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201.
Rosane Aguiar da Silva San Gil Magaly Giro Albuquerque Ricardo Bicca de Alencastro Angelo da Cunha Pinto Fabiano do Espírito Santo Gomes Tereza Neuma de Castro Dantas Maria Aparecida Medeiros Maciel 《Journal of Molecular Structure》2008,885(1-3):82-88
Solid-state 13C nuclear magnetic resonance (13C NMR) with magic-angle spinning (MAS) and with cross-polarization and magic-angle spinning (CP/MAS) spectra, and differential scanning calorimetry (DSC) techniques were used to obtain structural data from a sample of acetyl aleuritolic acid (AAA) extracted from the stem bark of Croton cajucara Benth. (Euphorbiaceae) and recrystallized from acetone. Since solid-state 13C NMR results suggested the presence of more than one molecule in the unitary cell for the AAA, DSC analysis and molecular modeling calculations were used to access this possibility. The absence of phase transition peaks in the DSC spectra and the dimeric models of AAA simulated using the semi-empirical PM3 method are in agreement with that proposal. 相似文献
202.
Rob C. P. Verpaalen Marina Pilz da Cunha Tom A. P. Engels Michael G. Debije Prof. Albert P. H. J. Schenning 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(11):4562-4566
Arbitrary shape (re)programming is appealing for fabricating untethered shape-morphing photo-actuators with intricate configurations and features. We present re-programmable light-responsive thermoplastic actuators with arbitrary initial shapes through spray-coating of polyethylene terephthalate (PET) with an azobenzene-doped light-responsive liquid crystal network (LCN). The initial geometry of the actuator is controlled by thermally shaping and fixing the thermoplastic PET, allowing arbitrary shapes, including origami-like folds and left- and right-handed helicity within a single sample. The thermally fixed geometries can be reversibly actuated through light exposure, with fast, reversible area-specific actuation such as winding, unwinding and unfolding. By shape re-programming, the same sample can be re-designed and light-actuated again. The strategy presented here demonstrates easy fabrication of mechanically robust, recyclable, photo-responsive actuators with highly tuneable geometries and actuation modes. 相似文献
203.
Anizelli PR Vilcachagua JD Neto AC Tormena CF 《The journal of physical chemistry. A》2008,112(37):8785-8789
Conformational preferences for 2-substituted methylenecyclohexanes were determined using (3) J H 2 H 3 spin-spin coupling constants, while stereoelectronic interactions were obtained by means of theoretical calculations and NBO analysis. The conformational equilibrium of compounds studied can be represented by their axial and equatorial conformers, the axial conformers being the most stable form in polar and nonpolar solvents. These conformational preferences were attributed to the hyperconjugative interactions between the pi C-C-->sigma* C-Xax. and sigma C-H-->sigma* C-Xax. orbitals, and the repulsive steric interaction observed between sigma C-H-->n Xeq.. 相似文献
204.
Rob C. P. Verpaalen Marina Pilz da Cunha Tom A. P. Engels Michael G. Debije Albert P. H. J. Schenning 《Angewandte Chemie (International ed. in English)》2020,59(11):4532-4536
Arbitrary shape (re)programming is appealing for fabricating untethered shape‐morphing photo‐actuators with intricate configurations and features. We present re‐programmable light‐responsive thermoplastic actuators with arbitrary initial shapes through spray‐coating of polyethylene terephthalate (PET) with an azobenzene‐doped light‐responsive liquid crystal network (LCN). The initial geometry of the actuator is controlled by thermally shaping and fixing the thermoplastic PET, allowing arbitrary shapes, including origami‐like folds and left‐ and right‐handed helicity within a single sample. The thermally fixed geometries can be reversibly actuated through light exposure, with fast, reversible area‐specific actuation such as winding, unwinding and unfolding. By shape re‐programming, the same sample can be re‐designed and light‐actuated again. The strategy presented here demonstrates easy fabrication of mechanically robust, recyclable, photo‐responsive actuators with highly tuneable geometries and actuation modes. 相似文献
205.
Marina Pilz da Cunha Akhil R. Peeketi Adithya Ramgopal Prof. Ratna K. Annabattula Prof. Albert P. H. J. Schenning 《ChemistryOpen》2020,9(11):1149-1152
Achieving oscillatory motion in polymers without requiring on/off switching of stimuli is a current challenge. Hereby, a free-standing liquid crystal polymer (LCP) is demonstrated to undergo a sustained oscillatory motion when triggered by light, moving back and forth, resembling the motion of a rocking-chair. Two polymer films having different azobenzene photo-switches have been studied, revealing photoswitch requirements as well as illumination conditions necessary to sustain oscillations. The motion presented here shows how feedback loops involving light-triggered actuation, self-shadowing and a shifting center of gravity can be utilized to achieve self-sustained motion in free-standing polymers. 相似文献
206.
