全文获取类型
收费全文 | 626篇 |
免费 | 32篇 |
国内免费 | 1篇 |
专业分类
化学 | 388篇 |
晶体学 | 1篇 |
力学 | 31篇 |
数学 | 44篇 |
物理学 | 195篇 |
出版年
2023年 | 10篇 |
2022年 | 8篇 |
2021年 | 10篇 |
2020年 | 21篇 |
2019年 | 21篇 |
2018年 | 19篇 |
2017年 | 11篇 |
2016年 | 29篇 |
2015年 | 23篇 |
2014年 | 29篇 |
2013年 | 72篇 |
2012年 | 61篇 |
2011年 | 49篇 |
2010年 | 33篇 |
2009年 | 28篇 |
2008年 | 33篇 |
2007年 | 43篇 |
2006年 | 28篇 |
2005年 | 26篇 |
2004年 | 7篇 |
2003年 | 12篇 |
2002年 | 9篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1998年 | 3篇 |
1997年 | 5篇 |
1996年 | 2篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1992年 | 5篇 |
1991年 | 1篇 |
1990年 | 3篇 |
1989年 | 2篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 5篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1982年 | 5篇 |
1981年 | 6篇 |
1980年 | 4篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1977年 | 3篇 |
1976年 | 2篇 |
1973年 | 1篇 |
1966年 | 1篇 |
1963年 | 1篇 |
1939年 | 1篇 |
排序方式: 共有659条查询结果,搜索用时 203 毫秒
61.
Om Prakash Shiv Kumar Pushkar Singh Volker Deckert S. Chatterjee A.K. Ghosh Ranjan K. Singh 《Journal of Raman spectroscopy : JRS》2016,47(7):813-818
Interest in the synthesis of hybrid substrates for surface‐enhanced Raman scattering (SERS) has surged recently. Hereof, in the present work, a hybrid SERS substrate CuO : Mn/Ag heterojunction has been synthesised. To accomplish this, the nanostructred Ag island film and CuO : Mn nanoparticles are synthesised by vacuum thermal evaporation method and sol–gel method respectively, and thereafter, a heterojunction between the CuO : Mn and Ag is fabricated by adsorption of CuO : Mn (10‐3 m in ethanol) on Ag island film. Further, the SERS sensitivity of CuO : Mn/Ag heterojunctions has been studied by probing methyl orange. We observed that with Mn‐doping in the lattice of CuO, the SERS signal is enhanced considerably because of ferromagnetic ordering in CuO : Mn. DFT/B3LYP/6‐311 G(d, p) method is used to calculate the energy of HOMO and LUMO level of methyl orange. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
62.
Zofia M. Wosinska Faye L. Stump Rajeev Ranjan Edward D. Lorance GeNita N. Finley Priya P. Patel Muzamil A. Khawaja Katie L. Odom Wolfgang H. Kramer Ian R. Gould 《Photochemistry and photobiology》2014,90(2):313-328
Irreversible photooxidation based on N–O bond fragmentation is demonstrated for N‐methoxyheterocycles in both the singlet and triplet excited state manifolds. The energetic requirements for bond fragmentation are studied in detail. Bond fragmentation in the excited singlet manifold is possible for ππ* singlet states with energies significantly larger than the N–O bond dissociation energy of ca 55 kcal mol?1. For the nπ* triplet states, N–O bond fragmentation does not occur in the excited state for orbital overlap and energetic reasons. Irreversible photooxidation occurs in the singlet states by bond fragmentation followed by electron transfer. Irreversible photooxidation occurs in the triplet states via bimolecular electron transfer to the donor followed by bond fragmentation. Using these two sensitization schemes, donors can be irreversibly oxidized with oxidation potentials ranging from ca 1.6–2.2 V vs SCE. The corresponding N‐ethylheterocycles are characterized as conventional reversible photooxidants in their triplet states. The utility of these sensitizers is demonstrated by irreversibly generating the guanosine radical cation in buffered aqueous solution. 相似文献
63.
We have studied the valence and electronic properties of Mn doped SrRuO3 using electrical transport measurement, X-ray photoelectron spectroscopy (XPS) and local (spin) density approximation plus Coulomb interaction strength calculation (LSDA+U). The resistivity data revealed that the system undergoes transition from metal to insulator at the critical Mn doping level, x∼0.2, which is accompanied by the structural transition from orthorhombic to tetragonal crystal symmetry. Besides, the significant reduction of the spectral weight at the coherent zone (0.8 eV) of the valence band is observed for x>0.2. The core XPS spectra suggest that both the transition elements exist in the mixed ionic pair, Ru+4/Ru+5↔Mn+3/Mn+4. The detail analysis of the results suggests that the Coulomb correlation effect in conjugation with localization of the charge carriers predominate over the mixed ionic pair effect and responsible for the metal-insulator transition in the series. 相似文献
64.
