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排序方式: 共有183条查询结果,搜索用时 15 毫秒
1.
Statistical Inference with Fractional Brownian Motion 总被引:3,自引:1,他引:2
Kukush Alexander Mishura Yulia Valkeila Esko 《Statistical Inference for Stochastic Processes》2005,8(1):71-93
We give a test between two complex hypothesis; namely we test whether a fractional Brownian motion (fBm) has a linear trend against a certain non-linear trend. We study some related questions, like goodness-of-fit test and volatility estimation in these models. 相似文献
2.
A commercial baker’s yeast was subjected to selection in a continuous turbidostat cultivation with increasing concentration of acetic acid. The final acetic acid content in fresh medium was 0.6% or 0.8% v/v. Two of seven selected variants were stable over 15 sequential shake flask cultivations without selection pressure. After laboratory scale production of baker’s yeast, one of the variants also showed increased acetic acid tolerance in sour dough. The overall raising power (mL CO2/h) in sour dough was improved 36%. 相似文献
3.
Mats J. Sundell Esko O. Pajunen Osmo O. E. Hormi Jan H. Nsman 《Journal of polymer science. Part A, Polymer chemistry》1993,31(9):2305-2311
The synthesis of some divinyl monomers—bis(vinylphenyl)ethane ( 2 ), bis(vinylbenzyloxy)hexane ( 3a ), and bis(vinylbenzyloxy)dodecane ( 3b ) is reported. Copolymers of the new monomers and styrene were evaluated as an alternative to divinylbenzene-crosslinked polymers for use as matrices and absorbents. The mechanical properties and the amount of residual double bonds in the copolymers were compared. It was found that the new copolymers, unlike the divinylbenzene-crosslinked polymers, retained their mechanical strength even at high crosslinking degrees. Stress at break values of 79, 68, and 18 N/mm2 were found for the polymers crosslinked with 20 mol % of 3a, 2 , and divinylbenzene; 5, 25 and 45% of the divinyl units in these polymers were left as pendant double bonds. Porous styrene– 2 copolymers were synthesized and shown to have lower surface areas than the corresponding divinylbenzene-crosslinked polymers. The pore size distribution showed that this was due to the absence of the smallest pores which are found in the divinylbenzene-crosslinked polymers in between heavily crosslinked nodules. © 1993 John Wiley & Sons, Inc. 相似文献
4.
Marina Lulla Jelena Asari Jaan Aarik Kaupo Kukli Raul Rammula Unto Tapper Eero Kauppinen Väino Sammelselg 《Mikrochimica acta》2006,155(1-2):195-198
Quantitative electron probe microanalysis of highly insulating materials is a complicated problem, partially solved by coating
samples with grounded thin conductive layers or using novel scanning electron microscopy (SEM) techniques, such as low-voltage
and/or variable pressure SEM. In this work, some problems of quantitative X-ray microanalysis of thin HfO2 films, in particular the possibility to determine mass thickness correlated to the density of the layer material, are discussed.
For comparison, Al2O3, Ta2O5 and TiO2 films grown onto both semiconductive Si and insulating quartz substrates were also analysed. All the films studied were synthesized
by atomic layer deposition method. 相似文献
5.
Esko K. Pohjala 《Journal of heterocyclic chemistry》1978,15(6):955-960
3-Indolizinyl acetates and propionates 4 react with ethylenic and acetylenic ketones or carboxylic esters to give 1-acylpyrrolo[2,1,5-cd]indolizines 5-12 in excellent yields. 相似文献
6.
7.
8.
Esko Taskinen 《Structural chemistry》1998,9(6):411-418
The spatial structures of a number of mono- and disubstituted 1,1-dimethoxycyclohexanes (cyclohexanone dimethyl acetals) were studied by 13C NMR spectroscopy. In the monosubstituted acetals, substituents (Me, Et, i-Pr, and MeO) on C-2 are axially oriented, contrary to their normal, equatorial orientation on C-3 and C-4. Besides the spectroscopic study, the relative thermodynamic stabilities of the cis-trans isomers of a few 2,X-dialkyl (X = 3, 4, 5, or 6) derivatives of the parent cyclohexanone dimethyl acetal were determined by acid-catalyzed chemical equilibration in MeOH solution. In the most stable isomeric form, the 2-substituent is axial and the other equatorial. In the less stable isomer, both substituents are equatorial, excluding the cis-2,6-dimethyl derivative, where the 13C NMR shift data point to a predominance of the diaxial form. In general, the enthalpy difference between the isomeric forms is ca. 9 kJ mol–1, while the entropy term favors the less stable isomer by 4 to 16 J K–1 mol–1. In the 2,6-dimethyl derivatives, however, the trans form is favored by only 0.8 kJ mol–1 in G
m
at 298.15 K. The main findings of the experimental work are in good agreement with ab initio calculations. 相似文献
9.
The relative thermodynamic stabilities of 24 pairs of carbon-carbon double-bondexo-endo isomeric 2-substituted 4-methylene-1,3-dioxolanes (a) and 4-methyl-1,3-dioxoles (b) have been determined by base-catalyzed chemical equilibration in DMSO solution. In all cases, theendo isomer (b) is the favored species at thermodynamic equilibrium. A single alkyl substitutent on C-2 gives only a negligible contribution to the relative stability of the isomeric forms, but the presence of two alkyl groups on C-2 increases the relative stability of theendo isomer by 2–3 kL mol–1. A still higher effect in favor of theendo isomer is produced by introduction of a single alkoxy group on C-2; this effect is further slightly accentuated by 2,2-dialkoxy substitution at C-2. The origin of the favorable effect of 2-alkoxy substitution on the relative stability of theendo isomer is not clear, but it seems to arise from an unexpected stability of theendo isomer rather than from an enhanced destabilization of theexo form. 相似文献
10.
Laihia K Kolehmainen E Nevalainen T Kauppinen R Vasilieva TT Terentiev AB 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2000,56(3):541-546
The radical addition reactions of organobromine compounds, XBr (X = CH2COOMe, PhCH2, CHBr2 and CCl3) with cyclohexene afforded mixtures of cis/trans isomer pairs of 1-X-2-Br-cyclohexanes. In addition to benzyl benzoyloxy derivatives are formed also, when benzoyl peroxide is used as an initiator. Owing to the great difficulties in separating these cis/trans isomer pairs, they are identified directly in their mixtures by NMR spectroscopy. In addition to one-dimensional (ID) 1H, proton decoupled 13C and DEPT-135, also two-dimensional (2D) 13C-13C INADEQUATE as well as 1H-13C HMQC experiments have been used in assigning the signals of each compound in their mixtures. The identification of each isomer was based on comparison of experimental 3J(H,H) coupling constants with theoretical ones based on the well-known Karplus type relationship. The more stable conformation for each isomer was estimated using the semiempirical AM1 molecular orbital method. The calculations support the isomer pair elucidations. 相似文献