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991.
Let be a distance-regular graph of diameterd, valencyk andr=max{i|(c
i
,b
i
)=(c
1,b
1)}. In this paper, we prove that
相似文献
992.
Ryosuke Kadono Akira Matsushita Kusuo Nishiyama Kanetada Nagamine 《Hyperfine Interactions》1994,87(1):979-984
In order to shed new light on the initial loss of muon spin polarization, or socalled missing fraction, which is commonly observed in non-metallic solids, we have studied muon-induced excitation in various alkali halides by measuring the luminescences associated with the radiative decay of the self-trapped excitons (STE). The result strongly suggests that the spin-exchange interaction between muonium and muon radiolysis products including STE's causes fast muon depolarization in those materials. 相似文献
993.
Jiro Motoyoshiya Akira Takagi Kiyoichi Hirakawa Toshio Kakurai 《Journal of heterocyclic chemistry》1986,23(2):597-599
Several ketenimines bearing ester groups were prepared and their thermal reactions gave 2-alkoxy-3-substituted-4-quinolinols VIa-e via presumed iminoketene intermediates. Subsequent oxidation of 2-alkoxy-3-(3-methylbut-2-enyl)-4-quinolinols VIc and VId provided pyranoquinolines VIIIa and VIIIb. 相似文献
994.
Jyunichi Koyanagi Katsumi Yamamoto Kouji Nakayama Akira Tanaka 《Journal of heterocyclic chemistry》1994,31(4):1093-1095
4-endo-5-exo-Dibromo-3-methyl-3,6-endo-oxyperhydrophthalic anhydride 3b and 4-exo-5-endo-dibro-mo-3-methyl-3,6-endo-oxyperhydrophtbalic anhydride 3c were isolated from the bromo-adducts of 3-methyl-3,6-endo-oxy-1,2,3,6-tetrahydrophthalic anhydride 2. When 3b or 3c was heated in quinoline, only 3-bromo-2-methylfuran 4 was obtained from 3b and only 4-bromo-2-methylfuran 5 from 3c. 相似文献
995.
The reaction of phenyl or 1-alkenyl iodides with 1-alkenyl-1,3,2-benzodioxaboroles readily obtainable via the hydroboration of 1-alkynes, gives the corresponding “head-to-tail” cross-coupling products, 2-phenyl-1-alkenes or 2-alkyl-1,3-alkadienes, in good yields. The reaction is effectively catalyzed by catalytic amounts of palladium compounds in the presence of triethylamine. 相似文献
996.
Shigeru Kubota Toshimoto Moriwaki Torahiko Ando Akira Fukami 《Journal of polymer science. Part A, Polymer chemistry》1987,25(8):2241-2250
Polyquinazolones containing m-substituted phenyl groups (Br, Cl, F, CH3O, NO2, and CH3) on the quinazolone ring were synthesized in m-cresol, and their thermal properties were studied by using dynamic thermogravimetry and isothermal weight loss. Polyquinazolones with intrinsic viscosities in the range 0.2–1.6 dL/g were synthesized. The introduction of substituted groups into the pendant phenyl group resulted in a decrease in the glass transition temperature and the thermal stability. Oxidative thermal stability of the polyquinazolones was dependent on the position of substituted groups on the pendant phenyl group. The introduction of substituted groups into the meta position reduced thermal stability more than did the introduction into the para position. 相似文献
997.
Choji Kashima Akira Katoh Yuko Yokota Yoshimari Omote 《Journal of heterocyclic chemistry》1981,18(7):1469-1470
1,4,6-Trisubstituted 3,6-dihydro-2-(1H)pyrimidinones (Ia-d) easily underwent the ring opening reaction with hydroxylamine hydrochloride to afford the oximes (IIa-d) in good yields. In the case of 3,6-dihydro-6-methyl-I-phenyl-2-(1H)pyrimidinone (Ie), 2-anilinobutyronitrile (III) was obtained in addition to the oxime (IIe). Dihydro-2-(1H)pyrimidinone (IV) and -thiones (V and VI) did not undergo the ring opening reaction. 相似文献
998.
