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排序方式: 共有186条查询结果,搜索用时 671 毫秒
71.
Sibel Morkoç Karadeniz Tuba Klnç Burcu Bozkurt rak Tuba Irmak Sakaolu ar rak Mehmet Erturul Ali Ercan Ekinci 《光谱学与光谱分析》2016,36(6):1998-2000
In this Study, Cadmium Oxide (CdO) nanostructures were synthesized by using Chemical Bath Deposition Technique. The synthesized process was carried out at room temperature. The structural and optical properties of nanostructures was characterized by XRD, SEM and UV-Vis techniques. As a result, the CdO nanostructures are oriented along (111) plane of cubic crystal structure. The morphology of CdO nanostructures showed interconnected prism-like and cauliflower-type cluster nanostructure. The UV results of this structures with high absorbtion coefficient are observed to be in accordance with the CdO nanoparticles. 相似文献
72.
73.
B. C. Cetin J. Barhen J. W. Burdick 《Journal of Optimization Theory and Applications》1993,77(1):97-126
A new method for unconstrained global function optimization, acronymedtrust, is introduced. This method formulates optimization as the solution of a deterministic dynamical system incorporating terminal repellers and a novel subenergy tunneling function. Benchmark tests comparing this method to other global optimization procedures are presented, and thetrust algorithm is shown to be substantially faster. Thetrust formulation leads to a simple stopping criterion. In addition, the structure of the equations enables an implementation of the algorithm in analog VLSI hardware, in the vein of artificial neural networks, for further substantial speed enhancement.This work was supported by the Department of Energy, Office of Basic Energy Sciences, Grant No. DE-A105-89-ER14086. 相似文献
74.
Determination of vigabatrin in human plasma and urine by high-performance liquid chromatography with UV-Vis detection 总被引:1,自引:0,他引:1
A simple and reliable high-performance liquid chromatographic (HPLC) method with UV-Vis detection has been developed and validated for the determination of vigabatrin (VG) in human plasma and urine. The samples were pre-column derivatizated with 1,2-naphthoquinone-4-sulphonic acid sodium salt (NQS). A good chromatographic separation was achieved on a C18 column with a mobile phase consisting of acetonitrile and 10 mM orthophosphoric acid (pH 2.5) gradient elution. Tranexamic acid was used as an internal standard (I.S.). The method was linear over the concentration range of 0.8-30.0 microg/ml for both samples. The method is precise (relative standard deviation (R.S.D.) <9.13%) and accurate (relative mean error (RME) <-8.75%); analytical recoveries were 81.07% for plasma and 83.05% for urine. The assay was applied to pharmacokinetic study in a healthy volunteer after a single oral administration of 1 g of vigabatrin. 相似文献
75.
A manganese(III) complex of tetraphenylporpholactone, Mn(TPPL)Cl, was synthesized and characterized, including by single-crystal X-ray diffraction; the catalytic activity of this complex for olefin epoxidation reactions is compared with that of manganese(III) tetraphenylporphyrin chloride, Mn(TPP)Cl. 相似文献
76.
Celik SU Akbey U Graf R Bozkurt A Spiess HW 《Physical chemistry chemical physics : PCCP》2008,10(39):6058-6066
The synthesis, thermal and proton conducting properties of copolymers based on vinylphosphonic acid (VPA) and 1-vinyl-1,2,4-triazole (VTri) were investigated. The copolymers were synthesized by free-radical copolymerization of the corresponding monomers at several monomer feed ratios to obtain poly(VPA-co-VTri) copolymer electrolytes. The final structures of the copolymers were confirmed by spectroscopic methods. The composition of the low molecular weight copolymers was varied with the feed ratio of the monomers. The presence of triazole units in the copolymers suppresses the formation of phosphonic acid anhydrides up to 150 degrees C, as verified by both (31)P NMR and TGA. The observation of defined glass transition temperatures indicated that the ionic interactions do not prevent segmental relaxations of the polymer chains. In the absence of humidity, the copolymer electrolyte, poly(VPA-co-VTri), S2 (with 33% triazole content) showed proton conductivity of 10(-3) S cm(-1) at 120 degrees C, which is far higher than in imidazole based copolymers. Two different types of hydrogen-bonded protons were detected by (1)H MAS NMR in the solid copolymer systems, due to different arrangements of triazole and phosphonic acid units. 相似文献
77.
Havva Nur Demirtas Selahattin Bozkurt Mustafa Durmaz Mustafa Yilmaz Abdulkadir Sirit 《Tetrahedron: Asymmetry》2008,19(17):2020-2025
Two novel chiral calix[4]azacrown ethers 4 and 5 bearing a furfuryl group on the nitrogen atom were developed by the reaction of dibromo- or ditosyl derivatives of p-tert-butylcalix[4]arenes 2 and 3 with a chiral diol, 1. The enantioselective recognition of these receptors towards the enantiomers of racemic carboxylic acids has been studied by 1H NMR spectroscopy. The molar ratio and the association constants of the chiral compounds 4 and 5 with each of the enantiomers of guest molecules were determined by using Job plots and a nonlinear least-squares fitting method, respectively. The Job plots indicate that both of the hosts form 1:1 instantaneous complexes with (R)- or (S)-mandelic acid and (l)- or (d)-dibenzoyltartaric acid. The receptors exhibited different chiral recognition abilities towards the enantiomers of racemic guests. 相似文献
78.
Milovanovi Emina Bozkurt Altinda erife Burcu Mateji Marjan Milovanovi Igor 《Czechoslovak Mathematical Journal》2022,72(3):783-799
Czechoslovak Mathematical Journal - Let a = (a1,a2, …, an) be a nonincreasing sequence of positive real numbers. Denote by S = {1, 2, …, n} the index set and by Jk = {I = {r1, r2,... 相似文献
79.
80.
C(2)-Symmetric two bis(amino alcohol)oxalamides (diamidediols) were synthesized and fully characterized. A new method was developed and successfully applied for the simultaneous preconcentration of both trace and toxic metals in water, by using C(2)-symmetric compounds. Under the optimum experimental conditions (i.e. pH = 10.0 +/- 0.2, 2.75 x 10(-3) mol L(-1) N,N'-bis[(1R)-1-ethyl-2-hydroxyethyl]ethanediamide (DAD1), 1.75 x 10(-3) mol L(-1) N,N'-bis[(1S)-1-benzyl-2-hydroxyethyl]-ethanediamide (DAD2), 0.10% w/v octylphenoxy-polyethoxyethanol (Triton X-114)), calibration graphs were linear in the range of 2.5 - 25.0 ng mL(-1) for Cu and Cd, 5.0 - 25.0 ng mL(-1) for Co and Ni. The enrichment factors were 18, 23, 18 and 20 for Cd, Cu, Co and Ni in the case of DAD1, respectively; 20, 22, 17 and 20 for Cd, Cu, Co and Ni in the case of DAD2. The limits of detection for DAD1 were found to be 0.45, 0.50, 1.25 and 0.60 ng mL(-1) for Cd, Cu, Co and Ni, respectively, and for DAD2 were found to be 0.44, 0.25, 0.60 and 1.55 ng mL(-1) for Cd, Cu, Co and Ni, respectively. The developed method was applied to the determination of Cu, Cd, Co and Ni in water samples and certified reference materials with satisfactory results. 相似文献