全文获取类型
收费全文 | 629篇 |
免费 | 37篇 |
专业分类
化学 | 537篇 |
晶体学 | 1篇 |
力学 | 4篇 |
数学 | 70篇 |
物理学 | 54篇 |
出版年
2023年 | 4篇 |
2022年 | 19篇 |
2021年 | 30篇 |
2020年 | 24篇 |
2019年 | 26篇 |
2018年 | 12篇 |
2017年 | 15篇 |
2016年 | 21篇 |
2015年 | 32篇 |
2014年 | 36篇 |
2013年 | 41篇 |
2012年 | 53篇 |
2011年 | 48篇 |
2010年 | 30篇 |
2009年 | 19篇 |
2008年 | 43篇 |
2007年 | 29篇 |
2006年 | 36篇 |
2005年 | 29篇 |
2004年 | 42篇 |
2003年 | 28篇 |
2002年 | 20篇 |
2001年 | 4篇 |
2000年 | 4篇 |
1999年 | 2篇 |
1998年 | 5篇 |
1997年 | 1篇 |
1996年 | 6篇 |
1995年 | 1篇 |
1994年 | 4篇 |
1993年 | 1篇 |
1987年 | 1篇 |
排序方式: 共有666条查询结果,搜索用时 15 毫秒
591.
D. Donescu S. Serban Kristina Gosa Simon Moscu Maria Zaharescu 《Journal of Dispersion Science and Technology》2013,34(5):559-570
The modification of the rate or formation of interpenetrant simultaneous inorsjanic-organic (SIPIN) networks of poly(vinyl acetate) (PVAc)-SiO; was studied. The P(VAc) network was formod by radical polymerization with benzoyl peroxide in the presence of a crosslinked monomer, diethylen glycol bis maleate. SiO: network was obtained by sol-gel reaction of tetraethoxysilane (TEOS) catalyzed by radical polymeriznble acids: maleic acid (MA) and acrylic acid (AA) The reaction medium was the ethylic alcohol-water mixture. The formation rate of SIPIN depends on the ratio of initial organic over aqueous phases in case of caialysis by MA. The yelling limes for MA are higher than those for AA. This behavior inversely proponional to the acid strength is assigned to the selective interaction of the acids wiih the hydrocarbonated or aqueous zone of initial systems. Crotonic acid (CrA) is partitioned in the hydrocarbonate zone where TEOS also lies The glass transition temperature of organic network, P(VAc) increases with the increase of crosslinking agent concentration. It is higher in the network prepared in presence of MA owing to the higher number of hydrogen bonds induced by COOH. 相似文献
592.
Kristina Kristinaityte Mateusz Urbaczyk Adam Mames Mariusz Pietrzak Tomasz Ratajczyk 《Molecules (Basel, Switzerland)》2021,26(21)
Anthracenes are an important class of acenes. They are being utilized more and more often in chemistry and materials sciences, due to their unique rigid molecular structure and photoreactivity. In particular, photodimerization can be harnessed for the fabrication of novel photoresponsive materials. Photodimerization between the same anthracenes have been investigated and utilized in various fields, while reactions between varying anthracenes have barely been investigated. Here, Nuclear Magnetic Resonance (NMR) spectroscopy is employed for the investigation of the photodimerization of two exemplary anthracenes: anthracene (A) and 9-bromoanthracene (B), in the solutions with only A or B, and in the mixture of A and B. Estimated k values, derived from the presented kinetic model, showed that the dimerization of A was 10 times faster in comparison with B when compounds were investigated in separate samples, and 2 times faster when compounds were prepared in the mixture. Notably, the photoreaction in the mixture, apart from AA and BB, additionally yielded a large amount of the AB mixdimer. Another important advantage of investigating a mixture with different anthracenes is the ability to estimate the relative reactivity for all the reactions under the same experimental conditions. This results in a better understanding of the photodimerization processes. Thus, the rational photofabrication of mix-anthracene-based materials can be facilitated, which is of crucial importance in the field of polymer and material sciences. 相似文献
593.