A three-component coupling of vinyl triflates and boronic acids to alkenes catalyzed by palladium is reported. Using 1,3-dienes, selective 1,2-alkene difunction-alization is observed, whereas the use of terminal alkenes results in 1,1-alkene difunctionalization. The reaction outcome is attributed to the formation of stabilized, cationic Pd-π-allyl intermediates to regulate β-hydride elimination. 相似文献
65.
Wang J Lu H Kamat R Pingali SV Urban VS Cheng J Lin Y 《Journal of the American Chemical Society》2011,133(33):12906-12909
The helical and tubular structures self-assembled from proteins have inspired scientists to design synthetic building blocks that can be "polymerized" into supramolecular polymers through coordinated noncovalent interactions. However, cooperative supramolecular polymerization from large, synthetic macromolecules remains a challenge because of the difficulty of controlling the structure and interactions of macromolecular monomers. Herein we report the synthesis of polypeptide-grafted comb polymers and the use of their tunable secondary interactions in solution to achieve controlled supramolecular polymerization. The resulting tubular supramolecular structures, with external diameters of hundreds of nanometers and lengths of tens of micrometers, are stable and resemble to some extent biological superstructures assembled from proteins. This study shows that highly specific intermolecular interactions between macromolecular monomers can enable the cooperative growth of supramolecular polymers. The general applicability of this strategy was demonstrated by carrying out supramolecular polymerization from gold nanoparticles grafted with the same polypeptides on the surface. 相似文献
66.
Ren Y Paira P Nayak TR Ang WH Pastorin G 《Chemical communications (Cambridge, England)》2011,47(27):7710-7712
A "direct encapsulation" method was developed for the synthesis of highly stable water-soluble fullerene@gold core-shell nanostructures, with gold nanoshells showing either closed or porous morphology. This gold nano-shell coating formed a "nano-oven", capable of decomposing encapsulated fullerene molecules rapidly when irradiated by laser. We envisaged this being a useful tool for chemical reactions as well as a novel scaffold for nano-material synthesis. 相似文献
67.
Jena BK Sahu SC Satpati B Sahu RK Behera D Mohanty S 《Chemical communications (Cambridge, England)》2011,47(13):3796-3798
A facile approach has been developed for synthesis of highly-structured, anisotropic Pd nanostructures. The dendritic Pd nanostructures show superior performance toward oxidation of formic acid and methanol for fuel cell application. 相似文献
68.
69.
2-Aminopyridinium maleate (2APM) is a recently discovered organic acid-base complex that crystallizes in a non-centrosymmetric space group Pc and hence has a nonzero second-order optical susceptibility. In 2APM the cation (aminopyridinium ion) is connected to the anion (maleate ion) through hydrogen bonds (N1-H10–O2 and N2-H12–O1), we have calculated the molecular properties of 2APM for varying strength of these hydrogen bonds. It is observed that the molecular hyperpolarizabilty varies for varying strength of these hydrogen bonds. These observations are interpreted in terms of the change in nature of the hydrogen bond interaction as its strength is varied. Macropscopic second-order optical susceptibility (d 0) of 2APM is obtained using the calculated value of molecular hyperpolarizability and the reported crystal structure of 2APM. In order to study the influence of molecular packing on the macroscopic non-linear optical property of the crystal, susceptibility calculations are repeated for 2-methyl-4nitroaniline (MNA) crystal, which is a very well known non-linear optical organic crystal with an exceptionally high value of second-order optical susceptibility. A comparison between the non-linear optical property of 2APM and MNA crystals is given. Comparing the values of d 0 of 2APM crystals with that of urea shows that the nonlinear optical response of 2APM crystals will be nearly 10 times that of a urea crystal. 相似文献
70.
G. Ranga Rao H. Ranjan Sahu Braja Gopal Mishra 《Colloids and surfaces. A, Physicochemical and engineering aspects》2003,220(1-3):261-269
Surface and catalytic properties of Cu–Ce–O composite materials prepared by solution combustion method have been investigated. The materials are characterized by X-ray diffraction (XRD), temperature programmed reduction (TPR) and electron paramagnetic resonance spectroscopy (EPR). The results of EPR and TPR show finely dispersed Cu2+ species on ceria matrix with low copper content. The Cu2+ species exists in the form of dimers and clusters which are not evident in XRD. In addition CuO is also present as small clusters which grow to larger size at higher Cu content. There is no evidence of CuO forming a solid solution with fluorite CeO2 in combustion method. The Cu2+ species mostly appear on surface rather than in the bulk. Hydrogen peroxide decomposition kinetics has been carried out on Cu–Ce–O composite materials to investigate the effect of crystalline and well-dispersed copper oxide phases on CeO2. From kinetic results, the catalyst materials can be grouped into highly dispersed as well as crystalline CuO phases present on CeO2 matrix. Two parallel compensating lines for dispersed and crystalline CuO phases on CeO2 are observed in ln A versus Ea plot indicating the compensation effect in H2O2 decomposition. This observation is consistent with XRD and EPR results. 相似文献