全文获取类型
收费全文 | 286篇 |
免费 | 8篇 |
专业分类
化学 | 247篇 |
晶体学 | 1篇 |
力学 | 1篇 |
数学 | 5篇 |
物理学 | 40篇 |
出版年
2023年 | 3篇 |
2022年 | 1篇 |
2021年 | 6篇 |
2020年 | 3篇 |
2019年 | 2篇 |
2018年 | 2篇 |
2016年 | 5篇 |
2015年 | 3篇 |
2014年 | 3篇 |
2013年 | 12篇 |
2012年 | 24篇 |
2011年 | 15篇 |
2010年 | 12篇 |
2009年 | 5篇 |
2008年 | 17篇 |
2007年 | 23篇 |
2006年 | 25篇 |
2005年 | 17篇 |
2004年 | 18篇 |
2003年 | 8篇 |
2002年 | 11篇 |
2001年 | 7篇 |
2000年 | 5篇 |
1999年 | 8篇 |
1998年 | 2篇 |
1997年 | 4篇 |
1996年 | 6篇 |
1995年 | 2篇 |
1994年 | 1篇 |
1993年 | 7篇 |
1992年 | 1篇 |
1991年 | 4篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1988年 | 4篇 |
1987年 | 1篇 |
1985年 | 1篇 |
1984年 | 4篇 |
1983年 | 1篇 |
1981年 | 5篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1977年 | 2篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1970年 | 2篇 |
1968年 | 1篇 |
排序方式: 共有294条查询结果,搜索用时 78 毫秒
21.
Dynarowicz-L&acedil;tka P Kita K Milart P Dhanabalan A Cavalli A Oliveira ON 《Journal of colloid and interface science》2001,239(1):145-157
A series of 5'-phenyl-m-terphenyl carboxylic acid (PTCA) derivatives with methyl, chloro, and fluoro substituents at both side phenyl rings have been synthesized and characterized as Langmuir monolayers at the air/water interface. A comparative analysis, based on the surface pressure and electric surface potential measurements under a variety of experimental conditions, is complemented with BAM images. Copyright 2001 Academic Press. 相似文献
22.
M. Bonesini E. Bonvin R. Bopp L. J. Carroll A. J. Cass D. Cavalli G. Costa S. U. Chung M. Donnat P. A. Dorsaz M. Feliks J. R. Fischer L. Fluri F. Gianotti S. Jack J. N. Jackson M. N. Kienzle-Focacci J. G. Lynch L. Mandelli M. Martin L. Mathys A. Maxwell M. Mazzanti P. J. Negus S. Pensotti-Rancoita L. Perini D. Perrin R. W. Poultney W. H. Range L. Rosselet S. W. Snow A. S. Thompson R. M. Turnbull J. Wells M. Werlen WA Collaboration 《Zeitschrift fur Physik C Particles and Fields》1989,44(1):71-78
The structure of events associated with the production of direct photons in π? p, π+ p andpp reactions of 280 GeV/c has been studied using data from the WA 70 experiment at the CERN SPS. Results are presented on the distributions of the fractional momenta of the colliding partons and on the fragmentation of the recoil jet and a comparison is made with predictions using the structure functions of Duke and Owens in the Lund Monte Carlo with string fragmentation. 相似文献
23.
The hydration of the phosphocholine headgroup in 1,2-dipropionyl-sn-glycero-3-phosphocholine (C(3)-PC) in solution has been determined by using neutron diffraction enhanced with isotopic substitution in combination with computer simulation techniques. The atomic scale hydration structure around this head group shows that both the -N(CH(3))(3) and -CH(2) portions of the choline headgroup are strongly associated with water, through a unique hydrogen bonding regime, where specifically a hydrogen bond from the C-H group to water and a strong association between the water oxygen and N(+) atom in solution have both been observed. In addition, both PO(4) oxygens (P=O) and C=O oxygens are oversaturated when compared to bulk water in that the average number of hydrogen bonds from water to both X=O oxygens is about 2.5 for each group. That water binds strongly to the glycerol groups and is suggestive that water may bind to these groups when phosophotidylcholine is embedded in a membrane bilayer. 相似文献
24.
Dr. Daniele Fazzi Dr. Eleonora V. Canesi Prof. Fabrizia Negri Dr. Chiara Bertarelli Prof. Chiara Castiglioni 《Chemphyschem》2010,11(17):3685-3695
The quinoidal versus biradicaloid character of the ground state of a series of thiophene‐based heterophenoquinones is investigated with quantum‐chemical calculations. The role of the ground‐state electronic character on molecular structure and vibrational properties is emphasized. The vibrational activities are experimentally determined and their analysis is performed by taking advantage of the definition of a collective vibrational coordinate (the
25.
X-band (9.60 GHz) electron paramagnetic resonance (EPR) spectra of the Er3+ Kramers ion substituting for the Y3+ ion in yttrium vanadate (YVO4) single crystal were recorded at liquid-helium temperatures. Fine and hyperfine EPR transitions were observed for the 166Er (zero nuclear magnetic moment) and 167Er (I=7/2) isotopes, respectively. The values of the elements of the anisotropic
2- and Ã2-tensors of the 167Er3+ ion, and those of the
2 tensor for the 166Er ion, were estimated. The admixture of crystal-field wave functions in the ground-state wave function of Er3+ were determined using the experimental g-values. 相似文献
26.