Kristina Prir Ema Horak Marijeta Kralj Lidija Uzelac Sandra Liekens Ivana Murkovi Steinberg Svjetlana Kritafor 《Molecules (Basel, Switzerland)》2022,27(3)
In this work, a series of novel 1,2,3-triazolyl-coumarin hybrid systems were designed as potential antitumour agents. The structural modification of the coumarin ring was carried out by Cu(I)-catalysed Huisgen 1,3-dipolar cycloaddition of 7-azido-4-methylcoumarin and terminal aromatic alkynes to obtain 1,4-disubstituted 1,2,3-triazolyl-coumarin conjugates 2a–g, bis(1,2,3-triazolyl-coumarin)benzenes 2h–i and coumarin-1,2,3-triazolyl-benzazole hybrids 4a–b. The newly synthesised hybrid molecules were investigated for in vitro antitumour activity against five human cancer cell lines, colon carcinoma HCT116, breast carcinoma MCF-7, lung carcinoma H 460, human T-lymphocyte cells CEM, cervix carcinoma cells HeLa, as well as human dermal microvascular endothelial cells (HMEC-1). Most of these compounds showed moderate to pronounced cytotoxic activity, especially towards MCF-7 cell lines with IC50 = 0.3–32 μM. In addition, compounds 2a–i and 4a–b were studied by UV-Vis absorption and fluorescence spectroscopy and their basic photophysical parameters were determined. 相似文献
594.
Kristina Wickholm Eva-Lena Hult Per Tomas Larsson Tommy Iversen Helena Lennholm 《Cellulose (London, England)》2001,8(2):139-148
In this paper, we present a chemometric model for quantifying the cellulose forms with different states of order found within cellulose I fibrils. The relative amounts of the different cellulose forms, that is crystalline cellulose I, para-crystalline cellulose and cellulose at accessible and inaccessible cellulose surfaces, were determined by non-linear least squares fitting of the C4-region in CP/MAS 13C-NMR (Cross-Polarisation Magic Angle Spinning Carbon-13 Nuclear Magnetic Resonance) spectra. By correlating these results from the C4-region with the full spectral data we obtained a model which is able to provide an assessment of the relative amounts of the different cellulose forms directly from NMR-spectra of complex lignocellulosic samples. Furthermore, this model enabled new assignments to be made in the C1-region for signals from cellulose at accessible fibril surfaces. 相似文献
595.
596.
597.
Kristina Elg Christoffersson Michael Sjöström Ulf Edlund Åsa Lindgren Matti Dolk 《Cellulose (London, England)》2002,9(2):159-170
The reactivity of dissolving pulp was experimentally determined in termsof residual cellulose in viscose. The correlations between 11 chemicalproperties of pulp and filter values and residual cellulose contents of viscosewere then investigated by multivariate data analysis. Both the viscose filtervalue and the residual cellulose were well modelled from the 11 propertiesby partial least squares regression. The results show that pulps with highacetone extractable fractions, high magnesium contents, low alkali resistanceand low viscosity, gave low viscose filter values and low residual cellulosecontents. Pulps with low residual cellulose contents also had low carboxylgroupcontents and low polydispersity. The results are interpreted as that in pulpwith high reactivity, the hemicellulose content is low and that the cellulosechains are shorter and more soluble in alkali. An explanation of the positiveeffect from the high extractive content is that the extractives facilitate thediffusion of carbon disulfide. A principal component analysis of CP/MAS13C-NMR spectral data of six pulp samples showed that differences inreactivity between the pulps could be explained by variations in the hydrogenbonds in the cellulose and/or changes in the glucosidic bonds. In a separatestudy electron beam processing enhanced the reactivity, i.e. lowered theresidual cellulose content, of the investigated pulps. The magnitude of theelectron dose, within the tested range (5.4–23.7 kGy), didnotseem to be important, but the reactivity within pulp sheets tended to be ratherinhomogeneous. 相似文献
598.
