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101.
102.
The direct patterning of poly(p‐methoxyphenylmethylsilane) (PMPMS) and poly(p‐methoxyphenylmethylgermane) (PMPMG) by interference lithography is reported. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
103.
Robson Miranda da Gama Tatiana Santana Balogh Simone França Tânia Cristina Sá Dias Valcinir Bedin André Rolim Baby Jivaldo do Rosário Matos Maria Valéria Robles Velasco 《Journal of Thermal Analysis and Calorimetry》2011,106(2):399-405
This research aimed the effect on Caucasian hair tresses treated with oxidative hair dye, either incorporated or not with
conditioners agents, analyzed by Differential Scanning Calorimetry (DSC) and Thermogravimetric analysis (TG). The formulations
of hair dyes were emulsions oil-in-water with light blond color containing or not the conditioners agents: silanetriol and
panthenol; PEG-12 dimethicone; hydrolyzed silk, hydrolyzed milk protein, and lactose. Each dye (1.5 g) was applied in the
hair tress (2.0 g/20.0 cm of length of Caucasian light-brown), previously treated, more 1.5 g of hydrogen peroxide 20 vol
during 40 min. Evaluation of mass loss of the different hair sample demonstrates that these chemical hair treatments impair
the hair fibers, reduced their moisture content with respect to the untreated hair. The incorporation of conditioners agents
(silanetriol and panthenol; PEG-12 dimethicone; hydrolyzed silk, hydrolyzed milk protein, and lactose) in oxidative hair dyes
types did not decrease the damage caused on the tresses by the coloring process quantified by TG/DTG. However, the DSC curves
demonstrated those conditioners agents (silanetriol and panthenol; PEG-12 dimethicone) dislocated the beginning of the third
event in 20 °C and they inhibited the presence of the fourth event, having characterized thermal protection to the hair. 相似文献
104.
105.
A reinvestigation of the reactions of urea derivatives of diaminomaleonitrile 2 with aldehydes or ketones in the presence of triethylamine has established that the products of these reactions are not pyrimidino[5,4-d]pyrimidines 9 as previously reported, but 8-oxo-6-carboxamido-1,2-dihydropurines 12, which are oxidized rapidly in air to the corresponding 6-carboxamidopurines 13. Similarly, the reaction of Schiff base derivatives of DAMN 5 with isocyanates in the presence of triethylamine gives the substituted 2-oxoimidazoles 20 and not the pyrimidine derivatives 8 as previously claimed. The compounds 20 cyclize in solution and are easily oxidized to 8-oxopurine-6-carbonitriles 22, which give the same 8-oxopurine-6-carboxamides 13 upon further hydrolysis. 相似文献
106.
Caio L. Firme Andrei V. Grafov Marcos L. Dias 《Journal of polymer science. Part A, Polymer chemistry》2005,43(18):4248-4259
Ethylene and propylene polymerization using Ind2ZrCl2 and Ind2Zr(CH3)2/MAO catalytic systems modified by the sterically demanding bridged alicyclic alcohols, adamantan‐1‐ol, adamantan‐2‐ol, 2‐methyladamantan‐2‐ol, and fenchyl alcohol, was investigated. Lower alcohols like isopropanol completely deactivate the system, whereas in the case of catalysts modified by these voluminous alcohols only a slight decrease in the catalytic activity proportional to alcohol/metallocene molar ratio was observed. The addition of the modifiers gives rise to polymers with higher molecular weights than the nonmodified systems, but no structural changes in the polyethylenes were observed. The addition of the sterically demanding alcohols to the reaction medium changes the regioregularity of polypropylenes, but does not significantly influence their stereoregularity, at 30 °C. Propylene–ethylene copolymers containing up to 8.6% of ethylene units derived from 1,3‐insertion and significant amount of rr‐centered pentads were obtained by single‐monomer polymerization of propylene with Ind2ZrCl2/MMAO/adamantan‐1‐ol, at 70 °C. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4248–4259, 2005 相似文献
107.
Ana Cristi B Dias 《Analytica chimica acta》2004,514(2):253-257
A sequential injection system with spectrophotometric detection was proposed for the determination of copper, zinc and lead in brass. In view of the high analyte concentrations and the sensitivity of the involved catalytic methods, optimization of the flow system was carried out aiming mild reaction conditions. Copper and lead determinations were based on the catalytic effects of Cu2+ and Pb2+ on the oxidation rates of resorcinol and pyrogallol red by H2O2, respectively, and zinc determination involved precipitate formation after oxidation of 1-nafthylethylenediamine by K3Fe(CN)6. The analytical procedures were designed with some common parameters such as pH=9.0 (borate system), λ=530 nm, and H2O2 as oxidizing agent; system geometry was maintained.The proposed system is rugged, and base line drift is not observed during 4 h operation periods. Twenty samples are run per hour (60 determinations) and reagent consumption is minimal, thus avoiding drawbacks related to waste management. Precise results (R.S.D.<1.0%; n=7) are obtained and a detection limit of 1% (w/w) was estimated for the three analytes. Results were in agreement with flame atomic absorption spectrometry. 相似文献
108.
H.-D. Pfannes D. S. Vieira Junior R. Paniago J. H. Dias Filho 《Hyperfine Interactions》2005,165(1-4):247-252
The formation of local moments and the effect of charge carrriers in dilute magnetic semiconductors can be well understood using local probe techniques like Mossbauer Spectroscopy. We report here on Mossbauer studies in the systems Fe0.008Ge1 ? x D x (D = As, Bi), Fe0.008Ge1 ? x In x , and Fe0.008Ge1 ? x Sn x . At room temperature magnetic interactions were observed for donor (D) impurities at the Fe site in the Fe0.008Ge system. No such magnetic ordering was observed for acceptor (In) or neutral (Sn) impurities. 相似文献
109.
J. Dias de Deus 《Zeitschrift fur Physik C Particles and Fields》1990,46(1):125-128
The effect of leading charges in negative and charged particle distributions in limited rapidity bins is discussed with particular emphasis on the extent in rapidity of strong charge correlations. 相似文献
110.
Dr. Yongjun Zhou Prof. Patrícia Prediger Prof. Luiz Carlos Dias Dr. Annabel C. Murphy Prof. Peter F. Leadlay 《Angewandte Chemie (International ed. in English)》2015,54(17):5232-5235
Elaiophylin is an unusual C2‐symmetric antibiotic macrodiolide produced on a bacterial modular polyketide synthase assembly line. To probe the mechanism and selectivity of diolide formation, we sought to reconstitute ring formation in vitro by using a non‐natural substrate. Incubation of recombinant elaiophylin thioesterase/cyclase with a synthetic pentaketide analogue of the presumed monomeric polyketide precursor of elaiophylin, specifically its N‐acetylcysteamine thioester, produced a novel 16‐membered C2‐symmetric macrodiolide. A linear dimeric thioester is an intermediate in ring formation, which indicates iterative use of the thioesterase active site in ligation and subsequent cyclization. Furthermore, the elaiophylin thioesterase acts on a mixture of pentaketide and tetraketide thioesters to give both the symmetric decaketide diolide and the novel asymmetric hybrid nonaketide diolide. Such thioesterases have potential as tools for the in vitro construction of novel diolides. 相似文献