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101.
Luisa Célia Melo Sergio Antonio Spinola Machado Djenaine De Souza Adriana Nunes Correia 《Talanta》2009,79(5):1216-1222
This paper describes the use of a dental amalgam electrode (DAE) to evaluate the electrochemical behaviour and to develop an electroanalytical procedure for determination of diquat herbicide in natural water and potato samples. The work was based on the square wave voltammetry responses of diquat, which presented two well-defined and reversible reduction peaks, at −0.56 V (peak 1) and −1.00 V (peak 2). The experimental and voltammetric parameters were optimised, and the analytical curves were constructed and compared to similar curves performed by high performance liquid chromatography coupled to ultraviolet-visible spectrophotometric detector (HPLC/UV-vis). The responses were directly proportional to diquat concentration in a large interval of concentration, and the calculated detection limits were very similar, around 10 μg L−1 (10 ppb) for voltammetric and chromatographic experiments. These values were lower than the maximum residue limit established for natural water by the Brazilian Environmental Agency. The recovery percentages in pure electrolyte, natural water and potato samples showed values from 70% to 130%, demonstrating that the voltammetric methodology proposed is suitable for determining any contamination by diquat in different samples, minimising the toxic residues due to the use of liquid mercury or the adsorptive process relative to use of other solid surfaces. 相似文献
102.
Eliane Gonçalves Gomes João Carlos Correia Baptista Soares de Mello Geraldo da Silva e Souza Lidia Angulo Meza João Alfredo de Carvalho Mangabeira 《Annals of Operations Research》2009,169(1):167-181
The aim of this paper is to use DEA models to evaluate sustainability in agriculture. Several variables are taken into account
and the resulting efficiency is measured by comparison. The performance of family farms is analysed here (variables: farmed
area, work force, and production). As agricultural sustainability depends on the maintenance of systems of production for
long periods of time, the models were run for the years of 1986 and 2002. Tiered DEA models were used to group farmers in
sustainability categories. Non-parametric regression models were used to identify the factors affecting the efficiency measurements.
All the results indicate that the majority of the farmers increased their efficiency along the time. These improvements may
support the existence of sustainability. 相似文献
103.
Pinto V Norberto F Pamplona T Fernandez MT Duarte MF 《Rapid communications in mass spectrometry : RCM》2006,20(15):2309-2316
Electron ionisation mass spectrometry studies were performed previously for p-diphenyl carbonate and some monosubstituted diphenyl carbonates. In this work, p-diphenyl carbonate and p-methoxyphenylphenyl carbonate are re-examined, and p-chlorophenyl phenyl carbonate and two disubstituted diphenyl carbonates, bis (p-chlorophenyl) carbonate and p-methoxyphenyl-p-fluorophenyl carbonate, are studied for the first time. The previously established fragmentation routes were observed for all compounds investigated. Some other different sequences were observed, and a fragmentation path, other than decarboxylation, of the molecular ion is proposed. In the fast-atom bombardment study it was observed that the M(+*)/[MH](+) ion abundance ratio increased from 0.44 for compound 1 to 2.95 for compound 5. [MH](+) is not a dominant ion in most of compounds studied, in spite of the presence of a carbonyl group, a strong proton acceptor. The presence of two oxygen atoms bonded to the carbonyl group appears to induce delocalisation of the electron pairs, thus deactivating the carbonyl site for protonation. In addition, m-nitrobenzyl alcohol (NBA) being a relatively aprotic/hydrophobic matrix reinforces the deactivation for protonation. Because the carbonate group and NBA are common features to the study, the contributions of the substituents were taken into account to explain the different behaviour of the five compounds with respect to protonation. 相似文献
104.
105.
Mohammad‐Ali Shahbazi Patrick V. Almeida Ermei Mkil Alexandra Correia Mnica P. A. Ferreira Martti Kaasalainen Jarno Salonen Jouni Hirvonen Hlder A. Santos 《Macromolecular rapid communications》2014,35(6):624-629
Currently, developing a stable nanocarrier with high cellular internalization and low toxicity is a key bottleneck in nanomedicine. Here, we have developed a successful method to covalently conjugate poly(methyl vinyl ether‐co‐maleic acid) (PMVE‐MA) copolymer on the surface of (3‐aminopropyl)triethoxysilane‐functionalized thermally carbonized porous silicon nanoparticles (APSTCPSi NPs), forming a surface negatively charged nanovehicle with unique properties. This polymer conjugated NPs could modify surface smoothness, charge, and hydrophilicity of the developed NPs, leading to considerable improvement in the colloidal and plasma stabilities via enhanced suspensibility and charge repulsion. Furthermore, despite the surface negative charge of the polymer‐conjugated NPs, the cellular internalization was increased in both MDA‐MB‐231 and MCF‐7 breast cancer cells. These results provide a proof‐of‐concept evidence that such polymer‐based PSi nanocomposite can be extensively used as a promising candidate for intracellular drug delivery.
106.
This review covers the literature on the chemically mediated ecology of cyanobacteria, including ultraviolet radiation protection, feeding-deterrence, allelopathy, resource competition, and signalling. To highlight the chemical and biological diversity of this group of organisms, evolutionary and chemotaxonomical studies are presented. Several technologically relevant aspects of cyanobacterial chemical ecology are also discussed. 相似文献
107.
