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281.
The neutral square-planar complexes [Pt(RNH2)2(NHCO(t)Bu)2] (R = H, 1; Et, 2) and [Pt(DACH)(NHCO(t)Bu)2] (DACH = 1,2-diaminocyclohexane, 3) act as metalloligands and make bonds to closed-shell Tl(I) ions to afford one- and two-dimensional platinum-thallium oligomers or polymers based on heterobimetallic backbones. A series of heteronuclear platinum(II)-thallium(I) complexes have been synthesized and structurally characterized. The structures of the Pt-Tl compounds resulted from [Pt(RNH2)2(NHCO(t)Bu)2] and TlX [X = NO3(-), ClO4(-), PF6(-), and Cp2Fe(CO2)2(2-)] are dependent on both counteranions and the amine substituents. The compounds [Pt(NH3)2(NHCO(t)Bu)2Tl]X (X = NO3(-), 8; ClO4(-), 9) adopt one-dimensional zigzag chain structures consisting of repeatedly stacked [Pt(NH3)2(NHCO(t)Bu)2Tl]+ units, whereas [{Pt(NH3)2(NHCO(t)Bu)2}2Tl2]X2 (X = PF6(-), 10) consists of a helical chain. Compound 3 reacts with Tl+ to give [{Pt(DACH)(NHCO(t)Bu)2}2Tl](NO3) x [Pt(DACH)(NHCO(t)Bu)2] x 3 H2O (14) and one-dimensional polymeric [{Pt(DACH)(NHCO(t)Bu)2}2Tl2]X2 (X = ClO4(-), 15; PF6(-), 16). Reactions of [Pt(DACH)(NHCOCH3)2] with Tl+ ions afford one-dimensional coordination polymers [{Pt(DACH)(NHCOCH3)2}2Tl2]X2 (X = NO3(-), 17; ClO4(-), 18; PF6(-), 19). The polymeric [{Pt(DACH)(NHCOR')2}2Tl2]2+ (R = CH3, (t)Bu) complexes adopt helical structures, which are generated around the crystallographic 2(1) screw axis. The distance between the coils corresponds to the unit cell length, which ranges from 22.58 to 22.68 A. The platinum-thallium bond distances fall in a narrow range around 3.0 A. The complexes derived from [Pt(NH3)2(NHCO(t)Bu)2] are luminescent at 77 K. The trinuclear complexes [{Pt(RNH2)(NHCO(t)Bu)2}2Tl]+ do not emit at room temperature but are emissive at 77 K, whereas the polymeric platinum-thallium complexes containing 1,2-diaminocyclohexane are intensively luminescent at both room temperature and 77 K. The color variations are interesting; 15 exhibits intense yellow-green, 16 exhibits green, and 17-19 exhibit blue luminescence. The presence of bonding between platinum and thallium is supported by the short metal-metal separations and the strong low-energy luminescence of these compounds in their solid states. 相似文献
282.
Tamami Koshiyama Masako Kato 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(4):m173-m176
The title dinuclear platinum(III) complex, [Pt2(C11H8N)2(C5H4NS)4], forms two crystal structures, viz. the non‐solvated and acetonitrile‐solvated (C2H3N) forms. For both forms, two (2‐pyridylphenyl)platinum units are bridged by two pyridine‐2‐thiolate (pyt) anions in a head‐to‐tail configuration, and the other two pyridine‐2‐thiolate anions occupy the axial position, coordinated through their S atoms. The most remarkable difference between the two forms is the orientation of the axial monodentate ligands. Those for the solvated form are located over the 2‐pyridylphenyl ligands, being related by a twofold axis which lies through the centre of the Pt—Pt bond, while the axial pyt ligands for the non‐solvated form are oriented irregularly, which is attributable to the dimeric arrangement in the crystal. 相似文献
283.
Tanaka H Kanoh H Yudasaka M Iijima S Kaneko K 《Journal of the American Chemical Society》2005,127(20):7511-7516
H(2) and D(2) adsorption on single-wall carbon nanohorns (SWNHs) have been measured at 77 K, and the experimental data were compared with grand canonical Monte Carlo simulations for adsorption of these hydrogen isotopes on a model SWNH. Quantum effects were included in the simulations through the Feynman-Hibbs effective potential. The simulation predictions show good agreement with the experimental results and suggest that the hydrogen isotope adsorption at 77 K can be successfully explained with the use of the effective potential. According to the simulations, the hydrogen isotopes are preferentially adsorbed in the cone part of the SWNH with a strong potential field, and quantum effects cause the density of adsorbed H(2) inside the SWNH to be 8-26% smaller than that of D(2). The difference between H(2) and D(2) adsorption increases as pressure decreases because the quantum spreading of H(2), which is wider than that of D(2), is fairly effective at the narrow conical part of the SWNH model. These facts indicate that quantum effects on hydrogen adsorption depend on pore structures and are very important even at 77 K. 相似文献
284.
The intramolecular ruthenium(II)-catalyzed radical addition of the trichloroacetyl pendant group to the 2-oxazolone skeleton is greatly enhanced in the presence of catalytic Lewis acids including rare earth metal triflates, thus providing a convenient route to a highly potential chiral synthon for vic-amino alcohols. 相似文献
285.
286.
Takahisa Anada Masako Ogawa Hisashi Yokomizo Yoshihisa Ozaki Tohru Takarada Yoshiki Katayama Mizuo Maeda 《Analytical sciences》2003,19(1):73-77
We describe here a method of affinity capillary electrophoresis in which oligodeoxynucleotide (ODN) was immobilized onto the inner surface of the capillary. The immobilized ODN functioned successfully as an affinity ligand for sequence-based DNA separation. Six- or 12-mer ODN with a sequence complementary to one of the c-K-ras gene was used as an immobilized ligand. When the 12-mer ODN was used, the detection peak for the complementary ODN disappeared selectively, while the single-base mutant was detected as usual. In contrast, when the 6-mer ODN was used as the affinity ligand with a mixture of the complementary ODN and its single-base mutant, it was possible to detect both as completely separate peaks. That is, the separation mode was dependent on the base number of the immobilized ODN used as an affinity ligand. 相似文献
287.
288.
289.
Sans résumé
Work supported by the National Science Foundation under NSF-GP780. 相似文献
Work supported by the National Science Foundation under NSF-GP780. 相似文献
290.
Koso Aoki Yuji Kawanishi Takahiro Seki Masako Sakuragi Takashi Tamaki Kunihiro Ichimura 《Liquid crystals》1995,19(1):119-125
In connection with the mechanism of reversible alignment change of nematic liquid crystals induced by photoisomerizable azobenzene molecules attached to a quartz surface, a static contact angle measurement was carried out for azo-modified plates before and after UV irradiation. The results were not in line with the so-called Friedel-Creagh-Kmetz rule which claims that the alignment is governed by a mutual relationship between a substrate surface energy and surface tension of a liquid crystal. On the other hand, electronic absorption spectra of the plate demonstrated that the ratio of an absorbance at around 340 nm to that at around 240 nm of the azo-chromophore on the surface is reduced by wetting the surface with a UV-transparent nematic liquid crystal. This reflects that the surface azobenzene units are induced to stand approximately perpendicular to the surface upon contact with the liquid crystal. Further discussion is made concerning the photo-induced homogeneous alignment triggered by a rubbed and azo-modified quartz plate determined by polarized absorption spectroscopy. 相似文献