Roberta Cavalli Emilio Marengo Otto Caputo Elena Ugazio Maria Rosa Gasco 《Journal of Dispersion Science and Technology》2013,34(7):717-734
The influence of twenty five different alcohols on the formation of warm oil-in-water (O/W) microemulsions was investigated. Selected concentrations of each alcohol were added to fixed amounts of stearic acid, Tween 20 and water at 65 ° C. Fifteen alcohols formed microemulsions, at least at one of the concentrations. A pattern recognition study was performed to elucidate the activities of the alcohols by Principal Component Analysis (PCA). Linear Discriminant Analysis (LDA) was used to classify them. Two classification functions, obtained for alcohols forming / not forming microemulsions, suggest that the formation of warm O/W microemulsion is linked to the nature and the dimension/lipophilicity of the alcohol. 相似文献
27.
Multitarget Drug Discovery for Alzheimer's Disease: Triazinones as BACE‐1 and GSK‐3β Inhibitors 下载免费PDF全文
Federica Prati Dr. Angela De Simone Dr. Paola Bisignano Dr. Andrea Armirotti Dr. Maria Summa Dr. Daniela Pizzirani Dr. Rita Scarpelli Dr. Daniel I. Perez Prof. Dr. Vincenza Andrisano Dr. Ana Perez‐Castillo Prof. Dr. Barbara Monti Francesca Massenzio Dr. Letizia Polito Prof. Dr. Marco Racchi Dr. Angelo D. Favia Dr. Giovanni Bottegoni Prof. Dr. Ana Martinez Prof. Dr. Maria Laura Bolognesi Prof. Dr. Andrea Cavalli 《Angewandte Chemie (International ed. in English)》2015,54(5):1578-1582
Cumulative evidence strongly supports that the amyloid and tau hypotheses are not mutually exclusive, but concomitantly contribute to neurodegeneration in Alzheimer′s disease (AD). Thus, the development of multitarget drugs which are involved in both pathways might represent a promising therapeutic strategy. Accordingly, reported here in is the discovery of 6‐amino‐4‐phenyl‐3,4‐dihydro‐1,3,5‐triazin‐2(1H)‐ones as the first class of molecules able to simultaneously modulate BACE‐1 and GSK‐3β. Notably, one triazinone showed well‐balanced in vitro potencies against the two enzymes (IC50 of (18.03±0.01) μM and (14.67±0.78) μM for BACE‐1 and GSK‐3β, respectively). In cell‐based assays, it displayed effective neuroprotective and neurogenic activities and no neurotoxicity. It also showed good brain permeability in a preliminary pharmacokinetic assessment in mice. Overall, triazinones might represent a promising starting point towards high quality lead compounds with an AD‐modifying potential. 相似文献
28.
Collini D De Biani FF Dolzhnikov DS Femoni C Iapalucci MC Longoni G Tiozzo C Zacchini S Zanello P 《Inorganic chemistry》2011,50(7):2790-2798
The previously ill-characterized [H(x)Rh(22)(CO)(35)](4-/5-) carbonyl cluster has been obtained as a byproduct of the synthesis of [H(3)Rh(13)(CO)(24)](2-) and effectively separated by metathesis of their sodium salts with [NEt(4)]Cl. Although the yields are modest and never exceed 10-15% (based on Rh), this procedure affords spectroscopically pure [H(3)Rh(22)(CO)(35)](5-) anion. Formation of the latter in mixture with other Rh clusters was also observed by electrospray ionization-mass spectrometry (ESI-MS) in the oxidation of [H(2)Rh(13)(CO)(24)](3-) with Cu(2+) salts. The recovery of further amounts of [H(3)Rh(22)(CO)(35)](5-) was hampered by too similar solubility of the salts composing the mixture. Conversely, the reaction in CH(3)CN of [H(2)Rh(13)(CO)(24)](3-) with [Cu(MeCN)(4)](+)[BF(4)](-) leads to the [H(2)Rh(13)(CO)(24){Cu(MeCN)}(2)](-) bimetallic cluster. The X-ray crystal structures of [H(4)Rh(22)(CO)(35)](4-), [H(3)Rh(22)(CO)(35)](5-), and [H(2)Rh(13)(CO)(24){Cu(MeCN)}(2)](-) are reported. From a formal point of view, the metal frame of the former two species can be derived by interpenetration along two orthogonal axes of two moieties displaying the structure of the latter. The availability of [H(8-n)Rh(22)(CO)(35)](n-) salts prompted their detailed chemical, spectroscopic, and electrochemical characterization. The presence of hydride atoms has been directly proved both by ESI-MS and (1)H NMR. Moreover, both [H(4)Rh(22)(CO)(35)](4-) and [H(3)Rh(22)(CO)(35)](5-) undergo distinctive electrochemically reversible redox changes. This allows to assess electrochemical studies as indisputable though circumstantial evidence of the presence of (1)H NMR-silent hydride atoms in isostructural anions of different charge. 相似文献
29.
De Fazio D Lucas JM Aquilanti V Cavalli S 《Physical chemistry chemical physics : PCCP》2011,13(18):8571-8582
Exact quantum reactive scattering calculations in the collision energy range 1-250 meV have been carried out for both the isotopic product channels of the title system. The dynamical studies compares an ab initio potential energy surface (PES) recently appeared in the literature (J. Chem. Phys., 2008, 129, 011103) with other phenomenological PESs. Vibrational branching ratios, cross sections and rate constants are presented and compared with molecular beam scattering experiments as well as with chemical kinetics data. In particular, the agreement of the vibrational branching ratios with experimental measurements is improved with respect to previous studies on other PESs, mainly because of the presence of a broad peak in the HF(v' = 3) integral cross section completely absent in the previous simulations. This feature, observed by molecular beam experiments, is the fingerprint of a new reaction mechanism operative in the dynamics described by the new PES. A conjecture for its origin, able to explain many of its characteristic aspects, is analyzed and discussed. 相似文献