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181.
AbstractBacterial cellulose (BC) is an extracellular natural polymer produced by many microorganisms and its properties could be tailored via specific fabrication methods and culture conditions. There is a growing interest in BC derived materials due to the main features of BC such as porous fibrous structure, high crystallinity, impressive physico-mechanical properties, and high water content. However, pristine BC lacks some features, limiting its practical use in varied applications. Thus, fabrication of BC composites has been attempted to overcome these constraints. This review article overviews most recent advance in the development of BC composites and their potential in biomedicine including wound dressing, tissue engineering scaffolds, and drug delivery. Special emphasis is placed on the fabrication and applications of BC-containing nanofibrous composites for biomedical usage. It summarizes electrospinning of BC-based nanofibers and their surface modification with an outline on challenges and future perspective. 相似文献
182.
Sidra Amin Aneela Tahira Amber R. Solangi Raffaello Mazzaro Zafar Hussain Ibupoto Almas Fatima Alberto Vomiero 《Electroanalysis》2020,32(5):1052-1059
Nickel oxide (NiO) nanostructures are employed in the basic medium for the oxidation of ethanol. A variety of NiO nanostructures are synthesized by wet chemical growth method, using different hydroxide (OH?) ion sources, particularly from ammonia, hexamethylenetetramine, urea and sodium hydroxide. The use of urea as (OH?) ion source results in flower‐like NiO structures composed by extremely thin nanowalls (thickness lower than 10 nm,), which demonstrated to be the most active for ethanol oxidation. All the samples exhibit NiO cubic phase, and no other impurity was detected. The cyclic voltammetry (CV) curves of NiO nanostructures were found linear over the concentration range 0.1–3.5 mM (R2=0.99) of ethanol, with the limit of detection estimated to be 0.013 mM for ethanol. The NiO nanostructures exhibit a selective signal towards ethanol oxidation in the presence of different members of alcohol family. The proposed NiO nanostructures showed a significant practicality for the reproducible and sensitive determination of ethanol from brandy, whisky, mixture of brandy and rum, and vodka samples. The nanomaterial was used as a surface modifying agent for the glassy carbon electrode and it showed a stable electro‐oxidation activity for the ethanol for 16 days. These findings indicate that the presented NiO nanomaterial can be applied in place of noble metals for ethanol sensing and other environmental applications (like fuel cells). 相似文献
183.
Ajmal Khan Heng Zhao Meina Zhang Shahid Khan Depeng Zhao 《Angewandte Chemie (International ed. in English)》2020,59(3):1340-1345
Chiral sulfones are of great importance in medicinal chemistry and chemical synthesis. Efficient methods for preparing enantiomerically enriched sulfone‐containing molecules can therefore be of significant value; such methods, however, are uncommon. Herein, we report the first general palladium‐catalyzed sulfonylation of vinyl cyclic carbonates with sodium sulfinates. A series of enantiomerically enriched tertiary allylic sulfones were synthesized in good yields with excellent enantiomeric ratios. Both aliphatic‐ and aryl‐substituted vinyl cyclic carbonates are suitable reactants with excellent results. This reaction features broad substrates scope, readily available starting materials, excellent regio‐ and enantioselectivity, and synthesis of sulfone‐bearing quaternary carbon stereocenters. Through the sulfonylation of geranyl derived cyclic carbonate 1 h , we achieve the formal total synthesis of (+)‐agelasidine A. 相似文献
184.
Basma H. Amin Mohamed I. Abou-Dobara Mostafa A. Diab Essam A. Gomaa Mohammed A. El-Mogazy Adel Z. El-Sonbati Mohamed S. EL-Ghareib Mostafa A. Hussien Hanaa M. Salama 《应用有机金属化学》2020,34(8):e5689
A novel series of mixed-ligand complexes of 5,5′-{(1E,1E′)-1,4-phenelynebis(diazene-2,1-diyl)}bis(quinolin-8-ol) (H2L1) as a primary ligand and 4-aminoantipyrine(L2) as a secondary ligand with Mn(II) ion were prepared using two general formulae: [Mn2(H2L1)2(L2)2X4].4Cl (X = OH2( 1 ), ONO2−( 2 ), Cl=nil; OAc( 3 ), Cl = nil) and [Mn2(H2L1)(L2)2(O2SO2)2]( 4 ). Free ligands and their complexes were characterized. Electronic absorption spectra of the mixed-ligand complexes indicate a distorted octahedral geometry around the central metal ion, and the anions X− are in the axial positions for all compounds. The ligands behave in a neutral bidentate manner, through nitrogen atoms and oxygen atoms of the carbonyl group (L2), whereas H2L1 coordinated through nitrogen and OH groups as a neutral bidentate ligand. All complexes do not contain coordinated water molecules, but complex ( 1 ) contains four water molecules. The water molecules are removed in a single step. The complexes exhibited magnetic susceptibility corresponding to five unpaired electrons. The antimicrobial activity of the Mn(II) mixed-ligand complexes ( 1–4 ) against two gram-positive bacteria, three local gram-negative bacteria, and three fungi species was tested. Mn(II) mixed-ligand complex ( 2 ) exhibited significant antibacterial activity against Bacillus cereus, Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Pseudomonas sp. Mixed-ligand complex ( 2 ) exhibited a high potential cytotoxicity against the growth of human lung cancer cells. 相似文献
185.
