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41.
Paola Zimmermann Crocomo Takahito Kaihara Soki Kawaguchi. Dr. Patrycja Stachelek Prof. Dr. Satoshi Minakata Prof. Dr. Piotr de Silva Prof. Dr. Przemyslaw Data Prof. Dr. Youhei Takeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(53):13390-13398
Novel electron donor–acceptor–donor (D-A-D) compounds comprising dibenzo[a,j]phenazine as the central acceptor core and two 7-membered diarylamines (iminodibenzyl and iminostilbene) as the donors have been designed and synthesized. Investigation of their physicochemical properties revealed the impact of C2 insertion into well-known carbazole electron donors on the properties of previously reported twisted dibenzo[a,j]phenazine-core D-A-D triads. Slight structural modification caused a drastic change in conformational preference, allowing unique photophysical behavior of dual emission derived from room-temperature phosphorescence and triplet–triplet annihilation. Furthermore, electrochemical analysis suggested sigma-dimer formation and electrochemical polymerization on the electrode. Quantum chemical calculations also rationalized the experimental results. 相似文献
42.
Hiroshi Torii Keiji Fujimoto Haruma Kawaguchi 《Journal of polymer science. Part A, Polymer chemistry》1996,34(7):1237-1243
Four kinds of water-soluble, nonionic azo compounds were studied in terms of their decomposition rate and initiator efficiency in radical polymerization, and then used for emulsion polymerization. They had relatively low initiator efficiency from 0.09 to 0.46. It was attributed to the susceptibility to a cage effect, depending on their molecular size and hydrophobicity. Four azo compounds initiated emulsion polymerization but nonionic latex particles were not obtained unexpectedly. Methanol-containing medium results in the formation of a bimodal particle size distribution as well as a bimodal molecular weight distribution. © 1996 John Wiley & Sons, Inc. 相似文献
43.
T Seki T Kawaguchi K Sugibayashi K Juni Y Morimoto 《Chemical & pharmaceutical bulletin》1990,38(3):740-743
A membrane permeation-controlled transdermal delivery system (MC-TDS) of isosorbide dinitrate (ISDN), a model drug, was prepared from polyvinyl alcohol aqueous gel containing the drug, a membrane consisting of ethylene-vinyl acetate copolymer membrane and acrylic adhesive (EV-a). The permeability of ISDN through the EV-a membrane was 2.5 times higher than that through excised hairless rat skin. The ratio of plasma concentration of ISDN after application of MC-TDS on stripped (damaged) skin relative to intact skin was lower than that after application of Frandol tape-S, a marketed ISDN TDS, which suggests that the EV-a membrane might work as a control membrane for overall delivery rate of ISDN to the body. When MC-TDS stored at 30 degrees C for 13.5-48h was applied to the damaged skin, however, the initial plasma concentration of ISDN was very much higher than the expected therapeutic level and was not controlled by the EV-a membrane. The initial high plasma concentration of ISDN after application of the stored MC-TDS on the damaged skin was due to migration of ISDN from the reservoir to the adhesive during storage at 30 degrees C. The migration of drugs into the adhesive might be an important problem in developing efficient MC-TDS. 相似文献
44.
45.
The dynamic changes in ferroelectric liquid crystal (FLC) molecular alignments under an applied electric field are examined
by observing the formation of conoscopic figures with a time resolution of 0.1 ms. Close agreements between observed and simulated
conoscopic figures under low voltage (30 V) were obtained. Under high voltage (120 V), however, the observed conoscopic figures
became blurred between 0.8 ms and 1.1 ms after reversal of the electric field. The light scattering producing the blurriness
occurred due to the development of fast transient molecular alignments during the switching transition above the applied voltage
70 V. 相似文献
46.
Temperature dependent Mössbauer measurements are done on the samples of La1–x
Ca
x
Mn1–y
57Fe
y
O3 with x=0 and 0.25, and y=0.01. With decreasing temperature, the specimen with x=0.25 shows a paramagnetic to ferromagnetic transition around 175 K. In the specimen x=0.0, the temperature dependence of both the center shift () and the recoilless fraction (f) can be fitted very well with the Debye theory with a
D=320±50 K. But for the specimens with x=0.25, f and show distinct deviations from the Debye behavior in the temperature range in which the resistivity shows a sharp decrease. Dips observed in both the f and around the transition temperature suggest that the Jahn–Teller distortion observed in these systems is dynamic in nature. 相似文献
47.
Morita H Kawaguchi H Yoshimura T Tsukurimichi E Shimasaki C Horn E 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(21):3976-3983
5-(N-p)-Toluenesulfonyl)iminothianthrenes, whose sulfur atoms are oxidized to a sulfoxide or sulfone at the 10-position, were hydrolysed readily in high yield to N-unsubstituted-sulfilimines by using concentrated H2SO4. During hydrolysis, 10-monoxy-5-N-unsubstituted-sulfilimines were obtained as a separable mixture of the cis and trans isomers. The stereochemical interconversion of these compounds was studied under both hydrolytic and thermal conditions and their structures were elucidated by using X-ray crystallography. 相似文献
48.
Sakagami M Horie K Nakamoto K Kawaguchi T Hamana H 《Chemical & pharmaceutical bulletin》2000,48(9):1256-1263
Sialyl Lewis X (SLeX) is well known as a ligand of the cell adhesion molecule E-selectin which is specifically expressed at inflammatory lesion sites. We have synthesized several SLeX-polysaccharide conjugates and examined their potential for drug delivery to inflammatory lesions. The AUC (area under the blood concentration-time curve) 0-24 h of SLeX-CMCht (1), SLeX-CMPul (2) and SLeX-DSH (3) at the inflammatory lesion was about 60-, 300-, and 30-fold higher than that of the monovalent SLeX (7), respectively. Moreover, 1 showed 2-fold higher accumulation in the inflammatory lesion than SLN-CMCht (4), and 2 showed 2.5-fold higher accumulation than SLN-CMPul (5). 相似文献
49.
50.
T. Sato A. Narazaki Y. Kawaguchi H. Niino 《Applied Physics A: Materials Science & Processing》2004,79(4-6):1477-1479
Laser irradiation of solid nitrogen containing cyanuric triazide (C3N12) could generate highly reactive carbon nitride species, NCN and dicyanocarbodiimide. These species were generated in the solid nitrogen at 20 K. After laser photolysis, generated reactive species were concentrated by removal of nitrogen, and converted into a film-like product. Thus, the obtained product was characterized by means of FTIR, SEM, and XPS measurements. The product was assigned to amorphous carbon nitride with relatively high nitrogen content (N/C=0.91.3). PACS 81.15.Fg; 82.33.-z; 68.55.Nq 相似文献