics.iisc.ernet.in/prostrip/. 相似文献
25.
A series of optically active cyclic trans-β-aryloxy alcohols have been obtained by non-enzymatic kinetic resolution of the corresponding racemic aryloxy cyclic alcohols using commercially available (S)-BINAP and NCS by SN2 halogenation of a hydroxy group. The product, cis-β-aryloxy chlorides, was also obtained in optically active form with inversion of the stereochemistry. 相似文献
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27.
Synthesis,Characterization, and Antibacterial Activity of Novel (1H‐Benzo[d]imidazole‐2‐yl)‐6‐(diethylamino)‐3H‐one‐xanthene,Phenoxazine, and Oxazine 下载免费PDF全文
Vikas S. Patil Vikas S. Padalkar Kiran R. Phatangare Prashant G. Umape Bhushan N. Borase N. Sekar 《Journal of heterocyclic chemistry》2015,52(1):124-129
A series of novel (1H‐benzo[d]imidazole‐2‐yl)‐6‐(diethylamino)‐3H‐one‐xanthene, phenoxazine, and oxazine derivatives have been synthesized from 2‐(2′,4′‐dihydroxyphenyl) benzimidazole intermediate. Synthesized compounds 8a , 8b , 8c , 8d are fluorescent in solution, photophysical properties of compounds were studied and results revealed that compounds absorb and emit in UV–visible region with good fluorescence quantum yield. Synthesized compounds are thermally stable up to 300°C. The antibacterial activities of the synthesized compounds were studied by the well‐diffusion method. Escherichia coli (ATTC‐25922), Staphylococcus aureus (ATCC‐25923), Micrococcus (ATCC‐4698), and Bacillus subtilis (ATCC‐55422) were used to investigate the antibacterial activities. 相似文献
28.
An efficient Cu-catalyzed one-pot approach for the synthesis of unsymmetrical diaryl thioethers using potassium ethyl xanthogenate as a thiol surrogate is developed. This new protocol avoids usage of intricate thiols and makes use of its easily available xanthate as a precursor, and thiol will be generated in situ to prepare the diaryl thioethers through a Cu-catalyzed double arylation. This strategy was further successfully utilized for the synthesis of symmetrical diaryl thioethers, aryl alkyl thioethers, and benzothiazoles. 相似文献
29.
Copper crystals have been grown by Czochralski technique in a 6-bar argon gas environment. X-ray analysis shows that these
are single crystals and are strain-free. A slight pressure environment that is truly hydrostatic seems to improve the quality
of the crystals. Thermal profile estimation results show that the values of temperature which decrease upto the neck region
are same in magnitude as those measured during the experiments and that necking improves the thermal profile and, consequently,
the crystal quality. No facet formation has been observed in these crystals. 相似文献
30.
The double layer like potential jumps have been observed in a double plasma device. They do not correspond to a switching
of plasma potential from one metastable state to another but are caused by the ionisation of a very minute amount of the gas
that inevitably leaks into the system during the probe movement. 相似文献