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41.
Ebraheem Abdu Musad Saleh Abdullah Mohammed AL Dawsari Kakul Husain Ismail Hassan Kutty K.M.Lokanatha Rai 《Molecules (Basel, Switzerland)》2021,26(2)
A novel synthesis of thiazolo[2,3-b]quinazolines 4(a–e), pyrido[2′,3′:4,5]thiazolo[2,3-b]quinazolines {5(a–e), 6(a–e), and 7(a–e)}, pyrano[2′,3′:4,5]thiazolo[2,3-b]quinazolines 8(a–e), and benzo[4,5]thiazolo[2,3-b]quinazoloine9(a–e) derivatives starting from 2-(Bis-methylsulfanyl-methylene)-5,5-dimethyl-cyclohexane-1,3-dione 2 as efficient α,α dioxoketen dithioacetal is reported and the synthetic approaches of these types of compounds will provide an innovative molecular framework to the designing of new active heterocyclic compounds. In our study, we also present optimization of the synthetic method along with a biological evaluation of these newly synthesized compounds as antioxidants and antibacterial agents against the bacterial strains, like S. aureus, E. coli, and P. aeruginosa. Among all the evaluated compounds, it was found that some showed significant antioxidant activity at 10 μg/mL while the others exhibited better antibacterial activity at 100 μg/mL. The results of this study showed that compound 6(c) possessed remarkable antibacterial activity, whereas compound 9(c) exhibited the highest efficacy as an antioxidant. The structures of the new synthetic compounds were elucidated by elemental analysis, IR, 1H-NMR, and 13C-NMR. 相似文献
42.
Rosa L. Camacho-Mendoza Eliazar Aquino-Torres Julian Cruz-Borbolla Jose G. Alvarado-Rodríguez Oscar Olvera-Neria Jayanthi Narayanan Thangarasu Pandiyan 《Structural chemistry》2014,25(1):115-126
DFT studies of both the Fe4 cluster and the Fe(110) surface interaction with pyrrole, furan, thiophene, and selenophene showed that selenophene forms a stabler adsorbate iron complex than the other heterocyclic molecules; this is consistent with the binding energy data that were calculated between the Fe cluster and the Fe(110) surface with the heterocycles. Furthermore, when the adsorption of the compounds with the iron cluster was analyzed by molecular orbital studies, the orbitals of selenophene overlapped more strongly with the Fe atom than that of the other molecules. In TD-DFT, the π → π* peak observed for the molecules disappeared when they formed complexes, and there appeared a charge transfer band (ligand to metal), thus confirming the coordination of these molecules with the cluster. The data suggest that the chemisorption is an exothermic process. 相似文献
43.
Drop calorimetric measurements on a versatile monazite phase loaded with simulated radioactive waste
R. Asuvathraman Kitheri Joseph Jose Joseph M. V. Krishnaiah K. V. Govindan Kutty 《Journal of Thermal Analysis and Calorimetry》2014,117(3):1151-1156
Monazite is one of the candidate ceramic matrices for the immobilization of high level radioactive waste (HLW) from the reprocessing of spent nuclear fuel. The monazite phase, Ce0.8Ca0.2PO4, can accommodate cations of different valences due to the mixed valence state (+3 and +4) of Ce in this compound, by facilitating the oxidation and reduction of the Ce3+ and Ce4+ as required by the in-coming cation. This will assist in accommodating HLW of different compositions in the monazite crystal structure even if the average valence of the HLW elements is other than 3. Therefore, the monazite phase, Ce0.8Ca0.2PO4, can be a versatile host for the immobilization of HLW. The enthalpy increment and heat capacity of this versatile monazite phase and a simulated waste form based on it with 20 mass% HLW oxides were measured by drop calorimetry in the temperature range from 373 to 873 K, and the results are compared with those measured for CePO4. 相似文献
44.
Sustainable preparation of gold nanoparticles via green chemistry approach for biogenic applications
Novel premises of ‘Green Nanotechnology’ have tremendous impacts towards industrial scale revolution. The furtive extracted from natural precursors have driven to the generation of biogenic resources for the fabrication of cutting-edge nanomaterials in simple and cost-effective process. This inspection is an intension of the coupling hypothesis of Nanotechnology via ‘Green-Chemistry’ avenue. So, as to diminish the negative effects of technological applications in the health of human beings and the environment, society is focused towards a greener future. Nanoscience assures a promising future by its improvement in green chemistry to develop the 'Greenary Nanoscience and Nanotechnology'. The improvement and execution of chemical assisted processes in order to reduce the usage of harmful substances, the ‘Green Chemistry’ approach is one and only remarkable authentication, which attributed to long range surface area and higher pore volume of gold-nanoparticles. As of now, the efficient biogenic mechanism dramatically reduces the utilization and hazardous reagents have been employed to low-price natural and waste products to yield value-added nanomaterials with extensive relevance, suggesting an economical and green solution to environmental issues. In depth investigation of this critical review illustrates, novel biogenic screening platform was also conducted against antimicrobial strains and degradation of gold-nanoparticles products well explored-from selection precursors evolved from natural extracts, as well as eventually disintegration into bio-degradable yet potentially recyclable byproducts. 相似文献
45.