Xin -Tong Zhang Taketo Taguchi Hai -Bin Wang Qing -Bo Meng Osamu Sato Akira Fujishima 《Research on Chemical Intermediates》2007,33(1-2):5-11
The stability of the TiO2/ruthenium dye/CuI solid-state solar cell was investigated under continuous simulated sunlight illumination. The cells showed fast degradation under full-spectrum sunlight illumination, but showed rather good stability when the ultraviolet part of the illumination was removed. XPS measurements showed evidence that TiO2 could oxidize CuI in the presence of UV light. The photo-degradation mechanism of the cells is thus discussed on the basis of the photo-oxidative function of TiO2. The long-term stability of the solid-state dye-sensitized solar cell (DSSC) was found to be improved under simulated sunlight by coating the TiO2 porous electrode with an ultra-thin MgO layer, which was able to block the photo-oxidative activity of the TiO2. 相似文献
999.
Masafumi Hirano Kohtaro Osakada Hiroyuki Nohira Akira Miyashita 《The Journal of organic chemistry》2002,67(2):533-540
Full elucidation for stable, colorless, and meta-stable colored structures of a new spirobenzothiopyran has been achieved both in the solid state and in a solution. 1',3',3'-Trimethyl-6-nitrospiro[(2H)-1-benzothiopyran-2,2'-indoline] with an ester group as a substituent at the 8-position of 1-sp shows photochromism. The blue-green colored species resulted from UV irradiation (365 nm) in one minute and spontaneously bleaches within one minute in acetone and methanol at 27 degrees C. UV exposure (365 nm) of 1-sp in methanol for 3 h at room temperature results in the growth of deep blue needlelike single crystals of the open form of spirobenzothiopyran, photomerocyanine 1-pmc, whose structures in the solid state and in solution were obtained unambiguously. The X-ray structural analysis of 1-pmc revealed the molecular structure of the zwitterionic photomerocyanine with s-trans,s-trans conformation. 1-pmc is soluble to polar solvents and thermally returns to 1-sp. In the DMSO solution, 1-pmc is found to return slowly to 1-sp (1-pmc gave only 18% of 1-sp for 30 min at 22 degrees C). The detailed NMR studies in DMSO-d(6) including COSY and NOE techniques as well as isotope labeling of the compound showed the structure with s-trans,s-cis conformation in a solution. 相似文献
1000.
Masahiro Tsunooka Kohei Kotera Makoto Tanaka 《Journal of polymer science. Part A, Polymer chemistry》1977,15(1):107-117
Copolymers bearing pendant O-acyloxime groups were synthesized by two methods: copolymerizations of oxime acrylate (methyl β-naphthyl ketone oxime acrylate or benzophenone oxime acrylate) and styrene, condensation of acrylic acid—styrene copolymer with oximes (benzophenone oxime, p-nitrobenzophenone oxime, methyl β-naphthyl ketone oxime, benzalacetone oxime or 9-fluorenone oxime). The photochemical behavior of the O-acyloxime copolymers changed markedly with the irradiation conditions: irradiation of benzene solutions led to degradation in air and crosslinking under nitrogen, while irradiation of solid films in air resulted in simultaneous degradation and crosslinking. Photolysis of methyl β-naphthyl ketone oxime acetate, a model for the O-acyloxime copolymer, in benzene solution under nitrogen resulted in scission of the N? O bond. The same reaction was observed in the irradiation of the O-acyloxime copolymers. It is suggested that formation of free radicals on the polymer chains via scission of the N? O bond is followed by decarboxylation. In the absence of oxygen, crosslinking of the polymer by recombination of the free radicals competes with degradation via β-scission. In the presence of oxygen, autoxidative degradation predominates. 相似文献