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441.
442.
M. Ganesan S. S. Krishnamurthy M. Nethaji K. Raghuraman 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1)
Abstract The reactions of chiral diphosphazanes. Ph2PN((S)-*CHMePh)PPhY (Y =Ph, N2C3HMe2-3,5) with [CpRu (PPh3)2Cl] and those of the monosulfides, Ph2PN(R)P(S)Ph2 (R = (S)-*CHMePh or CHMe2) with Ru3(CO)12. [RhCl(cod)]2 and [RhCI(CO)2]2 have been investigated. Molybdenum-palladium heterometallic complexes of the diphosphazanes, MeN(P(OR)2)2 (R = CH2CF3 or Ph) have been synthesised. Some unusual complexes have been obtained by the reductive carbonylation of cobalt and ruthenium halides in the presence of diphosphazanes, RN(PX2)2 (R = Me, X = OCH2CS or OPh; R = CHMe2, X = Ph). The structures of the products have been elucidated by NMR spectoscopy and in some cases confirmed by X-ray crystallography (e.g., 1–4). 相似文献
443.
K. A. Venkatesan K. Chandran N. Ramanathan S. Anthonysamy V. Ganesan T. G. Srinivasan 《Journal of Thermal Analysis and Calorimetry》2014,115(2):1979-1988
Thermal stability of neat octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (OΦD[IB]CMPO) and TRUEX solvent composition (0.2M OΦD[IB]CMPO-1.2M tri n-butyl phosphate-in n-dodecane) in the presence and absence of nitric acid has been studied in ambient air in a closed vessel, employing an adiabatic calorimeter. Enthalpies and kinetic parameters for the decomposition reaction were derived wherever possible and are reported for the first time. Neat OΦD[IB]CMPO was found to be thermally stable up to 633 K and exhibited an exothermic decomposition later. It decomposed at lower temperatures (376–386 K) depending on the nitric acid concentration. The exothermic rise in temperature and pressure increased exponentially, while activation energies exhibited exponential decrease for the decomposition reactions with increase in nitric acid content. TRUEX solvent was found to be stable up to 661 K in the absence of nitric acid while in the presence of 8 and 4M HNO3, it decomposed between 387 and 413 K. All these samples on decomposition formed incompressible gases and viscous black liquids. The results also indicate that the neat OΦD[IB]CMPO and the TRUEX solvent are thermally more stable than neat tri n-butyl phosphate (TBP), PUREX solvent (1.1M TBP/n-DD), neat diamyl amyl phosphonate (DAAP) and 1.1M DAAP/n-DD, triisoamyl phosphate (TiAP) and 1.1M TiAP/n-DD. 相似文献
444.
445.
Cyclic voltammetry and electrochemical impedance studies of Fe(tmphen) 3 2+ (where tmphen?=?3,4,7,8-tetramethyl-1,10-phenanthroline)-immobilized Nafion?-modified glassy carbon electrode (GC/Nf/Fe(tmphen) 3 2+ ) are carried out in 0.1?M Na2SO4 solution. Nafion–Fe(tmphen) 3 2+ complex exhibits efficient electrocatalytic oxidation of isoniazid. The linear double reciprocal plot of current and concentration of isoniazid shows a Michaelis–Menten-type catalytic process. The catalytic oxidation currents are proportional to the concentration of isoniazid and show a wide linear calibration range for the quantitative determination of isoniazid. Detection limit and sensitivity are found to be 13?μM and 2.5?μA?mM?1, respectively. 相似文献
446.
Fakhruddin Ahmed P. K. Gutch K. Ganesan R. Vijayaraghavan 《Journal of Thermal Analysis and Calorimetry》2012,107(1):141-147
N,N′-dichloro-bis[2,4,6-trichlorophenyl]urea, known as CC2, is used as a reactive chemical decontaminant of mustard agents. The
present study was undertaken to establish the compatibility of CC2 with a number of commonly used suspending agents, using
thermoanalytical techniques viz., thermogravimetry (TG) and differential scanning calorimetry (DSC) with the support of Fourier
transform infrared spectroscopy (FTIR). The results demonstrated the applicability of TG and DSC as a fast screening tool
for analysing the compatibility of drug with excipients at the early stages of a preformulation process. Methylcellulose,
hydroxypropylcellulose, and betaine were found to be compatible with CC2. 相似文献
447.