Monitoring the Transition from Spherical to Polymer‐like Surfactant Micelles Using Small‐Angle X‐Ray Scattering
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Dr. Grethe Vestergaard Jensen Dr. Reidar Lund Dr. Jérémie Gummel Dr. Theyencheri Narayanan Prof. Jan Skov Pedersen 《Angewandte Chemie (International ed. in English)》2014,53(43):11524-11528
Despite over a century of modern surfactant science, the kinetic pathways of morphological transitions in micellar systems are still not well understood. This is mainly as a result of the lack of sufficiently fast methods that can capture the structural changes of such transitions. Herein, a simple surfactant system consisting of sodium dodecyl sulfate (SDS) in aqueous NaCl solutions is investigated. Combining synchrotron radiation small‐angle X‐ray scattering (SAXS) with fast stopped‐flow mixing schemes allows monitoring the process where polymer‐like micelles are formed from globular micelles when the salt concentration is suddenly increased. The results show that “worm‐like” micelles are formed by fusion of globular micelles and short cylinders in a fashion that bears similarities to a step‐like polymerization process. 相似文献
46.
The enantioselective cyclization of the prochiral cyclic substrates1 to7 and26, can be carried out in theneat using S-proline as catalyst. The substrates18 to22 and27 could not be cyclized with S-proline but could be cyclized with a mixture of S-phenylalanine and d-camphorsulphonic acid.
The enantioselective cyclization of prochiral acyclic triones45 and47 and also the racemic tricarbonyl compounds54 to57 could also be carried out in theneat using S-proline as catalyst. The optically active enediones obtained in the above cyclizations could also be obtained directly
from 1,3-diones or 2-hydroxymethylene cycloalkanones in a one-pot reaction with methyl vinyl ketone (MVK) and S-proline in
the absence of solvents.13C NMR studies of the one-pot synthesis ofS-11 andS-14 reveal that the annulations involve initial formation of an acid-base complex followed by a Michael reaction and then an
enantioselective cyclization. Such enantioselective cyclizations probably occur on the surface of S-proline crystals. 相似文献
47.
We study fluctuations in the force at the boundary of a 2D granular flow. The forces are mainly impulsive at all flow rates. The probability distribution of impulses decays exponentially at large impulses, as do the forces in a static granular medium. At small impulses, the distribution evolves continuously with flow rate with no indication of the transition from collisional flow to intermittently jamming flows. However, the distribution of the time interval between collisions tends to a power law, P(tau) - tau(-3/2), showing a clear dynamical signature of the approach to jamming. 相似文献
48.
The modification of the extended 1 --> 3 anthraquinonoid monomer 1 by substitution of the central aliphatic moiety with a more rigid, aromatic moiety has allowed the syntheses of the new branched building block 6 possessing multiple, internal redox sites. This monomer was used to generate the first tier, dendritic macromolecules 8 and 9, which incorporate different internal redox centers within the infrastructure as well as the traditional peripheral multifunctionality. Using cyclic voltammetry experiments, the electrochemical response and electronic interactions between the two electroactive sites (the anthraquinonoid and nitroaromatic moieties) of these dendritic constructs were explored. 相似文献
49.
A.P.G. Kutty 《Journal of Physics and Chemistry of Solids》1984,45(1):121-125
The valence transition in SmS is investigated on the basis of a model which incorporates the Falicov-Kimball (F-K) interaction, f-d hybridization and electron-phonon interaction. We find that the transition is of first order even in the absence of electron-phonon interaction if the F-K interaction is sufficiently strong. Electron-phonon interaction makes the first order transition possible for a weaker F-K interaction. The effect is further enhanced if phonon-induced f-f and f-d coupling are simultaneously present. All calculations are done for finite temperature and the temperature dependence of the transition is found to be in agreement with the phase diagram of SmS. 相似文献
50.
The body of knowledge necessary to observe holographic-moiré patterns in real time is introduced. The basic factors influencing fringe visibility in holographic moiré are analyzed and expressions to evaluate fringe visibility for any given displacement and deformation are given. The application of the introduced theory in the case of real-time observation is discussed. It is shown that the maximum benefits of this technique are achieved by combining it with closed-circuit TV. Several examples of application are given. 相似文献