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991.
Textile/Metal–Organic‐Framework Composites as Self‐Detoxifying Filters for Chemical‐Warfare Agents 下载免费PDF全文
Elena López‐Maya Dr. Carmen Montoro Dr. L. Marleny Rodríguez‐Albelo Dr. Salvador D. Aznar Cervantes Dr. A. Abel Lozano‐Pérez Prof. José Luis Cenís Dr. Elisa Barea Prof. Jorge A. R. Navarro 《Angewandte Chemie (International ed. in English)》2015,54(23):6790-6794
The current technology of air‐filtration materials for protection against highly toxic chemicals, that is, chemical‐warfare agents, is mainly based on the broad and effective adsorptive properties of hydrophobic activated carbons. However, adsorption does not prevent these materials from behaving as secondary emitters once they are contaminated. Thus, the development of efficient self‐cleaning filters is of high interest. Herein, we report how we can take advantage of the improved phosphotriesterase catalytic activity of lithium alkoxide doped zirconium(IV) metal–organic framework (MOF) materials to develop advanced self‐detoxifying adsorbents of chemical‐warfare agents containing hydrolysable P? F, P? O, and C? Cl bonds. Moreover, we also show that it is possible to integrate these materials onto textiles, thereby combining air‐permeation properties of the textiles with the self‐detoxifying properties of the MOF material. 相似文献
992.
Inside Cover: Textile/Metal–Organic‐Framework Composites as Self‐Detoxifying Filters for Chemical‐Warfare Agents (Angew. Chem. Int. Ed. 23/2015) 下载免费PDF全文
993.
Computational Study of Proton Transfer in Tautomers of 3‐ and 5‐Hydroxypyrazole Assisted by Water 下载免费PDF全文
Dr. Cristina Trujillo Dr. Goar Sánchez‐Sanz Prof. Ibon Alkorta Prof. José Elguero 《Chemphyschem》2015,16(10):2140-2150
The tautomerism of 3‐ and 5‐hydroxypyrazole is studied at the B3LYP, CCSD and G3B3 computational levels, including the gas phase, PCM–water effects, and proton transfer assisted by water molecules. To understand the propensity of tautomerization, hydrogen‐bond acidity and basicity of neutral species is approached by means of correlations between donor/acceptor ability and H‐bond interaction energies. Tautomerism processes are highly dependent on the solvent environment, and a significant reduction of the transition barriers upon solvation is seen. In addition, the inclusion of a single water molecule to assist proton transfer decreases the barriers between tautomers. Although the second water molecule further reduces those barriers, its effect is less appreciable than the first one. Neutral species present more stable minima than anionic and cationic species, but relatively similar transition barriers to anionic tautomers. 相似文献
994.
Simultaneous Aromatic–Beryllium Bonds and Aromatic–Anion Interactions: Naphthalene and Pyrene as Models of Fullerenes,Carbon Single‐Walled Nanotubes,and Graphene 下载免费PDF全文
Dr. Marta Marín‐Luna Prof. Ibon Alkorta Prof. José Elguero Prof. Otilia Mó Prof. Manuel Yáñez 《Chemphyschem》2015,16(12):2680-2686
The possibility of forming stable BeR2:ArH:Y? (R=H, F, Cl; ArH=naphthalene, pyrene; Y=Cl, Br) ternary complexes in which the beryllium compounds and anions are located on the opposite sides of an extended aromatic system is explored by means of MP2/aug‐cc‐pVDZ ab initio calculations. Comparison of the electron‐density distribution of these ternary complexes with the corresponding BeR2:ArH and ArH:Y? binary complexes reveals the existence of significant cooperativity between the two noncovalent interactions in the triads. The energetic effects of this cooperativity are quantified by evaluation of the three‐body interaction energy Δ3E in the framework of the many‐body interaction‐energy (MBIE) approach. Although an essential component of the interaction energies is electrostatic and is well reflected in the changes in the molecular electrostatic potential of the aromatic system on complexation, strong polarization effects, in particular for the BeR2:ArH interactions, also play a significant role. The charge transfers associated with these polarization effects are responsible for significant distortion of both the BeR2 and the aromatic moieties. The former are systematically bent in all the complexes, and the latter are curved to a degree that depends on the nature of the R substituents of the BeR2 subunit. 相似文献
995.