Mycobacterial pathogenesis is closely associated with a unique cell envelope rich in complex carbohydrates and unique lipids, among which are the mycolic acids. Mycobacteria also synthesize unique intracellular polymethylated polysaccharides (PMPSs), namely methylglucose lipopolysaccharides (MGLPs), which are acylated with short-chain fatty acids, and methylmannose polysaccharides (MMPs). Since PMPSs modulate the synthesis of long-chain fatty acids in vitro, the possibility of a similar role in vivo and the regulation of mycolic acids assembly have been anticipated. Unlike MGLPs, MMPs have been identified in M. smegmatis and other fast-growing mycobacteria but not in M. tuberculosis, implying an essential role for MGLPs in this pathogen and turning the biosynthetic enzymes into attractive drug targets. The genome of M. tuberculosis was decoded 14 years ago but only recently has the identity of the genes involved in MGLPs biosynthesis been investigated. Two gene clusters (Rv1208-Rv1213 and Rv3030-Rv3037c) containing a few genes considered to be essential for M. tuberculosis growth, have initially been proposed to coordinate MGLPs biosynthesis. Among these genes, only the product of Rv1208 for the first step in the MGLPs pathway has, so far, been crystallized and its three-dimensional structure been determined. However, recent results indicate that at least three additional clusters may be involved in this pathway. The functional assignment of authentic roles to some of these M. tuberculosis H37Rv genes sheds new light on the intricacy of MGLPs biogenesis and renewed interest on their biological role. 相似文献
108.
Brustein VP Cavalcanti CL de Melo-Junior MR Correia MT Beltrão EI Carvalho LB 《Applied biochemistry and biotechnology》2012,166(2):268-275
Nowadays, there is an increase of investigations into the fibroadenoma, mainly because some studies have shown that the occurrence
of fibroadenoma is linked to an increased risk of developing breast carcinoma. Currently, the chemiluminescence biomarkers
are applied for validation methods and screening. Here, a lectin chemiluminescence is proposed as new histochemistry method
to identify carbohydrates in mammary tumoral tissues. The lectins concanavalin A (Con A) and peanut agglutinin (PNA) conjugated
to acridinium ester were used to characterize the glycocode of breast tissues: normal, fibroadenoma, and invasive duct carcinoma
(IDC). The lectin chemiluminescence expressed in relative light units (RLU) was higher in fibroadenoma and IDC than in normal
tissue for both lectins tested. The relationship RLU emission versus tissue area described a linear and hyperbolic curve for
IDC and fibroadenoma, respectively, using Con A whereas hyperbolic curves for both transformed tissues using PNA. RLU was
abolished by inhibiting the interaction between tissues and lectins using their specific carbohydrates: methyl-α-d-mannoside (Con A) and galactose (PNA). The intrinsic fluorescence emission did not change with combination of the lectins
(Con A/PNA) to the acridinium ester for hydrophobic residues. These results represent the lectin chemiluminescence as an alternative
of histochemistry method for tumoral diagnosis in the breast. 相似文献
109.
Catarina I. V. Ramos M. Graça Santana‐Marques A. J. Ferrer‐Correia Joana F. B. Barata Augusto C. Tomé M. Graça P. M. S. Neves J. A. S. Cavaleiro Paulo E. Abreu Mariette M. Pereira Alberto A. C. C. Pais 《Journal of mass spectrometry : JMS》2012,47(4):516-522
Two new isomeric aminomethyl corrole derivatives of [5,10,15‐tris(pentafluorophenyl)corrolato]gallium(III) were synthesized with pyridine (py) molecules as axial ligands. When investigated by electrospray ionization mass spectrometry, in the positive and the negative ion modes, these compounds showed an unusual gas‐phase behavior that could be used for their differentiation. In the positive ion mode, the differentiation was achieved through the formation of diagnostic fragment ions formed from [M‐py + H]+ precursors, by (CH3)2NH and HF losses. An unusual addition of water to the main fragment ions provides an alternative route for isomer identification. Semi‐empirical calculations were performed to elucidate the structures and stabilities of the main ionic species formed in the positive ion mode. In the negative ion mode isomer discrimination is accomplished via the fragmentation of the methoxide adduct ions [M‐py + CH3O]‐ through (CH3)2 N. and HF losses. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
110.
Teresa Avilés António Dinis Michael G. B. Drew Vitor Félix 《Monatshefte für Chemie / Chemical Monthly》2000,6(1):1305-1310
The self-assembly of Ag[BF4] with trans-azobenzene in dichloromethane yields a new coordination polymer ([Ag(μ-trans-azobenzene)H2O][BF4])n which was characterized by X-ray single crystal diffraction. The crystal consists of 1-D zigzag cationic chains made up from [Ag(H2O)]+ units linked by trans-azobenzene bridges and BF− 4 anions. Hydrogen bonding interactions between the chains and BF− 4 anions occur via intermolecular C*H⋯F and O*H⋯F contacts, and the crystal displays a 2-D supramolecular structure. 相似文献