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61.
Two new tetranor-cycloartane glycosides (1, 2) were isolated from Cimicifuga Rhizome. Their structures were determined by spectroscopic analysis. These compounds suggested the existence of a biogenetic pathway into C-23 lactone-type cycloartane glycosides. 相似文献
62.
Kimura M Sakaguchi A Ohta K Hanabusa K Shirai H Kobayashi N 《Inorganic chemistry》2003,42(9):2821-2823
A new class of sterically hindered phthalocyanine has been synthesized and characterized. Pentaphenylbenzene units were introduced at the periphery of each phthalocyanine to yield a sterically protected metal center. The attachment of the bulky oligophenylbenzene units resulted in the complete isolation of individual MPc molecules. The pockets around a cobalt center affect selectivity in the ligation of pyridines that have different sizes and shapes. 相似文献
63.
Hidayah Ariffin Haruo Nishida Yoshihito Shirai Mohd Ali Hassan 《Polymer Degradation and Stability》2008,93(8):1433-1439
The thermal degradation of poly(3-hydroxybutyrate) (PHB) was investigated by kinetic analyses in detail to clarify its complex degradation behavior, resulting in a finding of mixed mechanisms comprising at least a thermal random degradation with subsequent auto-accelerated transesterification, and a kinetically favored chain reaction from crotonate chain ends. The thermal degradation behavior of PHB varied with changes in time and/or temperature. From the kinetic analysis of changes in molecular weight, it was found that a non-auto-catalytic random degradation proceeding in the initial period was followed by an auto-accelerated reaction in the middle period. From the kinetic analysis of weight loss behavior, it is proposed that there are some kinetically favored scissions occurring at the chain ends, where the degradation proceeded by a 0th-order weight loss process in the middle stage. The observed 0th-order weight loss process was assumed to be an unzipping reaction occurring at ester groups neighboring the crotonate end groups. 相似文献
64.
57Fe Mössbauer and FT-IR of 60CaO·(40-x)Ga2O3·xFe2O3 glasses revealed that Fe(III)O4 tetrahedra occupy substitutional sites of Ga(III)O4 tetrahedra. The activation energy for crystallizaation (E
a) obtained from DTA study decreases distinctly from 8.9 to 4.8 eV with an increase in the Fe2O3 content. In the case of 40CaO·(60-x)Ga2O3·xFe2O3 glasses, a week doublet due to Fe(II)O4 tetrahedra or Fe(III)O6 octahedra was observed in addition to Fe(III)O4 tetrahedra. The E
avalue decreases gradually from 7.1 to 5.6 eV with an increasing Fe2O3 content. These results indicate that a large amount of Fe2O3 in the network structure is favorable for the crystallization of calcium gallate glass, since it reduces the chemical bond strength. 相似文献
65.
Kamada H Asobe M Honjo T Takesue H Tokura Y Nishida Y Tadanaga O Miyazawa H 《Optics letters》2008,33(7):639-641
We demonstrate 1500 nm band single-photon detection with low dark-count noise and a potentially high efficiency, which may allow long distance and high-bit-rate quantum key distribution. By developing frequency upconversion devices based on periodically poled lithium niobate waveguides, which are specifically designed to use a pump wavelength longer than that of communication-band photons, we completely eliminate the dark-count noise caused by parasitic nonlinear processes in the waveguide. We observed an internal conversion efficiency as high as 40% and demonstrated scaling down to the single photon level while maintaining a background dark-count rate of 10(2)s(-1). 相似文献
66.
Two new cycloartane glycosides, named aquilegiosides K and L, have been isolated from the dried underground parts of Aquilegia vulgaris. Their structures were determined by two dimensional (2D) NMR spectroscopic analysis and chemical evidence. 相似文献
67.
Eiichi Masumoto Hiroshi Maruoka Fumi Okabe Sho Nishida Ryoko Tomita Toshihiro Fujioka Kenji Yamagata 《Journal of heterocyclic chemistry》2012,49(4):893-899
A novel synthetic route to 4‐pyridazineacetic acids 10 – 12 has been achieved by the ring‐expansion reaction of N‐cyanomethylated 3‐pyrazoline‐4‐acetic acids 7 – 9 . 1H‐Pyrazole‐4‐acetic acids 1 – 3 were reacted with iodoacetonitrile in the presence of triethylamine in refluxing acetonitrile to give the corresponding C‐cyanomethylated 1H‐pyrazole‐4‐acetic acids 4 – 6 as major products together with N‐cyanomethylated 3‐pyrazoline‐4‐acetic acids 7 and 8 as minor products. On the other hand, reactions of 1 and 3 with chloroacetonitrile in the presence of triethylamine in refluxing chloroform afforded the corresponding N‐cyanomethylated 3‐pyrazoline‐4‐acetic acids 7 and 9 as major products. Thermal treatment of 7 – 9 with sodium hydride in N,N‐dimethylformamide caused ring expansion to yield the corresponding 4‐pyridazineacetic acids 10 – 12 . 相似文献
68.
Unsaturated nitriles have been synthesized from trisubstituted olefins via ene-type chlorination and regioselective substitution with cyanide ion followed by double bond migration. 相似文献
69.
Morita Y Nishida S Kobayashi T Fukui K Sato K Shiomi D Takui T Nakasuji K 《Organic letters》2004,6(9):1397-1400
[structure: see text] A bowl-shaped neutral radical with a corannulene system has been designed and synthesized for the first time as a stable solid in air. An unequivocal characterization of the electronic properties of the radical shows that an appreciable amount of spin delocalization extends onto the corannulene unit's curved surface. 相似文献
70.
A simple method for the diastereoselective synthesis of racemic 1,2-diol mediated by low-valence niobium generated in situ is described. A 1,4-dioxane-toluene solvent system was found to be essential to achieve higher selectivities and to prevent other reactions of pinacols, such as deoxygenation and acetal formation. Aromatic aldehydes and ketones were converted to the corresponding pinacols with up to 97 and 85% de, respectively. 相似文献