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151.
A. I. Akimenko N. M. Ponomarenko I. K. Yanson P. Samuely M. Reiffers 《Zeitschrift für Physik B Condensed Matter》1990,79(2):191-194
The electron-phonon interaction in LaNi5 is studied by point-contact spectroscopy. The spectrum corresponding to the electron-phonon interaction function g (the phonon density of states modulated by the matrix element of the electron-phonon interaction) is found. The functiong is used to analyze the point-contact spectra of PrNi5, where besides the electron-phonon contribution there is also an interaction between the conduction electrons and the crystal electric field levels of the Pr3+ ion. 相似文献
152.
The cationic ruthenium-hydride complex [(PCy3)2(CO)(CH3CN)2RuH]+BF4- (1) was found to be an effective catalyst for the regioselective coupling reaction of benzocyclic amines and terminal alkynes to form the tricyclic quinoline derivatives. The scope of the reaction was explored by using the catalytic system Ru3(CO)12/NH4PF6. The catalytically active cationic ruthenium-acetylide complex [(PCy3)2(CO)(CH3CN)2RuCCPh]+BF4- was isolated from the reaction of 1 with phenylacetylene. 相似文献
153.
Four new methyloxorhenium(V) compounds were synthesized with these tridentate chelating ligands: 2-mercaptoethyl sulfide (abbreviated HSSSH), 2-mercaptoethyl ether (HSOSH), thioldiglycolic acid (HOSOH), and 2-(salicylideneamino)benzoic acid (HONOH). Their reactions with MeReO(3) under suitable conditions led to these products: MeReO(SSS), 1, MeReO(SOS), 2, MeReO(OSO)(PAr(3)), 3, and MeReO(ONO)(PPh(3)), 4. These compounds were characterized spectroscopically and crystallographically. Compounds 1 and 2 have a five-coordinate distorted square pyramidal geometry about rhenium, whereas 3 and 4 are six-coordinate compounds with distorted octahedral structures. The kinetics of oxidation of 2 and 3 in chloroform with pyridine N-oxides follow different patterns. The oxidation of 2 shows first-order dependences on the concentrations of 2 and the ring-substituted pyridine N-oxide. The Hammett analysis of the rate constants gives a remarkably large and negative reaction constant, rho = -4.6. The rate of oxidation of 3 does not depend on the concentration or the identity of the pyridine N-oxide, but it is directly proportional to the concentration of water, both an accidental and then a deliberate cosolvent. The mechanistic differences have been interpreted as reflecting the different steric demands of five- and six-coordinate rhenium compounds. 相似文献
154.
Nelsen SF Konradsson AE Weaver MN Guzei IA Goebel M Wortmann R Lockard JV Zink JI 《The journal of physical chemistry. A》2005,109(48):10854-10861
Photolysis into the longest wavelength absorption band of 2-tert-butyl-2,3-diazabicyclo[2.2.2]oct-3-yl hydrazine (Hy) substituted naphthalenes causes aryl group reduction electron transfer to give (+)Hy-Ar(-). Electrooptical absorption measurements characterize the charge separation properties from these bands. Emission studies demonstrate that the separation between absorption and emission maxima for symmetrically disubstituted compounds is smaller than that for monosubstituted compounds, which is attributed to excited-state intervalence. The excited-state diabatic surfaces may be described as a Hy(+)-NA(- )-Hy(0), Hy(0)-NA(-)-Hy(+) pair, for which electronic interaction produces a double minimum that qualitatively resembles that in the ground state of the disubstituted intervalence radical cations. 相似文献
155.
Summary It was shown that (CF3CH2CH2)2SiCl2, along with Cl3SiCH2CH2CF3 and CH3Si(Cl)2CH2CH2CF3 may easily be prepared without danger by the addition of H2SiCl2 and HSiCl3 or CH2SiHCl2 in the presence of platinohydrochloric acid. 相似文献
156.
