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91.
Ken Taguchi Akihiko Toda Yoshihisa Miyamoto 《Journal of Macromolecular Science: Physics》2013,52(6):1149-1157
Crystallization of isotactic polystyrene (it‐PS) from dilute solution at high supercooling has been investigated by dynamic light scattering (DLS). We successfully obtained simultaneously, in situ in solutions, the time developments of both random coils of it‐PS molecules and the growing crystals. The size of coils remains constant during growth, while the crystals pass through two stages, that is, an induction period at the early stage with very slow growth rates and a subsequent linear growth stage. It is confirmed that the temperature dependence of the linear growth rates, determined by DLS, agree well with that determined by electron microscopy. The temperature dependences of the growth rate and the inverse of induction time are dependent on the viscosity of solvent, which indicates that all dynamics are dominated by the segmental motion of polymer chains in solution at high supercoolings (low temperatures). Two possibilities are proposed for the induction period. 相似文献
92.
We estimated internal CO2 conductance (gi ) for C3 plant species of different life forms (annual herbs, deciduous trees and evergreen trees) grown in a variety of environments to examine the effect of g i on their leaf carbon isotope ratio (i13C). The purpose of this study was to test the validity of using i13C as an index of photosynthetic water use efficiency (WUE). When comparing deciduous tree species grown in contrasting light environments, there was a strong positive relationship between i13C and WUE. Similarly, i13C was positively correlated to WUE when comparing the different species of evergreen trees. However, the difference in WUE between evergreen and deciduous tree species did not relate to that in leaf i13C. In addition, WUE was similar between highland and lowland herbaceous plants, although the former had a much higher i13C. The positive relationship between i13C and WUE did not hold across different life forms and different altitudes when differences in gi did not relate to those in stomatal conductance, resulting in independence of chloroplast CO2 partial pressure from intercellular CO2 partial pressure. 相似文献
93.
Effects of pressure and temperature on the solubility of monosodium L-glutamate monohydrate in water
Yoshihisa Suzuki Hiroshi Matsuo Yoshikata Koga Katsuya Mukae Tetsuya Kawakita Seiji Sawamura 《高压研究》2013,33(2):93-104
Abstract The solubility of monosodium L-glutamate monohydrate (MSG.H2O) in water was measured at pressures in the range of 0.10-300MPa and 298.15K. The density of MSG solution at high concentrations and heat of solution at saturated concentration were also measured at atmospheric pressure. The solubility, ms, increased with increasing pressure and the pressure coefficient, Θp, [?(? In ms,? p)T] at 0.10 MPa was (2.0 ± 0.1) × 10-10Pa-1. It agrees well with (2.1 ±0.2)× 10-10 Pa-1 thermodynamically estimated using the partial molar volume, the activity coefficient of the solute in solution, and the molar volume of the crystal. The excellent agreement at 0.10MPa gives us confidence in the solubility data at higher pressures. The heat of solution data and other pertinent values were used to calculate the temperature coefficient of solubility, ΘT [? (? In ms/?(1/T))p], by a thermodynamic equality. The resulting ΘT compares well with the data directly measured by Ogawa. 相似文献
94.
Optical trapping and guiding using laser have been proven to be useful for non-contact and non-invasive manipulation of small objects such as biological cells, organelles within cells, and dielectric particles. We have numerically investigated so far the motion of a Brownian particle suspended in still water under the illumination of a speckle pattern generated by the interference of coherent light scattered by a rough object. In the present study, we investigate numerically the motion of a particle in a water flow under the illumination of a speckle pattern that is at rest or in motion. Trajectory of the particle is simulated in relation with its size, flow velocity, maximum irradiance, and moving velocity of the speckle pattern to confirm the feasibility of the present method for performing optical trapping and guiding of the particle in the flow. 相似文献
95.
Alkylation‐, Heating‐, and Doping‐Induced Emission Enhancement of a Polyaromatic Tube in the Solid State 下载免费PDF全文
Kiyonori Kuroda Masafumi Otsuki Dr. Kohei Yazaki Dr. Yoshihisa Sei Prof. Dr. Munetaka Akita Dr. Michito Yoshizawa 《化学:亚洲杂志》2018,13(5):515-519
A polyaromatic tube with a subnanometer‐sized cavity was efficiently prepared on a gram‐scale through the stereo‐controlled cyclotrimerization of a diphenylanthracene derivative as a key step. The facile exterior alkylation of the polyaromatic framework leads to a moderately fluorescent tube (R=‐OC10H21; ΦF=20 %) in the solid state. The emission intensity of the solid‐state alkyl‐substituted tube is remarkably enhanced upon heating (up to 1.6 times, ΦF=31 %) as well as doping with fluorescent dyes (up to 4.2 times, ΦF=83 %) through efficient energy transfer. 相似文献
96.
