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排序方式: 共有84条查询结果,搜索用时 15 毫秒
1.
Carla M. Bossu Edilene C. Ferreira Fernanda S. Chaves Eveline A. Menezes Ana Rita A. Nogueira 《Microchemical Journal》2006,84(1-2):88-92
A flow injection system was proposed to evaluate the transient product of a colorimetric reaction between hydrolysable tannin and potassium iodate (KIO3) solution. The system optimization was accomplished by using statistical methods based on experimental design. Flow rate of KIO3 solution, sample volume, carrier flow rate, and reaction coil were the selected factors for evaluation. On screening step, complete factorial 24 was used and two levels for each selected factor were studied. For the optimization phase, a centered face composite design 22 + star was employed to evaluate sample volume and flow rate of KIO3 solution, which were the factors identified in the screening phase as having more influence on the absorbance signal. After optimization, the proposed system was compared with batch determination. Some characteristics, such as analytical frequency, reagent consumption and chemical residues generation presented better results by the use of the proposed system if compared with batch method. The system presented good repeatability with standard deviation lower than 3%, for n = 10, linearity (R2 = 0.9974) for tannic acid standard, analytical frequency of 15 injections h− 1 and limit of quantification of 24 mg L− 1 of tannic acid. Good results were obtained when the proposed system was applied to hydrolysable tannin determination in Stryphnodendron barbatimão, Eucalyptus citriodora and Phyllanthus niruri, samples of plants commonly used in popular medicine. 相似文献
2.
Background
Hundreds of extracellular proteins polymerise into filaments and matrices by using zona pellucida (ZP) domains. ZP domain proteins perform highly diverse functions, ranging from structural to receptorial, and mutations in their genes are responsible for a number of severe human diseases. Recently, PLAC1, Oosp1-3, Papillote and CG16798 proteins were identified that share sequence homology with the N-terminal half of the ZP domain (ZP-N), but not with its C-terminal half (ZP-C). The functional significance of this partial conservation is unknown. 相似文献3.
Franziska Back Matthias Bockmeyer Eveline Rudigier-Voigt Peer Löbmann 《Journal of Sol-Gel Science and Technology》2013,66(1):73-83
Hybrid polymer solutions suitable for UV-nanoimprint were synthesized by combination of an alkoxysilane binder mixture with silica nanoparticles. Hydrolysis and condensation reactions were monitored by NMR and viscosity measurements. Thereby long-term stable systems were produced as a prerequisite for industrial application. Dip-coating of glass substrates and subsequent UV-curing yielded thin films. Their thermal densification and microstructural evolution resulted in pure glassy porous coatings, which were in detail characterized by N2-sorption measurements and ellipsometric porosimetry. Results emphasize the importance of the binder-particle interaction within these materials that are destined for the fabrication of microstructured surfaces by cost efficient and industrially feasible UV-based soft lithography. Structured glassy layers with high inorganic content show thermal stability up to >500 °C and have a high structure accuracy >85 %. 相似文献
4.
Dr. Shrinivas Dumbre Dr. Valérie Pezo Guy Schepers Prof. Vitor B. Pinheiro Prof. Eveline Lescrinier Prof. Philipp Holliger Dr. Philippe Marlière Prof. Piet Herdewijn 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(13):5009-5022
The synthesis, base‐pairing properties and in vitro and in vivo characteristics of 5‐methyl‐isocytosine (isoCMe) and isoguanine (isoG) nucleosides, incorporated in an HNA(h) (hexitol nucleic acid)–DNA(d) mosaic backbone, are described. The required h‐isoG phosphoramidite was prepared by a selective deamination as a key step. As demonstrated by Tm measurements the hexitol sugar showed slightly better mismatch discrimination against dT. The d‐isoG base mispairing follows the order T>G>C while the h‐isoG base mispairing follows the order G>C>T. The h‐ and d‐isoCMe bases mainly mispair with G. Enzymatic incorporation experiments show that the hexitol backbone has a variable effect on selectivity. In the enzymatic assays, isoG misincorporates mainly with T, and isoCMe misincorporates mainly with A. Further analysis in vivo confirmed the patterns of base‐pair interpretation for the deoxyribose and hexitol isoCMe/isoG bases in a cellular context, through incorporation of the bases into plasmidic DNA. Results in vivo demonstrated that mispairing and misincorporation was dependent on the backbone scaffold of the base, which indicates rational advances towards orthogonality. 相似文献
5.