Malak Azmat Ali G. Murtaza Afzal Khan Eman Algrafy Asif Mahmood Shahid M. Ramay 《International journal of quantum chemistry》2020,120(19):e26357
Highly spin-polarized ferromagnetic materials are essential for efficient spintronic devices. Here, 100% spin-polarized compounds Rb2TaZ6 (Z = Cl, Br) studied via density functional theory are reported. These compounds show stability in the ferromagnetic phase with cubic symmetry and half metallic behavior, thereby exhibiting a nonzero direct band gap in the spin-down channel and zero band gap in the spin-up configuration. The Ta-d sates contribute mainly to the net magnetic moments as explained by the crystal field theory and density of states. High Curie temperatures of 960.35 and 1021.74 K for Ra2TaCl6 and Rb2TaBr6, along with maximum spin polarizability, make these compounds favorable for efficient spintronic applications. 相似文献
186.
Peilin Deng Fan Yang Zhitong Wang Shenghua Chen Yinzheng Zhou Shahid Zaman Prof. Dr. Bao Yu Xia 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(27):10899-10905
Carbon dioxide (CO2) conversion is promising in alleviating the excessive CO2 level and simultaneously producing valuables. This work reports the preparation of carbon nanorods encapsulated bismuth oxides for the efficient CO2 electroconversion toward formate production. This resultant catalyst exhibits a small onset potential of −0.28 V vs. RHE and partial current density of over 200 mA cm−2 with a stable and high Faradaic efficiency of 93 % for formate generation in a flow cell configuration. Electrochemical results demonstrate the synergistic effect in the Bi2O3@C promotes the rapid and selective CO2 reduction in which the Bi2O3 is beneficial for improving the reaction kinetics and formate selectivity, while the carbon matrix would be helpful for enhancing the activity and current density of formate production. This work provides effective bismuth-based MOF derivatives for efficient formate production and offers insights in promoting practical CO2 conversion technology. 相似文献
187.
Wafaa M. Abdou Neven A. Ganoub Amin F. Fahmy Abeer A. Shaddy 《Monatshefte für Chemie / Chemical Monthly》2006,46(10):105-116
Two simple and efficient one-pot procedures for the synthesis of a series of α-branched N-heterocycle-substituted methane-1,1-bisphosphonates
are outlined. In the first method, the parent halosubstrates were reacted with cyanomethylphosphonate followed by reaction
with dialkyl phosphonates to give asymmetrical or symmetrical bisphosphonates (BPs). In the second approach, the same halocompounds were reacted with tetraethyl methyl-1,1-bisphosphonate to give the requisite
BPs. Partial and complete hydrolysis of the prepared BPs were also investigated. The products contain functional groups advantageous for further synthetic modification as structural
units for coupling with the drug. 相似文献
188.
Alaa S. Amin Ibrahim S. Ahmed Hassan A. Dessouki Hassan A. Mohamed 《Chemical Papers》2010,64(3):278-284
Simple and rapid spectrophotometric methods have been developed for the microdetermination of fluoxetine HCl. The proposed
methods are based on the formation of ion-pair complexes between fluoxetine and bromophenol blue (BPB), bromothymol blue (BTB),
bromocresol green (BCG), and bromocresol purple (BCP) which can be measured at optimum λmax. Optimization of reaction conditions was investigated. Beerșs law was obeyed in the concentration ranges of 0.5–8.0 μg mL−1, whereas optimum concentration as adopted from the Ringbom plots was 0.7–7.7 μg mL−1. The molar absorptivity, Sandell sensitivity, and detection limit were also calculated. The most optimal and sensitive method
was developed using BCG. The correlation coefficient was 0.9988 (n = 6) with a relative standard deviation of 1.25, for six determinations of 4.0 μg mL−1. The proposed methods were successfully applied to the determination of fluoxetine hydrochloride in its dosage forms and
in biological fluids (spiked plasma sample) using the standard addition technique. 相似文献
189.
A highly sensitive spectrophotometric method for palladium determination using piroxicam and tenoxicam as new chromogenic
reagents has been developed. In the presence of sodium lauryl sulfate (SLS), palladium reacts with piroxicam (PX) or tenoxicam
(TX) to form stable yellow orange complexes in an acetate buffer solution of pH 5.0 at 424 nm and 426 nm with molar absorptivity
of 7.16 × 104 L mol−1 cm−1 and 1.20 × 105 L mol−1 cm−1, respectively. Sandell sensitivity, detection, and quantitation limits were also calculated. Optimum conditions were evaluated
considering pH, reagent concentration, time, temperature, and surfactant concentration. The complex system conforms to Beer’s
law over the range of 0.07–1.28 μg mL−1 palladium. The stoichiometric ratio and stability constant were also evaluated. Tolerance limits of many cations and anions
were determined. Finally, the proposed method was applied successfully in the determination of palladium in jewellery, anode
mud, synthetic mixtures, catalysts, and alloy samples. 相似文献
190.
M. S. Al-Masri Y. Amin B. Al-Akel T. Al-Naama 《Applied biochemistry and biotechnology》2010,160(4):976-987
The removal of metal ions from aqueous solutions by biosorption plays an important role in water pollution control. In this
study, dried leaves and branches of poplar trees were studied for removing some toxic elements (cadmium, lead, and uranium)
from aqueous solutions. The equilibrium experiments were systematically carried out in a batch process, covering various process
parameters that include agitation time, adsorbent size and dosage, initial cadmium, lead and uranium concentration, and pH
of the aqueous solution. Adsorption behavior was found to follow Freundlich and Langmuir isotherms. The results have shown
that both dried leaves and branches can be effectively used for removing uranium, while only branches were found to remove
lead and cadmium completely from the aqueous solution. The maximum biosorption capacity of leaves for uranium was found to
be 2.3 mg g−1 and 1.7 mg g−1 and 2.1 mg g−1 for lead and cadmium on branches, respectively. In addition, the studied biomass materials were used in removing lead and
cadmium from contaminated water and the method was found to be effective. 相似文献