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排序方式: 共有347条查询结果,搜索用时 31 毫秒
51.
Segura Y Chmielarz L Kustrowski P Cool P Dziembaj R Vansant EF 《The journal of physical chemistry. B》2006,110(2):948-955
Vanadium oxide was deposited on mesoporous titania by the molecular designed dispersion method to investigate the potential properties of these catalysts. Mesoporous titania was synthesized following the evaporation-induced self-assembly (EISA) method with a subsequent treatment with ammonia to increase the thermal stability. As a result, the mesoporous titania obtained shows a high surface area (approximately 350 m2/g) and high stability. Vanadium oxide was deposited by the MDD method using a vanadyl acetylacetonate complex that was transformed into VOx after a controlled calcination in air flow at 300 degrees C. The mesostructure and porosity characteristics of titania remain even until the maximum V-loading was reached (0.4 mmol/g), as it was shown by N2 sorption measurements at -196 degrees C. The catalysts were characterized by chemical analysis, Fourier transform infrared-photoacoustic spectroscopy (FTIR-PAS), UV-vis diffuse reflectance (DR), and Fourier transform Raman spectroscopy. Raman spectra showed isolated V species for the different V-containing catalysts. Furthermore, UV-vis-DR revealed a higher contribution of polymeric species as the V loading increases. The VOx/mesoporous titania catalysts were highly active in the selective catalytic reduction of NOx. A high activity in the NO conversion was observed, which increases with increasing metal loading. 相似文献
52.
Giacalone F Segura JL Martín N Ramey J Guldi DM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(16):4819-4834
A series of donor-acceptor arrays (C60-oligo-PPV-exTTF; 16-20) incorporating pi-conjugated oligo(phenylenevinylene) wires (oligo-PPV) of different length between pi-extended tetrathiafulvalene (exTTF) as electron donor and C60 as electron acceptor has been prepared by multistep convergent synthetic approaches. The electronic interactions between the three electroactive species present in 16-20 were investigated by UV-visible spectroscopy and cyclic voltammetry (CV). Our studies clearly show that, although the C60 units are connected to the exTTF donors through a pi-conjugated oligo-PPV framework, no significant electronic interactions are observed in the ground state. Interestingly, photoinduced electron-transfer processes over distances of up to 50 Angstroms afford highly stabilized radical ion pairs. The measured lifetimes for the photogenerated charge-separated states are in the range of hundreds of nanoseconds (approximately 500 ns) in benzonitrile, regardless of the oligomer length (i.e., from the monomer to the pentamer). A different lifetime (4.35 micros) is observed for the heptamer-containing array. This difference in lifetime has been accounted for by the loss of planarity of the oPPV moiety that increases with the wire length, as established by semi-empirical (PM3) theoretical calculations carried out with 19 and 20. The charge recombination dynamics reveal a very low attenuation factor (beta = 0.01 +/- 0.005 Angstroms(-1)). This beta value, as well as the strong electron coupling (V approximately 5.5 cm(-1)) between the donor and the acceptor units, clearly reveals a nanowire behavior for the pi-conjugated oligomer, which paves the way for applications in nanotechnology. 相似文献
53.
A. Segura M. C. Martínez-Tomás B. Marí A. Casanovas A. Chevy 《Applied Physics A: Materials Science & Processing》1987,44(3):249-260
Acceptor levels related to I, II, IV, and V group impurities in indium selenide are studied by means of the Hall effect, deep-level-transient spectroscopy (DLTS) and photoluminescence. Activation energies for hole concentrations in the range from 200 to 300 meV have been measured. A reversible change of sign of the Hall voltage has been observed below 215 K. This behaviour can be explained through a model in which acceptor levels are assumed to be shallow and interlayer planar precipitates of ionized shallow donors create potential wells that behave as deep donors and in which a low concentration of bidimensional free electrons can exist. This model also explains the capacitance-voltage characteristics of both ITO/p-InSe and Au/p-InSe barriers. DLTS results are coherent with this model: hole traps in high concentration located about 570 meV above the valence band are detected. Photoluminescence also confirms the shallow character of acceptor levels. A broad band whose intensity is related to p conductivity appears in the PL spectra of low resistivity p-InSe. The shape and temperature dependence of this band can be explained through self-activated photoluminescence in a complex center in which the ground acceptor level must be at about 50 meV above the valence band. 相似文献
54.
Shaoping Fu David Arráez‐Román Javier A. Menéndez Antonio Segura‐Carretero Alberto Fernández‐Gutiérrez 《Rapid communications in mass spectrometry : RCM》2009,23(1):51-59
In this work, rapid‐resolution liquid chromatography (RRLC) coupled to electrospray ionization time‐of‐flight mass spectrometry (ESI‐TOF‐MS) and ion trap multiple mass spectrometry (IT‐MSn) has been applied to separate and characterize eleven isomers of oleuropein aglycon in fourteen Spanish extra‐virgin olive oils. After the extra‐virgin olive oil sample had been dissolved in hexane and cleaned up by a diol‐bonded phase solid‐phase extraction (SPE) cartridge, the eluting extract was resolved in methanol and analyzed on an Angilent 1200 system with a 4.6 × 150 mm, 1.8 µm Zorbax Eclipse plus C18 column. Mass spectrometry was carried out on a Bruker Daltonics microTOF mass spectrometer and a Bruker Daltonics ion trap mass spectrometer. The characterization of isomers of oleuropein aglycon was based on accurate mass data and the isotope function of characteristic fragment ions in the studied compounds by TOF‐MS, and the fragment ions were further confirmed by IT‐MSn. The fragmentation pathway of oleuropein aglycon was successfully elucidated and all possible transformations among isomers of oleuropein aglycon were suggested. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
55.