Alloyed catalysts receive considerable attention, because of their unique catalytic properties; they often show higher selectivity, activity, and stability compared to the pure metal particles. To provide insights in the origins of these features, we report the structure and the interaction of hydrogen with each of the metals in an intimately mixed platinum-gold catalyst and compare these characteristics to those in the single metal particles. X-Ray absorption spectroscopy (XAS) and electron microscopy analysis showed that the structure of the mixed particle differed from the single metal particles. The interaction of platinum with hydrogen is stronger than the H-Au interaction and the adsorption sites were different. EXAFS analysis showed that the structure of the platinum clusters changes with increasing hydrogen coverage, observed as a relaxation of the contracted Pt-Pt distance and an increase in the Pt-Pt coordination number. No such changes were observed for gold clusters. Well-mixed PtAu-alloy clusters, with a bulk Au-to-Pt ratio of two, supported on SiO(2), adsorb hydrogen on both platinum and gold atoms, which indicates that gold cannot be regarded as an inert metal. The heat of adsorption on the platinum ensembles does not decrease upon alloying; the weakening of the overall hydrogen adsorption strength when alloying platinum with gold is an ensemble-size effect. 相似文献
6.
Mi-Yeon Jang Xiao-Ping Song Mathy Froeyen Philippe Marlière Eveline Lescrinier Jef Rozenski Piet Herdewijn 《Chemistry & biology》2013,20(3):416-423
Highlights? A highly modified nucleotide as substrate for polymerases ? The reversibility of the polymerase reaction at the template level ? Synthesis of a nucleoside with two anomeric centers 相似文献
7.
Amit M. Jabgunde Rahul S. Patil Swarup De Eveline Lescrinier Steven De Jonghe Leonid Beigelman Piet Herdewijn 《Tetrahedron》2019,75(8):1107-1114
The synthesis of 3′-fluoro-4′-amino-hexitol nucleosides with a uracil and cytosine nucleobase was performed. The synthesis started from 1,5:2,3-dianhydro-4,6-benzylidene-allitol and afforded the target compounds in 15 steps. These protected hexitol nucleosides are valuable building blocks for the preparation of a new class of oligonucleotides. 相似文献
8.
Eveline De Robertis Gabriela F. Moreira Raigna A. Silva Carlos A. Achete 《Journal of Thermal Analysis and Calorimetry》2011,106(2):347-354
Quality control of fuel-related properties of biodiesel, such as thermal stability, is needed to obtain consistent engine
performance by fuel users, since biodiesel is susceptible to auto-oxidation when exposed to air, light, and temperature during
storage. In this work two pure standard reference materials of biodiesels produced from soy oil and animal feedstocks were
studied. Differential scanning calorimetry and thermogravimetry measurements were performed and the analysis of the results
revealed small temperature variations in the thermal events among the two standards, these differences are due mainly to their
chemical composition, been highly influenced by the amounts of unsaturated esters. 相似文献
9.
10.
Lagoja IM Pochet S Boudou V Little R Lescrinier E Rozenski J Herdewijn P 《The Journal of organic chemistry》2003,68(5):1867-1871
The synthesis of fully [13C/15N] labeled pyrimidine nucleosides has been achieved from 13C-glucose and labeled nucleobases. The reaction scheme leads directly to the protected nucleosides without the need for the inversion of configuration of C-3 of 13C-glucose. This was achieved by an oxitative ring-opening reaction removing the carbon with the wrong configuration. 相似文献