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91.
We present results about minimization of convex functionals defined over a finite set of vectors in a finite-dimensional Hilbert
space, that extend several known results for the Benedetto-Fickus frame potential. Our approach depends on majorization techniques.
We also consider some perturbation problems, where a positive perturbation of the frame operator of a set of vectors is realized
as the frame operator of a set of vectors which is close to the original one. 相似文献
92.
Carla Maria Mariano Fernandez Maurício Ferreira da Rosa Ana Claudia Aparecida Mariano Fernandez Wanessa de Campos Bortolucci Fabiana Borges Padilha Ferreira Giani Andrea Linde 《Natural product research》2020,34(5):731-735
AbstractThis study, was to evaluate the acaricidal effect of the essential oil (EO) and fractions (FR) obtained from Laurus nobilis leaves on Rhipicephalus (Boophilus) microplus. Eight fractions were obtained, however FR1: sabinene (37.83%), β-pinene (13.50%), 1,8-cineole (12.66%), α-pinene (12.56%) and FR8: α-terpineol (79.19%) were highlighted as to the larvicidal potential when submitted by Larval Packet Test. The EO was tested by the Adult Immersion Test, at concentrations of 200.00; 100.00 and 50.00?µL/mL caused mortality of engorged females, egg mass reduction and hatching inhibition. Two fractions are shown to be efficient in controlling larvae FR8 (LC50?=?0.13?µL/mL, LC99?=?0.51?µL/mL) and FR1 (LC50?=?0.20?µL/mL, LC99?=?0.56?µL/mL). The fractionation of EO was determinant to elucidate which compounds were responsible for the larvicidal potential. This study opens new perspectives to direct new bioassays with the compounds obtained in the fractionation, since they present high potential on cattle tick larvae. 相似文献
93.
The sensing of a chemical environment is achieved mainly in the surface by interactions of the sensor material with its chemical surroundings. Therefore, porous structure control is key in developing good chemical sensors. The aim of this work was to obtain materials of tailored porosity to be used as support matrix for optical chemical sensors. We studied the simultaneous effect of pH, temperature, ethanol:TEOS, and water:TEOS molar ratios on gelation time, and textural and structural properties. We used a 24 factorial design that evaluates the effect of each independent variable and their interactions. Samples were characterized by XRD, SEM, FTIR, and gas adsorption (N2 at 77 K and CO2 at 273 K). The gelation time decreased with increasing temperature, water:TEOS molar ratio, and pH; and with decreasing ethanol:TEOS molar ratios. Synthesis conditions also affected the xerogels porous textures. Xerogels obtained at pH 2.5 were ultramicroporous. In general, samples synthesized at pH 4.5 and ethanol:TEOS molar ratio of 2.25:1 were mesoporous, but the material is not appropriate for use as support in fiber optical sensors. 相似文献
94.
Bizzarri M Cavaliere C Foglia P Guarino C Samperi R Laganà A 《Analytical and bioanalytical chemistry》2008,391(5):1969-1976
A label-free absolute quantitation method based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
(MALDI-TOF MS) has been developed. This methodology was applied to mouse heart in order to quantify cardiac troponin T (cTnT),
which is considered to be a sensitive marker of heart damage. The cTnT was extracted, isolated by reversed-phase high-performance
liquid chromatography, digested, and analyzed by MALDI-TOF MS. The MS-based quantitation was performed using matrix-matched
calibration curves (due to a matrix effect) of two synthetic peptides, one cTnT-specific peptide and one internal standard
peptide, respectively. Recoveries at three spiking levels ranged from 87–96%, with relative standard deviations of below 10%.
The method detection limit and the method quantitation limit, expressed as the amount of cTnT for the amount of total sarcomeric
protein extract, were 0.03 mg g−1 and 0.15 mg g−1, respectively. This method appears to be accurate and generally suitable for improving absolute protein quantitation. 相似文献
95.