Giovanni Dinelli Antonio Segura Carretero Raffaella Di Silvestro Ilaria Marotti Shaoping Fu Stefano Benedettelli Lisetta Ghiselli Alberto Fernández Gutiérrez 《Journal of chromatography. A》2009,1216(43):7229-7240
An evaluation of the grain functional components of Italian durum wheat cultivars was conducted. The raw material was obtained from the field trial performed in 2006–2007 at the Experimental Farm of the University of Bologna, (Bologna, Italy). The aim of this study was to define the phytochemical profile of ten varieties, comprised of old and modern durum wheat genotypes, including quantitative and qualitative phenolic and flavonoid content (free and bound forms). The results showed that mean values of total phenolic compound and total flavonoid content in old wheat varieties (878.2 ± 19.0 μmol gallic acid equivalent/100 g of grain and 122.6 ± 25.4 μmol catechin equivalent/100 g of grain, respectively) did not differ significantly from those detected in modern genotypes (865.9 ± 128.9 μmol gallic acid equivalent/100 g and 123.5 ± 20.6 μmol catechin equivalent/100 g, respectively). However, the HPLC–ESI-TOF-MS analysis highlighted remarkable differences between modern and old cultivars. The interpretation of the mass spectra allowed the identification of 70 phenolic compounds, including coumarins, phenolic acids, anthocyanins, flavones, isoflavones, proanthocyanidins, stilbenes and lignans. The free extracts of ancient wheat varieties showed the presence of a mean number of phenolic compounds and isomer forms (8.7 ± 2.5 and 7.7 ± 4.7 respectively) significantly higher than in modern genotypes (4.4 ± 2.9 and 2.0 ± 2.4, respectively). A similar trend was observed also for the bound phenolic fraction. Moreover, the phytochemical profiles showed the presence of unique phenolic compounds in both free and bound fractions of some of the investigated wheat genotypes. Results highlighted that investigated old wheat cultivars may offer unique nutraceutical values for their peculiar contents in bioactive phytochemicals, suggesting their uses into a wide range of regular and specialty products naturally enriched with health-promoting compounds. 相似文献
56.
Rocío García‐Villalba Alegría Carrasco‐Pancorbo Gabriela Zurek Marina Behrens Carsten Bäßmann Antonio Segura‐Carretero Alberto Fernández‐Gutiérrez 《Journal of separation science》2010,33(14):2069-2078
The applicability of nanoLC‐ESI‐TOF MS for the analysis of phenolic compounds in olive oil was studied and compared with a HPLC method. After the injection, the compounds were focused on a short capillary trapping column (100 μm id, effective length 20 mm, 5 μm particle size) and then nanoLC analysis was carried out in a fused silica capillary column (75 μm id, effective length 10 μm, 3 μm particle size) packed with C18 stationary phase. The mobile phase was a mixture of water + 0.5% acetic acid and ACN eluting at 300 nL/min in a gradient mode. Phenolic compounds from different families were identified and quantified. The quality parameters of the nanoLC method (linearity, LODs and LOQs, repeatability) were evaluated and compared with those obtained with HPLC. The new methodology presents better sensitivity (reaching LOD values below 1 ppb) with less consumption of mobile phases, but worse repeatability, especially inter‐day repeatability, resulting in more difficulties to get highly accurate quantification. The results described in this article open up the application fields of this technique to cover a larger variety of compounds and its advantages will make it especially useful for the analysis of samples containing low concentration of phenolic compounds, as for instance, in biological samples. 相似文献
57.
Testosterone metabolism revisited: discovery of new metabolites 总被引:1,自引:0,他引:1
Oscar J. Pozo Josep Marcos Rosa Ventura Andreu Fabregat Jordi Segura 《Analytical and bioanalytical chemistry》2010,398(4):1759-1770
The metabolism of testosterone is revisited. Four previously unreported metabolites were detected in urine after hydrolysis
with KOH using a liquid chromatography–tandem mass spectrometry method and precursor ion scan mode. The metabolites were characterized
by a product ion scan obtained with accurate mass measurements. Androsta-4,6-dien-3,17-dione, androsta-1,4-dien-3,17-dione,
17-hydroxy-androsta-4,6-dien-3-one and 15-androsten-3,17-dione were proposed as feasible structures for these metabolites
on the basis of the mass spectrometry data. The proposed structures were confirmed by analysis of synthetic reference compounds.
Only 15-androsten-3,17-dione could not be confirmed, owing to the lack of a commercially available standard. That all four
compounds are testosterone metabolites was confirmed by the qualitative analysis of several urine samples collected before
and after administration of testosterone undecanoate. The metabolite androsta-1,4-dien-3,17-dione has a structure analogous
to that of the exogenous anabolic steroid boldenone. Specific transitions for boldenone and its metabolite 17β-hydroxy-5β-androst-1-en-3-one
were also monitored. Both compounds were also detected after KOH treatment, suggesting that this metabolic pathway is involved
in the endogenous detection of boldenone previously reported by several authors. 相似文献
58.
59.
We find the connected compact domains in the closed half-plane, with fixed area and diameter, which minimize the relative perimeter.This work has been partially supported by the DGICYT (Spain) Grant no. PB 91-0324. 相似文献
60.
Water vapor sensing characterization of a metal resonator fabricated with an industrial 0.35 μm CMOS technology is reported. The resonator frequency is ~13.2 MHz and exhibits a sensitivity magnitude of ~3.5 kHz per %RH without requiring any additional hygroscopic coating layer. An on-chip integrated oscillator circuit enables an unprecedented resolution of 0.005 %RH. 相似文献