全文获取类型
收费全文 | 911篇 |
免费 | 97篇 |
国内免费 | 36篇 |
专业分类
化学 | 563篇 |
晶体学 | 3篇 |
力学 | 46篇 |
综合类 | 22篇 |
数学 | 182篇 |
物理学 | 228篇 |
出版年
2023年 | 10篇 |
2022年 | 3篇 |
2021年 | 14篇 |
2020年 | 11篇 |
2019年 | 19篇 |
2018年 | 18篇 |
2017年 | 8篇 |
2016年 | 25篇 |
2015年 | 25篇 |
2014年 | 27篇 |
2013年 | 45篇 |
2012年 | 71篇 |
2011年 | 62篇 |
2010年 | 39篇 |
2009年 | 31篇 |
2008年 | 32篇 |
2007年 | 46篇 |
2006年 | 39篇 |
2005年 | 37篇 |
2004年 | 45篇 |
2003年 | 63篇 |
2002年 | 98篇 |
2001年 | 101篇 |
2000年 | 25篇 |
1999年 | 28篇 |
1998年 | 8篇 |
1997年 | 9篇 |
1996年 | 11篇 |
1995年 | 7篇 |
1994年 | 8篇 |
1993年 | 4篇 |
1992年 | 8篇 |
1991年 | 3篇 |
1990年 | 2篇 |
1989年 | 4篇 |
1988年 | 4篇 |
1985年 | 4篇 |
1984年 | 2篇 |
1983年 | 2篇 |
1982年 | 4篇 |
1981年 | 4篇 |
1980年 | 3篇 |
1979年 | 3篇 |
1978年 | 9篇 |
1976年 | 2篇 |
1975年 | 2篇 |
1973年 | 2篇 |
1938年 | 1篇 |
1908年 | 4篇 |
1907年 | 2篇 |
排序方式: 共有1044条查询结果,搜索用时 15 毫秒
991.
Chavan S Vitillo JG Gianolio D Zavorotynska O Civalleri B Jakobsen S Nilsen MH Valenzano L Lamberti C Lillerud KP Bordiga S 《Physical chemistry chemical physics : PCCP》2012,14(5):1614-1626
The recently discovered UiO-66/67/68 class of isostructural metallorganic frameworks (MOFs) [J. H. Cavka et al. J. Am. Chem. Soc., 2008, 130, 13850] has attracted great interest because of its remarkable stability at high temperatures, high pressures and in the presence of different solvents, acids and bases [L. Valenzano et al. Chem. Mater., 2011, 23, 1700]. UiO-66 is obtained by connecting Zr(6)O(4)(OH)(4) inorganic cornerstones with 1,4-benzene-dicarboxylate (BDC) as linker resulting in a cubic MOF, which has already been successfully reproduced in several laboratories. Here we report the first complete structural, vibrational and electronic characterization of the isostructural UiO-67 material, obtained using the longer 4,4'-biphenyl-dicarboxylate (BPDC) linker, by combining laboratory XRPD, Zr K-edge EXAFS, TGA, FTIR, and UV-Vis studies. Comparison between experimental and periodic calculations performed at the B3LYP level of theory allows a full understanding of the structural, vibrational and electronic properties of the material. Both materials have been tested for molecular hydrogen storage at high pressures and at liquid nitrogen temperature. In this regard, the use of a longer ligand has a double benefit: (i) it reduces the density of the material and (ii) it increases the Langmuir surface area from 1281 to 2483 m(2) g(-1) and the micropore volume from 0.43 to 0.85 cm(3) g(-1). As a consequence, the H(2) uptake at 38 bar and 77 K increases from 2.4 mass% for UiO-66 up to 4.6 mass% for the new UiO-67 material. This value is among the highest values reported so far but is lower than those reported for MIL-101, IRMOF-20 and MOF-177 under similar pressure and temperature conditions (6.1, 6.2 and 7.0 mass%, respectively) [A. G. Wong-Foy et al. J. Am. Chem. Soc., 2006, 128, 3494; M. Dinca and J. R. Long. Angew. Chem., Int. Ed., 2008, 47, 6766]. Nevertheless the remarkable chemical and thermal stability of UiO-67 and the absence of Cr in its structure would make this material competitive. 相似文献
992.
Realistic mechanistic pictures of β-hairpin formation, offering valuable insights into some of the key early events in protein folding, are accessible through short designed polypeptides as they allow atomic-level scrutiny through simulations. Here, we present a detailed picture of the dynamics and mechanism of β-hairpin formation of Chignolin, a de novo decapeptide, using extensive, unbiased molecular dynamics simulations. The results provide clear evidence for turn-directed broken-zipper folding and reveal details of turn nucleation and cooperative progression of turn growth, hydrogen-bond formations, and eventual packing of the hydrophobic core. Further, we show that, rather than driving folding through hydrophobic collapse, cross-strand side-chain packing could in fact be rate-limiting as packing frustrations can delay formation of the native hydrophobic core prior to or during folding and even cause relatively long-living misfolded or partially folded states that may nucleate aggregative events in more complex situations. The results support the increasing evidence for turn-centric folding mechanisms for β-hairpin formation suggested recently for GB1 and Peptide 1 based on experiments and simulations but also point to the need for similar examinations of polypeptides with larger numbers of cross-strand hydrophobic residues. 相似文献
993.