UV Emission of Gd3+ in the Presence of Cu2+: Towards Luminescence Quenching through Quantum Cutting? 下载免费PDF全文
Dr. José A. Jiménez 《Chemphyschem》2015,16(8):1683-1686
The first investigation into the ultraviolet (UV) photoluminescence of gadolinium(III) in the presence of copper(II) is reported. A melt‐quenched barium phosphate glass was used as a model matrix. The optical spectroscopy assessment shows that with increasing CuO concentration the Cu2+ absorption band grows steadily, whereas the UV emission from Gd3+ ions is progressively quenched. The data, thus, suggests the existence of a Gd3+→Cu2+ energy‐transfer process ocurring through quantum cutting. A downconversion/cross‐relaxation pathway proceeding through a virtual state in Gd3+ is proposed. These findings suggest gadolinium(III) could potentially be used in the optical sensing of copper(II). 相似文献
996.
Gonzalo Martínez‐García Verónica Serafín Lourdes Agüí Paloma Yáñez‐Sedeño José M. Pingarrón 《Electroanalysis》2015,27(5):1119-1126
An electrochemical immunosensor for ghrelin (GHRL) determination in saliva is reported. Anti‐GHRL was immobilized onto Protein G‐magnetic beads and a competitive immunoassay involving biotinylated GHRL and alkaline phosphatase‐streptavidin was implemented. Once conjugate was magnetically captured on a screen‐printed carbon electrode, GHRL quantization was accomplished by DPV of 1‐naphtol formed upon addition of 1‐naphtyl phosphate. A linear range between 10?3 and 103 ng/mL GHRL, and a LOD of 7 pg/mL, much smaller than those from commercial ELISA kits, were found. The usefulness of the immunosensor was demonstrated by analyzing human saliva spiked with GHRL at 0.01, 0.1, 1 and 10 ng/mL. 相似文献
997.
José E. Báez Ángel Marcos-Fernández 《International Journal of Polymer Analysis and Characterization》2015,20(7):637-644
The biodegradable aliphatic oligoesters polyglycolide (PGA), poly(L-lactide) (PLLA), and poly(?-caprolactone) (PCL) with similar number-average molecular weight Mn values but different linear alkyl end groups [CH3?[CH2?CH2]m?CH2?] were compared in terms of their physical properties, parameters such as melting temperature (Tm), crystallinity (xi), long period (L), and lamella thickness (D). They were analyzed by DSC and SAXS. The effect of a longer and nonpolar alkyl end group such as docosyl [CH3?[CH2?CH2]10?CH2?] on the long period (L) was more evident for PCL because it was the most nonpolar species in the family of oligoesters analyzed. 相似文献
998.
Suellen Christtine da Costa Sanches Flávio de Vasconcelos Carlos Emmerson Ferreira da Costa Patrícia Santana Barbosa Marinho Marcos R. Guilherme Eraldo José Madureira Tavares José Antônio Picanço Diniz Júnior José Otávio Carréra Silva Júnior Roseane Maria Ribeiro-Costa 《Journal of Thermal Analysis and Calorimetry》2015,120(1):991-999
999.
1000.
Supercritical fluid chromatography with photodiode array detection for pesticide analysis in papaya and avocado samples 下载免费PDF全文
Norma S. Pano‐Farias Silvia G. Ceballos‐Magaña Jorge Gonzalez José M. Jurado Roberto Muñiz‐Valencia 《Journal of separation science》2015,38(7):1240-1247
To improve the analysis of pesticides in complex food matrices with economic importance, alternative chromatographic techniques, such as supercritical fluid chromatography, can be used. Supercritical fluid chromatography has barely been applied for pesticide analysis in food matrices. In this paper, an analytical method using supercritical fluid chromatography coupled to a photodiode array detection has been established for the first time for the quantification of pesticides in papaya and avocado. The extraction of methyl parathion, atrazine, ametryn, carbofuran, and carbaryl was performed through the quick, easy, cheap, effective, rugged, and safe methodology. The method was validated using papaya and avocado samples. For papaya, the correlation coefficient values were higher than 0.99; limits of detection and quantification ranged from 130–380 and 220–640 μg/kg, respectively; recovery values ranged from 72.8–94.6%; precision was lower than 3%. For avocado, limit of detection values were ?450 μg/kg; precision was lower than 11%; recoveries ranged from 50.0–94.2%. Method feasibility was tested for lime, banana, mango, and melon samples. Our results demonstrate that the proposed method is applicable to methyl parathion, atrazine, ametryn, and carbaryl, toxics pesticides used worldwide. The methodology presented in this work could be applicable to other fruits. 相似文献