Ribeiro LA Neto PH da Cunha WF Roncaratti LF Gargano R Filho DA e Silva GM 《The Journal of chemical physics》2011,135(22):224901
Exciton dissociation and charge recombination processes in organic semiconductors, with thermal effects taken into account, are described in this paper. Here, we analyzed the mechanisms of polaron-excitons dissociation into free charge carriers and the consequent recombination of those carriers under thermal effects on two parallel π-conjugated polymers chains electronically coupled. Our results suggest that exciton dissociation in a single molecule give rise to localized, polaron-like charge carrier. Besides, we concluded that in the case of interchain processes, the bimolecular polaron recombination does not lead to an usual exciton state. Rather, this type of recombination leads to an oscillating dipole between the two chains. The recombination time obtained here for these processes are in agreement with the experimental results. Finally, our results show that temperature effects are essential to the relaxation process leading to polaron formation in a single chain, as in the absence of temperature, this process was not observed. In the case of two chains, we conclude that temperature effects also help the bimolecular recombination process, as observed experimentally. 相似文献
207.
da Silva CH Sobrinho TJ e Castro VT Lima Dda C de Amorim EL 《Molecules (Basel, Switzerland)》2011,16(6):4728-4739
The aims of this study were to quantify the phenolic content and evaluate the antioxidant potential of extracts from the bark and leaves of C. pyramidalis and S. glandulosum. The total phenolic content (TPC) and total tannin content (TTC) were determined using the Folin-Ciocalteu method, and the total flavonoids content (TFC) was measured via complexation with aluminum chloride. The antioxidant activity was evaluated with DPPH (2.2-diphenyl-1-picrylhydrazyl) and FIC (ferrous ion chelating) assays. The TPC ranged between 135.55 ± 9.85 and 459.79 ± 11.65 tannic acid equivalents (TAE) in mg/g material (mg TAE/g). The leaves of both species contained high levels of tannins and flavonoids. The crude ethanol extracts (CEE) from the bark of C. pyramidalis showed high antioxidant activity when compared to ascorbic acid and rutin, whereas the CEE from the leaves was more efficient in chelating ferrous ions. C. pyramidalis had very high phenolic content and anti-radical activity, which indicates a need for further studies aimed at the purification and identification of compounds responsible for the antioxidant activity. 相似文献
208.
Wesley C. Silva Polyana F. Pereira Mariana C. Marra Denise T. Gimenes Rafael R. Cunha Rodrigo A. B. da Silva Rodrigo A. A. Munoz Eduardo M. Richter 《Electroanalysis》2011,23(12):2764-2770
In this work, we report a simple and novel strategy for simultaneous analysis using flow injection analysis with multiple pulse amperometric (FIA‐MPA) detection. The proposed strategy was successfully used for simultaneous determination of paracetamol and caffeine (model analytes) in pharmaceutical formulations. A sequence of potential pulses (waveform) was selected in such a way that PA is selectively oxidized at E1 (+1.20 V/50 ms) and both compounds (PA+CA) are simultaneously oxidized at E2 (+1.55 V/50 ms); hence, current subtraction (using a correction factor) can be used for the selective determination of CA. The proposed FIA method is simple, cheap, fast (140 injections h?1), and present selectivity for the determination of both compounds in pharmaceutical samples, with results similar to those obtained by HPLC at a 95 % confidence level. 相似文献
209.
PVA-Hydrogel Entrapped <Emphasis Type="Italic">Candida Guilliermondii</Emphasis> for Xylitol Production from Sugarcane Hemicellulose Hydrolysate 总被引:1,自引:0,他引:1
da Cunha MA Converti A Santos JC Ferreira ST da Silva SS 《Applied biochemistry and biotechnology》2009,157(3):527-537
Viable cells of Candida guilliermondii were immobilized by inclusion into polyvinyl alcohol (PVA) hydrogel using the freezing–thawing method. Entrapment experiments
were planned according to a 23 full factorial design, using the PVA concentration (80, 100, and 120 g L−1), the freezing temperature (−10, −15, and −20 °C), and the number of freezing-thawing cycles (one, three, and five) as the
independent variables, integrated with three additional tests to estimate the errors. The effectiveness of the immobilization
procedure was checked in Erlenmeyer flasks as the pellet capability to catalyze the xylose-to-xylitol bioconversion of a medium
based on sugarcane bagasse hemicellulosic hydrolysate. To this purpose, the yield of xylitol on consumed xylose, xylitol volumetric
productivity, and cell retention yield were selected as the response variables. Cell pellets were then used to perform the
same bioconversion in a stirred tank reactor operated at 400 rpm, 30 °C, and 1.04 vvm air flowrate. At the end of fermentation,
a maximum xylitol concentration of 28.7 g L−1, a xylitol yield on consumed xylose of 0.49 g g−1 and a xylitol volumetric productivity of 0.24 g L−1 h−1 were obtained. 相似文献
210.
Andr Barreto Cunha Ronan Batista María ngeles Castro Jorge Mauricio David 《Molecules (Basel, Switzerland)》2021,26(4)
Betulinic acid (BA, 3β-hydroxy-lup-20(29)-en-28-oic acid) is a pentacyclic triterpene acid present predominantly in Betula ssp. (Betulaceae) and is also widely spread in many species belonging to different plant families. BA presents a wide spectrum of remarkable pharmacological properties, such as cytotoxic, anti-HIV, anti-inflammatory, antidiabetic and antimicrobial activities, including antiprotozoal effects. The present review first describes the sources of BA and discusses the chemical strategies to produce this molecule starting from betulin, its natural precursor. Next, the antiprotozoal properties of BA are briefly discussed and the chemical strategies for the synthesis of analogues displaying antiplasmodial, antileishmanial and antitrypanosomal activities are systematically presented. The antiplasmodial activity described for BA was moderate, nevertheless, some C-3 position acylated analogues showed an improvement of this activity and the hybrid models—with artesunic acid—showed the most interesting properties. Some analogues also presented more intense antileishmanial activities compared with BA, and, in addition to these, heterocycles fused to C-2/C-3 positions and amide derivatives were the most promising analogues. Regarding the antitrypanosomal activity, some interesting antitrypanosomal derivatives were prepared by amide formation at the C-28 carboxylic group of the lupane skeleton. Considering that BA can be produced either by isolation of different plant extracts or by chemical transformation of betulin, easily obtained from Betula ssp., it could be said that BA is a molecule of great interest as a starting material for the synthesis of novel antiprotozoal agents. 相似文献