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31.
32.
Akane Suzuki Daisuke Nagai Bungo Ochiai Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2004,42(23):5983-5989
The trifunctional five‐membered cyclic carbonate 2 and dithiocarbonate 3 were successfully synthesized by the reaction of trifunctional epoxide 1 with carbon dioxide and carbon disulfide, respectively. The crosslinking reactions of 2 with p‐xylylenediamine or hexamethylenediamine were carried out in dimethyl sulfoxide at 100 °C for 48 h to produce the corresponding crosslinked poly(hydroxyurethane)s quantitatively. The crosslinking reactions of 3 with both p‐xylylenediamine and hexamethylenediamine, followed by acetylation of thiol moiety, produced the corresponding crosslinked poly(thioester–thiourethane)s quantitatively. The obtained crosslinked poly(hydroxyurethane)s were thermally more stable than the analogous crosslinked poly(thioester–thiourethane)s, probably because of less thermal stability of thiourethane moiety than hydroxyurethane moiety. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5983–5989, 2004 相似文献
33.
Bungo Ochiai Jun‐ichi Nakayama Masayuki Mashiko Yoshiro Kaneko Tomomi Nagasawa Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2005,43(23):5899-5905
This article describes the polyaddition of bifunctional five‐membered cyclic carbonates and diethylenetriamine. The polyaddition proceeded via the selective addition of the primary amino group to the cyclic carbonates to give poly(hydroxyurethane)s bearing a secondary amine structure in the main chain. The resulting poly (hydroxyurethane) having a secondary amine structure was crosslinked by a reaction with a bifunctional dithiocarbonate to give a networked poly(hydroxyurethane–mercaptothiourethane). © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5899–5905, 2005 相似文献
34.
Yoshifumi Hanada Teizi Tanizaki Minoru Koga Hiroaki Shiraishi Mitsuyuki Soma 《Analytical sciences》2002,18(4):445-448
Liquid chromatography/mass spectrometry (LC/MS) has been applied to the analysis of triphenylboron, which has been produced as a substitute for organotin compounds, in water. Although commercial triphenylboron compounds are produced as pyridinyl complexes, the chemical form in water is supposed to be mainly triphenylboron after liberating pyridine. The triphenylborons were extracted from water with an Empore C18 extraction disk under acidic condition, and the extracts were introduced directly into a liquid chromatograph-mass spectrometer equipped with a negative ion electrospray ionization interface. Identification of the compounds was performed with specific ions produced from the triphenylboron, and a quantitative analysis was carried out using the peak areas. The average recoveries from distilled water, seawater and river water at 0.30 ng/ml were 92.3, 100 and 85.3%, respectively. A detection limit of 0.023 ng/ml for triphenylboron was achieved. 相似文献
35.
Hiroshi Ochiai Heisaburo Shindo Hitoshi Yamamura 《Journal of Polymer Science.Polymer Physics》1971,9(3):431-435
The effects of stereoregularity on the low-temperature relaxation processes were studied by dynamic mechanical measurements on isotactic and syndiotactic polyisobutyl methacrylates (iso-PiBMA and syn-PiBMA). The α, β, and γ relaxation processes were observed in both stereoregular forms. Both the α, and β loss peaks were at lower temperatures for iso-PiBMA than for syn-PiBMA. The γ loss peak was observed at about ?155°C at 30 Hz for both forms, and the apparent activation energy of this process was same for both samples within experimental error (6.7 ± 0.5 kcal/mole). It was reduced from these results that the α and β processes are both considerably influenced by the isotactic configuration but the γ process is not. 相似文献
36.
K. Ishibashi Y. Aoyagi S. Namba Y. Ochiai M. Kawabe K. Gamo 《Superlattices and Microstructures》1991,9(4)
Magnetoresistance measurements have been performed in narrow GaAs/AlGaAs wires in order to study the scattering process in mesoscopic wires. Amplitude analysis of the Shubnikov -de Haas oscillations shows that electrons have two scattering times, depending upon the magnetic field range. The critical field which separates these scattering times seems to be determined by the relation between the wire width and the electron cyclotron radius. This effect is discussed in terms of the electron trajectories in a wire under the magnetic field. 相似文献
37.
38.
Masahito Ochiai Munetaka Kunishima Kenzo Sumi Yoshimitsu Nagao Eiichi Fujita Masao Arimoto Hideo Yamaguchi 《Tetrahedron letters》1985,26(37):4501-4504
New general methods for the synthesis of alkynyl(phenyl)iodonium tetrafluoroborate 2 from alkynyltrimethylsilanes 1 utilizing the combination of iodosylbenzene and triethyloxonium tetrafluoroborate or boron trifluoride etherate were developed. The medium effect observed in the reaction was also discussed. 相似文献
39.
40.
Ochiai M Nishi Y Mori T Tada N Suefuji T Frohn HJ 《Journal of the American Chemical Society》2005,127(30):10460-10461
Reported here for the first time are the synthesis, isolation, and characterization of hypervalent beta-haloalkenyl-lambda3-bromanes. Exposure of terminal alkynes to p-trifluoromethylphenyl(difluoro)-lambda3-bromane activated by BF3-i-Pr2O resulted in fluoro-lambda3-bromanation of the triple bonds in a Markovnikov fashion, yielding (E)-beta-fluoroalkenyl-lambda3-bromanes stereoselectively in good yields. 5-Chloro-1-pentynes undergo domino lambda3-bromanation-chlorine shift-fluorination or lambda3-bromanation-chlorine shift-alkyl shift-fluorination reaction, depending on the substituents and afford (E)-beta-chloroalkenyl-lambda3-bromanes stereoselectively in high yields. The beta-chloroalkenyl-lambda3-bromanes contain three kinds of halogen atoms, F, Cl, and Br, in the molecule. 相似文献