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881.
Toshio Kinoshita Yukihiro Watanabe Setsuko Nakao Sunao Furukawa 《Journal of heterocyclic chemistry》1992,29(7):1785-1788
The following 5-nitro-2,4(1H,3H)-pyrimidinediones possessing bromo substituted side chains at the 1- and 6-positions were prepared by bromination of 3,6-dimethyl-1-(ω-hydroxyalkyl)-5-nitro-2,4(1H,3H)-pyrimidinediones 4a and 4b and its nitrates 2a and 2b . The three of mono-bromo derivatives are: 1-(ω-acetoxyalkyl and ω-hydroxyalkyl)-6-bromomethyl-3-methyl. 6a, 6b, 7a and 7b and 1-(ω-bromoalkyl)-3,6-dimethyl-2,4(1H,3H)- pyrimidinediones 8a and 8b . The one type dibromo derivatives are: 1-(ω-bromoalkyl)-6-bromomethyl-3-methyl-2,4(1H,3H)-pyrimidinediones 5a and 5b . 相似文献
882.
M Yamashita T Miyazaki K Ohno M Fujita S Tanaka M Nakata A Watanabe K Okamoto N Tabata 《Radioisotopes》1983,32(4):167-170
Technetium-99m-diethylene-triamine-penta-acetic acid (DTPA) and 111In-DTPA were injected simultaneously into 21 patients with various levels of renal function. Scintiphoto, camera data renograms and clearance values (plasma sampling) were obtained for each patient. The mixed isotope scintiphoto images were of intermediate quality and the images with 111In-DTPA were apparently inferior to those with 99mTc-DTPA. These equations were obtained: (1) y = 0.30 + 0.91 x (coefficient of correlation r = 0.98) where x is the value at T peak (time of maximum count on renogram) obtained with 99mTc-DTPA and where y is the value at T peak with 111In-DTPA. (2) y = -0.09 + 1.006 x (r = 0.99) where x is the value at T3/4 (time interval between the time of maximum count to the time of 3/4 of maximum count on renogram) and where y is the value at T3/4 obtained with 111In-DTPA. (3) y = -0.01 + 1.007 x (r = 0.98) where the x and y values were for the excretion ratios (counts at 20 min/maximum counts on renogram). (4) y = 0.81 + 0.98 x (r = 0.99) where x and y are the clearance values. 相似文献
883.
T. Shinohara M. Fujioka H. Onodera K. Hisatake H. Yamamoto H. Watanabe 《Hyperfine Interactions》1975,1(1):345-360
From internal conversion experiments and the Mössbauer effect measurements, the 4s electron density and isomer shift for Fe impurity atoms in Cr, Ni, Cu, Pt and Au metals were studied. The M and N shell conversion electron spectra of the 14.4 keV transition of57Fe were measured using a high resolution β-ray spectrometer and analyzed using a deconvolution methods. The Mössbauer effect measurements were performed by a standard spectrometer with a moving absorber. Most of the samples showed isomer shift values consistent with the published ones. It is concluded that the 4s electron density, \(\rho _{4_S} (0)\) , at the nucleus of57Fe embedded is nearly equal in these host metals. The relation between \(\rho _{4_S} (0)\) and the isomer shift indicates that \(\rho _{3_S} (0)\) plays an important role in the variation of the isomer shift. 相似文献
884.
Hiroshi Watanabe 《Journal of statistical physics》1989,54(1-2):171-190
A block spin approach to the Euclidean
4 field theory in three dimensions is proposed by using the three-dimensional version of Gawedzki and Kupiainen's block spin transformation method. The lattice
3
4
model recovers the rotation invariance in the continuum limit, when the coupling constant is small. 相似文献
885.
886.