Hoffmann K Blaudszun J Brunken C Höpker WW Tauber R Steinhart H 《Analytical and bioanalytical chemistry》2005,381(6):1138-1144
To clarify the mechanism of the anticarcinogenic effect of conjugated linoleic acid (CLA), its intracellular distribution needs to be determined. Subcellular fractionation using centrifugation techniques is a method that is frequently used for isolation of cell organelles from different tissues. But as the size and density of the organelles differ, the method needs to be optimised for every type of tissue. The novelty of this study is the application of a subcellular fractionation method to human healthy and cancerous renal and testicular tissue. Separation of total tissue homogenate into nuclei, cytosol, and a mixture of mitochondria and plasma membranes was achieved by differential centrifugation. As mitochondria and plasma membranes seemed to be too similar in size and weight to be separated by differential centrifugation, discontinuous density-gradient centrifugation was carried out successfully. The purity of the subcellular fractions was checked by measuring the activity of marker enzymes. All fractions were highly enriched in their corresponding marker enzyme. However, the nuclear fractions of kidney and renal cell carcinoma were slightly contaminated with mitochondria and plasma membrane fractions of all tissues with lysosomes. The fraction designated the cytosolic fraction contained not only cytosol, but also microsomes and lysosomes. The CLA contents of the subcellular fractions were in the range 0.13–0.37% of total fatty acids and were lowest in the plasma membrane fractions of all types of tissue studied. C16:0, C18:0, C18:1 c9, C18:2 n-6, and C20:4 n-6 were found to be the major fatty acids in all the subcellular fractions studied. However, marked variations in fatty acid content between subcellular fractions and between types of tissue were detectable. Because of these differences between tissues, no general statement on characteristic fatty acid profiles of single subcellular fractions is possible. 相似文献
599.
Ma S Caprioli RM Hill KE Burk RF 《Journal of the American Society for Mass Spectrometry》2003,14(6):593-600
Characterization of reduced and alkylated rat selenoprotein P by mass spectrometry yielded selenopeptides from which one or more selenium atoms were missing. Predicted selenopeptide mass peaks were accompanied by peaks corresponding to the conversion of one or more selenocysteine residues to dehydroalanine(s). Experiments were carried out to determine whether this loss of selenium occurred in vitro. A selenopeptide was isolated that contained two selenocysteine residues that were both in selenide-sulfide linkages with cysteine residues. After the peptide had been reduced and alkylated, in addition to the predicted mass peak with both selenocysteine residues present, two mass peaks were detected at positions expected for conversion of one and two selenocysteine residues of this selenopeptide to dehydroalanine residues, which was confirmed by tandem mass spectrometry. Similar findings were obtained from a study of another selenoprotein, rat plasma glutathione peroxidase. These results indicate that selenium atoms are lost from selenoproteins during purification and characterization. The loss of selenium from selenoproteins is probably through the mechanism of oxidation of selenocysteine residue to selenoxide followed by syn-beta-elimination of selenenic acid during sample processing. 相似文献
600.
Hansen KK Grosch B Greiveldinger-Poenaru S Bartlett PA 《The Journal of organic chemistry》2003,68(22):8465-8470
Lactams 1 and 2 are readily formed from acyclic precursors in the presence of trypsin and chymotrypsin, respectively, identifying the macrocyclic ring system as a potential motif for constrained transition state analogue inhibitors of the serine peptidases. Ketone 3 was synthesized and shown to be a modest inhibitor of chymotrypsin (Ki = 220 microM), albeit 4-fold more potent than the acyclic hydroxy acid 25 (Ki = 1.5 mM as a mixture of epimers). A precursor (31) to the amino boronic acid 4 was also prepared; although this derivative was a potent inhibitor of chymotrypsin (Ki = 130 nM) by virtue of the boronic acid moiety, it showed no advantage over the des-amino analogue 32 (Ki = 120 nM), which is not capable of cyclizing. 相似文献