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131.
Various N-tosyl arylimines reacted with methyl vinyl ketone and ethyl vinyl ketone in the presence of ion-supported Ph3P A and B to give adducts, N-(2′-methylene-3′-oxo-1′-arylbutyl)-4-methylbenzenesulfonamides and N-(2′-methylene-3′-oxo-1′-arylpentyl)-4-methylbenzenesulfonamides, respectively, in good yields with high purity by simple diethyl ether extraction of the reaction mixture. Moreover, ion-supported Ph3P A and B could be repeatedly used for the same reaction to provide the corresponding adducts while maintaining good yields with high purity. 相似文献
132.
133.
Plasmon mode imaging of single gold nanorods 总被引:5,自引:0,他引:5
We have investigated two-photon-induced photoluminescence images and spectra of single gold nanorods by using an apertured scanning near-field optical microscope. The observed PL spectrum of single gold nanorod can be explained by the radiative recombination of the electron-hole pair near the X and L symmetry points. PL images reveal characteristic features reflecting an eigenfunction of a specific plasmon mode as well as electric field distributions around the nanorod. 相似文献
134.
135.
Abstract— Ionic species were detected electrically on flash excitation of chlorophyll α following rapid production of the triplet state of the pigment. The action spectrum of photocurrent agreed well with the absorption bands of the pigment in the visible region; the threshold for the formation of ionic species in acetonitrile was 1.8 eV. Oxygen gas introduced into the solution completely prevented the appearance of the triplet and ionic species. The latter are suggested to result from electron-transfer between the triplet pigments. Decay processes of the ionic species varied markedly with changes in the solvent polarity. Direct photo-ionization of the pigment could be observed by UV excitation in some non-polar solvents. 相似文献
136.
Substoichiometric extraction of uranyl ion in a synergic system of a chelating reagent and a neutral ligand is described. The system is based on a substoichiometric amount of 2-thenoyltrifluoroacetone (TTA) and an excess of tributylphosphate (TBP); this is compared with a system involving a substoichiometric amount of trioctylphosphine oxide and an excess of TTA. The reproducibility of the substoichiometric extraction is 0.46 or 0.62%, respectively. The former method is superior because extraction of uranyl ion with TBP alone is negligible. The method is applicable to > ca. 10 μg of uranium. 相似文献
137.
Dependent on the selection of the light sources employed, the photoinduced iodoperfluoroalkylation of a variety of unsaturated compounds takes place efficiently via a radical mechanism. Upon irradiation with a xenon lamp through Pyrex (hnu >300 nm), terminal alkenes (R-CH=CH2) and alkynes (R-C triple bond CH) undergo iodoperfluoroalkylation with perfluoroalkyl iodides (RF-I) regioselectively, providing R-CH(I)-CH2-RF and R-C(I)=CH-RF, respectively. In the case of terminal allenes (R-CH=C=CH2), the photoinduced iodoperfluoroalkylation occurs selectively at the terminal double bond, giving the corresponding beta-perfluoroalkylated vinylic iodides (R-CH=C(I)-CH2-RF) in good yields. The photoinitiated reaction of vinylcyclopropanes (c-C3H5-C(R)=CH2) with RF-I proceeds via the rearrangement of cyclopropylcarbinyl radical intermediates to the homoallylic radical intermediates, and the corresponding 1,5-iodoperfluoroalkylated products (I-(CH2)2CH=C(R)-CH2-RF) are obtained in high yields. Isocyanides (R-NC), as C-N unsaturated compounds, also undergo the xenon-lamp-irradiated iodoperfluoroalkylation to provide the corresponding 1,1-adducts (R-N=C(I)-RF) in good yields. Furthermore, the present photoinitiation procedure can be applied to the iodotrifluoromethylation of unsaturated compounds, when the xenon-lamp-irradiated reactions are conducted under the refluxing conditions of excess CF3-I. 相似文献
138.
Two efficient and practical methods of synthesis of the C-10 substituent of DV-7751 (1), a novel quinolone carboxylic acid, were established. The first method utilizes an optical resolution of racemic 8-amino-6-benzyl-6-azaspiro[3.4]octane (13), while the second employs an enantioselective microbial reduction of 6-benzyl-5,8-dioxo-6-azaspiro[3.4]octane (8b). The enantiomeric excess of (S)-8-amino-6-benzyl-6-azaspiro[3.4]octane (11) with each method of synthesis is greater than 96%. 相似文献
139.
Nagahara T Imura K Okamoto H Oguro A Imahori H 《The journal of physical chemistry. B》2005,109(42):19839-19844
We fabricated porphyrin thin films on mica surfaces from acidic aqueous solutions of the preorganized H-aggregates of amphiphilic porphyrins by the simple spin-coating method. The morphological and spectroscopic properties of the film were investigated by scanning near-field optical microscopy. The results obtained in this study demonstrate that the preorganized structure in solution can be transferred as a thin film with a thickness of the monolayer level without losing their substantial structure and photophysical properties. 相似文献
140.
We have investigated optical properties of single gold nanorods by using an apertured-type scanning near-field optical microscope. Near-field transmission spectrum of single gold nanorod shows several longitudinal surface plasmon resonances. Transmission images observed at these resonance wavelengths show oscillating pattern along the long axis of the nanorod. The number of oscillation increases with decrement of observing wavelength. These spatial characteristics were well reproduced by calculated local density-of-states maps and were attributed to spatial characteristics of plasmon modes inside the nanorods. Dispersion relation for plasmons in gold nanorods was obtained by plotting the resonance frequencies of the plasmon modes versus the wave vectors obtained from the transmission images. 相似文献