Suzuki M Watanabe K Fujiwara S Kurasawa T Wakabayashi T Tsuzuki M Iguchi K Yamori T 《Chemical & pharmaceutical bulletin》2003,51(6):724-727
Two norcarotenoids, 1 and 2, related to peridinin (3) were isolated from the cultured dinoflagellate of the genus Symbiodinium, a symbiont of the Okinawan soft coral Clavularia viridis, which contains in abundance antitumor marine prostanoids such as clavulones. The structures of 1 and 2 were elucidated on the basis of spectroscopic analysis. These compounds showed significant growth-inhibitory activity in vitro toward cancer cells. Analysis of fatty acids of the dinoflagellate was also carried out, suggesting that the marine prostanoids are produced by the host soft coral itself. 相似文献
887.
Kunishima M Yamamoto K Watanabe Y Hioki K Tani S 《Chemical communications (Cambridge, England)》2005,(21):2698-2700
A novel immobilized dehydrocondensing reagent comprised of a triazine-type dehydrocondensing reagent itself in a polymerized form was synthesized by copolymerization between tetra(ethylene glycol) bis(dichlorotriazinyl) ether and tris(2-aminoethyl)amine. 相似文献
888.
Kiyoshi Shibata Hiroshi Kimura Akira Tsuchida Tsuneo Okubo Shohei Sato Kohji Yoshinaga 《Colloid and polymer science》2006,284(4):372-379
Electro-optic responses of colloidal crystals consist of poly(maleic anhydride-co-styrene)-modified silica spheres (P(MA-ST)/SiO2) in acetonitrile and the crystals immobilized with a gelator, N-benzyloxycarbonyl-L-isoleucilaminooctadecane (Z-L-Ile-C-18), are studied by reflected-light intensity measurements and time-resolved reflection spectroscopy. Application of
an alternating electric field deforms P(MA-ST)/SiO2 crystal lattices reversibly. The response waveforms from the crystals are dependent on the frequency and strength of the
applied electric field; similar dependencies have been qualitatively observed for the colloidal crystals consisting of polystyrene
or silica spheres in aqueous media in our previous studies. Both gelated and ungelated P(MA-ST)/SiO2 crystals change the reflection intensity, however, the amplitude is larger for the latter. The small response for the gelated
P(MA-ST)/SiO2 crystals is attributed to the higher elastic modulus (G). The G value of the gelated P(MA-ST)/SiO2 crystals in acetonitrile is estimated from the change in the inter-sphere distance to be 8.0 Pa, which is about 2.3 and 2.4
times larger than that for ungelated P(MA-ST)/SiO2 crystals in acetonitrile and colloidal silica crystals in aqueous media, respectively. 相似文献
889.
8-Fluorocarbapenem derivatives having various C-3 side chains were synthesized to study for the structure-activity relationship of carbapenems by in vitro biological evaluation. The introduction of fluorine at C-8 of racemic PS-5 led to slight improvements of the antimicrobial activity and the stability to renal dehydropeptidase-I. When D-cysteine was additionally introduced to the C-3 position of (+/-)-8-fluorocarbapenem, the diastereomeric separation of the 8-fluorocarbapenems became feasible. As expected from penicillins and cephalosporins, (+)-8-fluoro-3-D-cysteinylcarbapenem (+)-7a was antimicrobially active, whereas (-)-7b was inactive. It is worth noting, however, that (+)-7a was significantly more sensitive to renal dehydropeptidase-I than (-)-7b. Irrespective of the presence of fluorine at C-8, basic S-side chains at C-3, such as the pyridyl and pyrrolidyl groups, significantly improved in antimicrobial activity and dehydropeptidase-I stability. The combination of 8-fluorination with C-3 basic side chains in 7c--g resulted in a marked improvement of antimicrobial activity and dehydropeptidase-I stability. 相似文献
890.
S. Arai T. Watanabe Y. Ishikawa T. Oyama O. Hayashi T. Ishii 《Chemical physics letters》1984,112(3):224-227
The infrared multiple-photon decomposition of mixtures of C2F6 and Br2 has been examined as functions of various experimental parameters. Carbon-13 was found to be enriched in the main product CF3Br; the maximum enrichment factor was 35. The combination of this process with the IRMPD of CF3Br provides a closed chemical cycle for efficient carbon isotope separation 相似文献