Frontispiece: Entropy‐Driven Diastereoselectivity Improvement in the Paternò–Büchi Reaction of 1‐Naphthyl Aryl Ethenes with a Chiral Cyanobenzoate through Remote Alkylation 下载免费PDF全文
97.
Yoshihisa Okamoto Yoshimi Yamaguchi Mitsuaki Maeda Yoshihisa Kurasawa 《Journal of heterocyclic chemistry》2008,45(3):717-721
Fused tetracycles, 6‐alkyl‐3‐alkoxy‐2‐cyano‐4,5,6a,11‐tetraazabenzo[a]fluorene derivatives ( 5a , b , c , d , e , f ), are synthesized from 2‐alkoxy‐5‐(benzimidazol‐2‐ylidene)‐3‐cyano‐6‐imino‐5,6‐dihydro‐pyridines ( 4b , c ), and when refluxed in ethyl orthoacetate or ethyl orthopropionate, the elecrophilic aromatic substitution occurs at the ortho position of the cyanopyridine ring in the fused tetracycles ( 5b , c , e , f ) to afford 6‐alkyl‐3‐alkoxy‐2‐cyano‐1‐ethyl‐4,5,6a,11‐tetraazabenzo[a]fluorenes( 6b , c , e , f ). 相似文献
98.
2-Nitrophenyl isocyanide is introduced as a convertible isocyanide with demonstration of its feasibility and applicability in an efficient synthesis of the fused gamma-lactam beta-lactone bicycle of proteasome inhibitor omuralide. Starting from a linear keto acid precursor, the fused gamma-lactam beta-lactone bicycle was prepared in four steps by a sequential biscyclization strategy; a stereocontrolled Ugi reaction and the concomitant direct beta-lactonization following the formation of an N-acylbenzotriazole intermediate. The N-acylbenzotriazole is amenable to intra- or intermolecular attack from a variety of nucleophiles with a catalytic amount of base to form the pyroglutamic acid derivatives. 相似文献
99.
The racemic synthesis of the common propellane core structure found in various hasubanan alkaloids is reported. The successful completion hinged upon the stereocontrolled construction of the cis-substituted heterobicycle as a precursor for the intramolecular Dieckmann condensation. A novel strategy is introduced for the facile hydrolysis of a sterically demanding carboxamide under a mild condition. The 2-nitroanilide obtained by the Goldberg arylation of a carboxamide with 2-iodonitrobenzene was readily converted to the corresponding ester derivative by way of N-acylbenzotriazole. We expect that the reported synthetic route will allow the synthesis of a series of hasubanan alkaloids starting from the correspondingly functionalized 2-tetralone derivatives. 相似文献
100.
Lu R Yang C Cao Y Tong L Jiao W Wada T Wang Z Mori T Inoue Y 《The Journal of organic chemistry》2008,73(19):7695-7701
A series of 6-O-benzoyl-beta-cyclodextrins (CDs) with methyl, methoxy, methoxycarbonyl, and bromo substituent(s) at the ortho-, meta-, and/or para-position(s) were synthesized as chiral sensitizing hosts for the use in supramolecular enantiodifferentiating photoisomerization of (Z)-cyclooctene (1Z) to its chiral (E)-isomer (1E). The complex stability constants (K(S)) of the modified beta-CDs with 1Z in aqueous methanol solutions were highly sensitive to the substituent(s) introduced to the benzoate moiety, and the log K(S) values decreased linearly with slightly different slopes with increasing methanol content. The enantiomeric excess (ee) of 1E obtained upon photosensitization with these hosts was a critical function of the size and position of the substituent, varying from almost zero to 46% ee. This indicates that even an apparently small structural difference between methyl and methoxy can critically affect the enantiodifferentiating photoisomerization of a guest included in the chiral cavity, probably through manipulation of both the orientation of ground-state 1Z and the subsequent rotational relaxation of excited 1Z inside the chiral cavity. 相似文献