The [2 + 2] Schiff base condensation reactions between the newly synthesized dialdehyde, N,N-di(α-formylpyrrolyl-α-methyl)-N-methylamine), and ethylenediamine or p-phenylenediamine dihydrochloride readily afforded the 30- and 34-membered large size macrocycles in very high yields. Subsequent reduction reactions of these macrocycles with NaBH(4) gave the corresponding saturated macrocyclic hexaamines in good yields. The analogous reaction of the new dialdehyde with a triamine molecule afforded the [3 + 2] Schiff base macrobicycle in high yield, which was then reduced by reaction with NaBH(4) to give the saturated macrobicycle. All these compounds were characterized by spectroscopic methods. The anion binding properties of the saturated macrocycles having the ethylene and the phenylene linkers in CDCl(3) were studied by NMR titration methods. Although they have similar pyrrolic and amine NH groups their binding properties are different and interesting, owing to the conformational flexibility or rigidness rendered by the ethylene or phenylene groups, respectively. The macrocycle having the ethylene linkers binds anions in a 1:1 fashion, while the other receptor having the phenylene linkers prefers to bind anions in a sequential 1:2 fashion and has a multiple equilibria between a 1:1 and a 1:2 complexes, as shown by their binding constants, curve fittings by EQNMR, and Job plots. The X-ray structures of the 1:2 methanol, the aqua and the benzoate anion complexes of the macrocycles show two cavities in which the guests are bound, correlating with the high affinity found for the formation of stable 1:2 complexes in solution. The X-ray structure showed that the macrobicycle Schiff base adopts an eclipsed paddle-wheel shaped conformation and exhibits an out-out configuration at the bridgehead nitrogen atoms. 相似文献
448.
Vinu A Krithiga T Balasubramanian VV Asthana A Srinivasu P Mori T Ariga K Ramanath G Ganesan PG 《The journal of physical chemistry. B》2006,110(24):11924-11931
Iron substituted cubic cage type mesoporous molecular sieves (FeSBA-1) were synthesized for the first time in a highly acidic media using cetyltriethylammonium bromide as a template. The amount of Fe incorporation in SBA-1 can easily be controlled by the simple adjustment of the molar hydrochloric acid-to-silicon ratio. All the materials were unambiguously characterized by AAS, XRD, N2 adsorption, UV-Vis DRS, XPS, and ESR spectroscopy. The results from AAS, XRD, and N2 adsorption reveal that the iron atom can be incorporated in the framework of SBA-1 matrix without altering the structural order and the textural parameters. The nature and the coordination of iron atoms were extensively studied by XPS spectroscopy, and the results revealed that most of the iron atoms in FeSBA-1 are in +3 coordination state. UV-Vis DRS and ESR studies confirmed that the majority of the Fe atoms in FeSBA-1 exist in a tetrahedral coordination environment (most probably occupying framework positions). tert-Butylation of phenol employing tert-butanol as the alkylation agent was carried out over FeSBA-1 catalysts with different iron content and the results are compared with one-dimensional mesoporous catalysts. The influence of various reaction parameters such as reaction temperature, reactant feed ratio, weight hourly space velocity, and time-on-stream affecting the activity and selectivity of FeSBA-1 were also studied. Under the optimized reaction conditions, the FeSBA-1(36) catalyst showed superior catalytic performance for the tert-butylation of phenol as compared to the uni-dimensional mesoporous catalysts. 相似文献
449.
450.
We propose a continuum model for the dynamics of particles in polymer matrices which encompasses arbitrary size ratios of the polymer and particle. We present analytical and computer simulation results for the mobility of the particles and the viscosity of the suspension for the case of unentangled polymer melts. Our results indicate strong dependencies of the particle mobility upon the polymer-particle size ratios and much reduced intrinsic viscosities for the suspensions. These predictions rationalize some recent experimental observations on the dynamics of nanoparticles in polymer melts. 相似文献