Skabara PJ Pozo-Gonzalo C Lardiés Miazza N Laguna M Cerrada E Luquin A González B Coles SJ Hursthouse MB Harrington RW Clegg W 《Dalton transactions (Cambridge, England : 2003)》2008,(23):3070-3079
A series of new metal (M) dithiolene complexes bearing terthiophene (3, 12, M = Ni; 4, M = Pd; 5, 6, M = Au) and 2,5-bis(para-methoxyphenyl)thiophene units (14, M = Ni; 15, 16, M = Au; 17, M = Pd) have been synthesised in 38-99% yield. The electrochemical properties of the materials have been characterised by cyclic voltammetry and UV-vis spectroelectrochemistry. The nickel complexes possess low oxidation potentials (-0.12 to -0.25 V vs Ag/AgCl) due to the electron-rich dithiolene centres and all complexes display ligand-based redox activity. The terthiophene derivatives have been polymerised by electrochemical oxidation to give stable films with, in the case of poly(3), broad absorption characteristics. Charge transfer materials have been isolated from 14 and 16 with conductivities in the range 9 x 10(-6) to 7 x 10(-8) S cm(-1). 相似文献
96.
Gianfranco Bocchinfuso Claudia Mazzuca Claudio Saracini Mariano Venanzi Laura Micheli Giuseppe Palleschi Antonio Palleschi 《Mikrochimica acta》2008,163(3-4):195-202
The water soluble 4-sulfocalix[n]arenes (with n?=?4,6,8) have been investigated as potential synthetic receptors for cyclodiene organochlorine pesticides. Steady state fluorescence experiments in ethanol solution have shown that only the cavitands with n equal to 6 and 8 form complexes, of comparable stability, with heptachlor. Electrochemical data, obtained in water solution, confirmed the ability of 4-sulfocalix[6]arene to bind the heptachlor, unlike the smaller calixarene. Moreover, a significant increase in the stability constant is observed in water solutions. This stability is caused by the sterical hindrance of pesticides with respect to the cavity dimension of the calixarene. This results in a selective interaction of this molecule with other organochlorine pesticides. Binding experiments, carried out with endosulfan have shown that, despite of chemical similarity, 4-sulfocalix[6]arene and 4-sulfocalix[8]arene behave in a very different way: the former is unable to bind this pesticide, while the latter shows a binding constant of 4.7?×?105 with endosulfan. To investigate the molecular features of the interactions, molecular dynamic simulations of 4-sulfocalix[6]arene in presence of heptachlor in water solution have been performed. These simulations show that different configurations of heptachlor inside the calixarene cavity are equally populated and easily interconverting, suggesting that a non specific hydrophobic interaction plays a key role in the complex stability. These studies have permitted to individuate versatile synthetic receptors for organochlorine pesticides. 相似文献
97.
The behavior of the cationic hemicyanines trans-4-[4-(dimethylamino)-styryl]-1-methylpyridinium iodide (HC) and 4,(4-(dihexadecylamino)styryl-N-methyl-pyridinium iodide (DIA) were studied in large unilamellar vesicles (LUV) of 1,2-di-oleoyl-sn-glycero-3-phosphatidylcholine (DOPC) using absorption, emission, depolarization and time resolved spectroscopies. Also, thorough spectroscopic studies were performed in homogeneous media to investigate the different interactions that the dyes can experience with its microenvironment. These results help us to comprehend the dye performance under different media and, consequently find interesting features of the DOPC membrane properties. The studies in homogeneous media analyzed by the Kamlet and Taft's solvatochromic comparison method demonstrate, for the first time, that the cationic hemycianines undergo specific interactions with the medium through the solvents ability to donate an electron pair as measured by the beta parameter. Thus, the absorption bands shifts bathochromically with beta while, the emission band shifts hypsochromically. In addition, for the relaxed hemicyanines the 00 energy, nu00, is invariant with the solvent properties. The results in LUV of DOPC show that, DIA undergoes a strong association with the vesicle bilayer while HC partitions between the water and the bilayer pseudophases. To monitor directly the microenvironment and dynamics around HC and DIA inside the DOPC bilayer, we use the wavelength-selective fluorescence approach, which is based on the red edge effect in fluorescence spectroscopy, in addition with the nu00 energy of the hemicyanines. The results show that the fluid state of the DOPC bilayer resembles the microenvironment of sodium bis (2-ethylhexyl) sulfosuccinate (AOT) reverse micelles at W=[H2O]/[AOT] below 10 where there is no free water forming the water pool. Moreover, it is demonstrated for the first time, that the region of the bilayer close to the polar head of DOPC is a powerful electron donor environment. 相似文献
98.