Chemistry of the aromatic 9-germafluorenyl dianion and some related silicon and carbon species 总被引:1,自引:0,他引:1
Liu Y Ballweg D Müller T Guzei IA Clark RW West R 《Journal of the American Chemical Society》2002,124(41):12174-12181
Dipotassio-9-germafluorenyl dianion (3b) was synthesized by reduction of 9,9-dichloro-9-germafluorene (4b) with sodium/potassium alloy in tetrahydrofuran. The X-ray crystal structure of 3b, like that for the analogous silicon compound 3a, shows C-C bond length equalization in the five-membered metallole rings and C-C bond length alternation in the six-membered benzenoid rings, indicating aromatic delocalization of electrons into the germole ring of 3b. Calculated nucleus independent chemical shift (NICS) values indicate that the five-membered ring is more aromatic than the six-membered rings in 3a and 3b. Derivatization of 3b with Me(3)SiCl gave 9,9-bis(trimethylsilyl)-9-germafluorene (5). Controlled oxidation of 3b yielded dipotassio-9,9'-digerma-9,9'-bifluorenyl dianion (6). Reaction of 6 with MeOH yielded 9,9'-digerma-9,9'-bifluorene (7). The X-ray structure of 6 indicates C-C bond length alternation in the five-membered rings. Thus dianion 6, like its silicon analogue 8, has the negative charges localized at metal atoms and no aromatic character. Dipotassio-9,9'-bifluorenyl dianion (9), the carbon analogue of 6, exhibits aromaticity with its X-ray crystal structure showing the C-C bond length equalization in both the five- and six-membered rings. Derivatization of 9 with MeI gave 9,9'-dimethyl-9,9'-bifluorene (10). The structure of 10 shows that the two fluorenyl rings are cis to each other with a torsional angle of 59 degrees and a long C-C single bond (1.60 A) connecting them. 相似文献
157.
V. V. Il'in O. V. Slavinskaya Yu. A. Strelenko A. V. Ignatenko V. A. Ponomarenko 《Russian Chemical Bulletin》1991,40(11):2177-2180
Previously unknown 1,4-dichloro-1,4-bis(perfluoroalkyl)-1,3-diazatetra-1,3-Dienes have been prepared and shown to be mixtures of isomers of Z and E configurations. The structures have been identified and a quantitative estimate made of the ratio of Z and E isomers using13C,19F, and15N NMR spectroscopy. 相似文献
158.
Denisov IG McLean MA Shaw AW Grinkova YV Sligar SG 《The journal of physical chemistry. B》2005,109(32):15580-15588
The role of lipid domain size and protein-lipid interfaces in the thermotropic phase transition of dipalmitoylphosphatidylcholine (DPPC) and dimyristoylphosphatidylcholine (DMPC) bilayers in Nanodiscs was studied using small-angle X-ray scattering (SAXS), differential scanning calorimetry (DSC), and generalized polarization (GP) of the lipophilic probe Laurdan. Nanodiscs are water-soluble, monodisperse, self-assembled lipid bilayers encompassed by a helical membrane scaffold protein (MSP). MSPs of different lengths were used to define the diameter of the Nanodisc lipid bilayer from 76 to 108 A and the number of DPPC molecules from 164 to 335 per discoidal structure. In Nanodiscs of all sizes, the phase transitions were broader and shifted to higher temperatures relative to those observed in vesicle preparations. The size dependences of the transition enthalpies and structural parameters of Nanodiscs reveal the presence of a boundary lipid layer in contact with the scaffold protein encircling the perimeter of the disc. The thickness of this annular layer was estimated to be approximately 15 A, or two lipid molecules. SAXS was used to measure the lateral thermal expansion of Nanodiscs, and a steep decrease of bilayer thickness during the main lipid phase transition was observed. These results provide the basis for the quantitative understanding of cooperative phase transitions in membrane bilayers in confined geometries at the nanoscale. 相似文献
159.
M. M. Davtyan S. P. Krukovskii A. V. Ignatenko V. A. Ponomarenko 《Russian Chemical Bulletin》1977,26(12):2575-2577
Conclusions It was found that exchange reaction takes place between N-(perfluorobutyrylimidoyl)perfluoropropyl-amidine and N-(perfluoro-2-methyl-3-oxahexylimidoyl)perfluoro-2-methyl-3-oxahexylamidine at temperatures where their thermal condensation to triazines still does not take place.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2784–2787, December, 1977. 相似文献
160.