Gören AC Akçicek E Dirmenci T Kilic T Mozioğlu E Yilmaz H 《Natural product research》2012,26(1):84-90
The fatty acid composition of the seed oil of 23 Stachys taxa was analysed by GC/MS. The main compounds were found to be linoleic (27.1-64.3%), oleic (20.25-48.1%), palmitic (4.3-9.1%), stearic (trace to 5.2%) and 6-octadecynoic (2.2-34.1%) acids. The latter compound could be used as a chemotaxonomic marker of the genus Stachys. A cluster analysis was performed for comparison and characterisation of the seed oil from Stachys species. 相似文献
994.
Microwave heating in solid-phase peptide synthesis 总被引:1,自引:0,他引:1
The highly refined organic chemistry in solid-phase synthesis has made it the method of choice not only to assemble peptides but also small proteins - mainly on a laboratory scale but increasingly also on an industrial scale. While conductive heating occasionally has been applied to peptide synthesis, precise microwave irradiation to heat the reaction mixture during coupling and N(α)-deprotection has become increasingly popular. It has often provided dramatic reductions in synthesis times, accompanied by an increase in the crude peptide purity. Microwave heating has been proven especially relevant for sequences which might form β-sheet type structures and for sterically difficult couplings. The beneficial effect of microwave heating appears so far to be due to the precise nature of this type of heating, rather than a peptide-specific microwave effect. However, microwave heating as such is not a panacea for all difficulties in peptide syntheses and the conditions may need to be adjusted for the incorporation of Cys, His and Asp in peptides, and for the synthesis of, for example, phosphopeptides, glycopeptides, and N-methylated peptides. Here we provide a comprehensive overview of the advances in microwave heating for peptide synthesis, with a focus on systematic studies and general protocols, as well as important applications. The assembly of β-peptides, peptoids and pseudopeptides are also evaluated in this critical review (254 references). 相似文献
995.
Dr. Andrea Bernardos Dr. Laura Mondragón Dr. Irakli Javakhishvili Núria Mas Cristina de la Torre Prof. Ramón Martínez‐Máñez Dr. Félix Sancenón Prof. José M. Barat Prof. Søren Hvilsted Dr. Mar Orzaez Dr. Enríque Pérez‐Payá Prof. Pedro Amorós 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(41):13068-13078
The synthesis and characterisation of new capped silica mesoporous nanoparticles for on‐command delivery applications is reported. Functional capped hybrid systems consist of MCM‐41 nanoparticles functionalised on the external surface with polyesters bearing azobenzene derivatives and rhodamine B inside the mesopores. Two solid materials, Rh‐PAzo8‐S and Rh‐PAzo6‐S, containing two closely related polymers, PAzo8 and PAzo6, in the pore outlets have been prepared. Materials Rh‐PAzo8‐S and Rh‐PAzo6‐S showed an almost zero release in water due to steric hindrance imposed by the presence of anchored bulky polyesters, whereas a large delivery of the cargo was observed in the presence of an esterase enzyme due to the progressive hydrolysis of polyester chains. Moreover, nanoparticles Rh‐PAzo8‐S and Rh‐PAzo6‐S were used to study the controlled release of the dye in intracellular media. Nanoparticles were not toxic for HeLa cells and endocytosis‐mediated cell internalisation was confirmed by confocal microscopy. Furthermore, the possible use of capped materials as a drug‐delivery system was demonstrated by the preparation of a new mesoporous silica nanoparticle functionalised with PAzo6 and loaded with the cytotoxic drug camptothecin (CPT‐PAzo6‐S). Following cell internalisation and lysosome resident enzyme‐dependent gate opening, CPT‐PAzo6‐S induced CPT‐dependent cell death in HeLa cells. 相似文献
996.