Patricia H. Risso Domingo Mariano Borraccetti César Araujo María Eugenia Hidalgo Carlos A. Gatti 《Colloid and polymer science》2008,286(12):1369-1378
κ-Casein (κ-CN) aggregation by heating has been studied at pH 7.2 and 5.2 using UV-visible spectrophotometry, sodium dodecyl
sulfate polyacrylamide gel electrophoresis, spectrofluorometric study of the 1–8 aniline naphtalene sulfonate (ANS)–κ-CN binding
and circular dichroism (CD) spectroscopy. The aggregation process to form aggregates like micelles or submicelles and the
structural characteristics of these aggregates were pH dependent. Far-UV CD showed that the aggregates obtained by heating
presented changes in the κ-CN secondary structure. Near-UV CD spectra showed a certain degree of tertiary organization in
the Tyr environment for the protein heated or unheated, only at pH 5.2. ANS binding at both pH was quite different and depends
on the self-association process. Heating produced exposition of hydrophobic binding sites only at pH 7.2, including those
in the neighborhood of the κ-CN Trp residue. 相似文献
99.
Biasutti MA Abuin EB Silber JJ Correa NM Lissi EA 《Advances in colloid and interface science》2008,136(1-2):1-24
The effect of surfactants, both in water-in-oil microemulsions (hydrated reverse micelles) and aqueous solutions upon enzymatic processes is reviewed, with special emphasis on the effect of the surfactant upon the kinetic parameters of the process. Differences and similarities between processes taking place in aqueous and organic solvents are highlighted, and the main models currently employed to interpret the results are briefly discussed. 相似文献
100.
Silva OF Silber JJ de Rossi RH Correa NM Fernandez MA 《The journal of physical chemistry. B》2007,111(36):10703-10712
The formation of reverse micelles (RMs) of sodium 1,4-bis(2-ethylhexyl)sulfosuccinate (AOT) in n-heptane including two different beta-cyclodextrin (beta-CD) derivatives (hydroxypropyl-beta-CD, hp-beta-CD, and decenyl succinyl-beta-CD, Mod-beta-CD) is reported. Both cyclodextrins can be incorporated into AOT RMs in different zones within the aggregate, while beta-CD cannot. Using UV-vis and induced circular dichroism (ICD) spectroscopy and different achiral molecular probes (some azo dyes, p-nitroaniline and ferrocene), it was possible to determine that Mod-beta-CD is located with its cavity at the oil side of the AOT RM interface, while for hp-beta-CD the cavity is inside the RM water pool. Among the molecular probes used, methyl orange (MO) was the only one which gave the ICD signal when dissolved in the AOT RMs with hp-beta-CD, so a detailed study of MO behavior in homogeneous media was also performed to compare with the microheterogeneous media. The solvatochromic behavior of the dye depends not only on the polarity of the media but also on other specific solvent properties. A Kamlet-Taft analysis shows that the MO absorption spectrum shifts to longer wavelength with an increase in the solvent polarity-polarizability (pi*) and the hydrogen donor ability (alpha) of the medium. MO appears to be almost 3 times more sensitive to the pi* parameter than to the alpha parameter. In addition, from the MO absorption spectral changes with the hp-beta-CD concentration, the association equilibrium constants in pure water (K11W) and inside the RMs (K11RM) were computed. The results show that K11W is almost 10 times larger than the value inside the RMs. The latter can be explained considering that MO resides anchored to the RM interface through hydrogen bond interaction with the hydration bound water. This study shows for the first time that the cyclodextrin chiral cavity is available for a guest in an organic medium such as the RMs; therefore, we have created a potentially powerful nanoreactor with two different confined regions in the same aggregate: the polar core of the RMs and the chiral hydrophobic cavity of cyclodextrin. 相似文献