Wei Wei Yu‐jie Fu Yuan‐gang Zu Wei Wang Meng Luo Chun‐jian Zhao Chun‐ying Li Lin Zhang Zuo‐fu Wei 《Journal of separation science》2012,35(21):2875-2883
In this study, an ionic liquid‐based microwave‐assisted extraction (ILMAE) followed by high‐performance liquid chromatograph y ‐diode array detector with a pentafluorophenyl column for the extraction and quantification of eight flavonoid glycosides in pigeon pea leaves is described. Compared with conventional extraction methods, ILMAE is a more effective and environment friendly method for the extraction of nature compounds from herbal plants. Nine different types of ionic liquids with different cations and anions were investigated. The results suggested that varying the anion and cation had significant effects on the extraction of flavonoid glycosides, and 1.0 M 1‐butyl‐3‐methylimidazolium bromide ([C4MIM]Br) solution was selected as solvent. In addition, the extraction procedures were also optimized using a series of single‐factor experiments. The optimum parameters were obtained as follows: extraction temperature 60°C, liquid–solid ratio 20:1 mL/g and extraction time 13 min. Moreover, an HPLC method using pentafluorophenyl column was established and validated. Good linearity was observed with the regression coefficients (r2) more than 0.999. The limit of detection (LODs) (S/N = 3) and limit of quantification (LOQs) (S/N = 10) for the components were less than 0.41 and 1.47 μg/mL, respectively. The inter‐ and intraday precisions that were used to evaluate the reproducibility and relative standard deviation (RSD) values were less than 4.57%. The recoveries were between 97.26 and 102.69%. The method was successfully used for the analysis of samples of pigeon pea leaves. In conclusion, the developed ILMAE‐HPLC‐diode array detector using pentafluorophenyl column method can be applied for quality control of pigeon pea leaves and related medicinal products. 相似文献
997.
Kleiman-Shwarsctein A Laursen AB Cavalca F Tang W Dahl S Chorkendorff I 《Chemical communications (Cambridge, England)》2012,48(7):967-969
A novel method for the deposition of RuO(2) from RuO(4)(g) on diverse metal oxides has been developed by grafting dopamine onto the otherwise un-reactive metal oxide surface. Oxygen evolution reaction on TiO(2) and the photoelectrochemical improvement of WO(3) by deposition of RuO(2) are just a few examples where this novel deposition method can be used. 相似文献
998.
Fatty acid compositions of seeds of five taxa of the Juniperus section of the genus Juniperus L. (Cupressaceae), i. e. J. drupacea Lab., J. communis L. var. communis, J. communis var. saxatilis Pall., J. oxycedrus L. subsp. oxycedrus, and J. oxycedrus subsp. macrocarpa (Sibth. & Sm.) Ball, were investigated. Methyl ester derivatized fatty acids of the lipophylic extracts of the five species were comparatively analyzed by capillary gas chromatography-mass spectrometry (GC-MS). Juniperus taxa showed uniform fatty acid patterns, among which linoleic (25.8 - 32.5%), pinolenic (11.9 - 24.1%) and oleic acids (12.4 - 17.2%) were determined to be the main fractions in the seed oils. Juniperonic acid was found to be remarkably high in J. communis var. saxatilis (11.4%), J. oxycedrus subsp. oxycedrus (10.4%), and J. communis var. communis (10.1%). To the best of our knowledge, the present work discloses the first report on the fatty acid compositions of seeds of this Juniperus section grown in Turkey. 相似文献
999.
Moskun AC Bradforth SE Thøgersen J Keiding S 《The journal of physical chemistry. A》2006,110(38):10947-10955
Ultrafast pump-broadband probe spectroscopy was used to study the transient photoproducts following 200-nm photodetachment of I(-)(aq). Resonant detachment at 200 nm in the second charge-transfer-to-solvent (CTTS) band of I(-)(aq) is expected to produce an electron and iodine in its spin-orbit excited state, I*((2)P(1/2)). The transients in solution following photodetachment were probed from 200 to 620 nm. Along with strong absorption in the visible region due to solvated electrons and a strong bleach of the I(-)(aq) ground-state absorption, a weaker transient absorption near 260 nm was observed that is consistent with a previously assigned ground-state I((2)P(3/2)) charge-transfer band. However, no evidence was found for an equivalent I*(aq) charge-transfer absorption, and I((2)P(3/2)) was produced within the instrument response. This suggests either that I* is electronically relaxed in less than 300 fs or that excitation in the second CTTS band does not in fact lead to I*. The consequences for previous experimental work where I*(aq) production has been postulated, as well as for halogen electron ejection mechanisms, are discussed. In addition, the broad spectral coverage of this study reveals in the bleach recovery the rapid cooling of the solvent surrounding the re-formed iodide after geminate recombination of the iodine with the solvated electron. 相似文献
1000.
Effects of surface area, free volume, and heat of adsorption on hydrogen uptake in metal-organic frameworks 总被引:1,自引:0,他引:1
Grand canonical Monte Carlo simulations were performed to predict adsorption isotherms for hydrogen in a series of 10 isoreticular metal-organic frameworks (IRMOFs). The results show acceptable agreement with the limited experimental results from the literature. The effects of surface area, free volume, and heat of adsorption on hydrogen uptake were investigated by performing simulations over a wide range of pressures on this set of materials, which all have the same framework topology and surface chemistry but varying pore sizes. The results reveal the existence of three adsorption regimes: at low pressure (loading), hydrogen uptake correlates with the heat of adsorption; at intermediate pressure, uptake correlates with the surface area; and at the highest pressures, uptake correlates with the free volume. The accessible surface area and free volume, calculated from the crystal structures, were also used to estimate the potential of these materials to meet gravimetric and volumetric targets for hydrogen storage in IRMOFs. 相似文献