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排序方式: 共有138条查询结果,搜索用时 734 毫秒
131.
Beckmann T Linnenbank H Steigerwald H Sturman B Haertle D Buse K Breunig I 《Physical review letters》2011,106(14):143903
Whispering-gallery resonators (WGR's), based on total internal reflection, possess high quality factors in a broad spectral range. Thus, nonlinear-optical processes in such cavities are ideally suited for the generation of broadband or tunable electromagnetic radiation. Experimentally and theoretically, we investigate the tunability of optical parametric oscillation in a radially structured WGR made of lithium niobate. With a 1.04 μm pump wave, the signal and idler waves are tuned from 1.78 to 2.5 μm--including the point of degeneracy--by varying the temperature between 20 and 62?°C. A weak off centering of the radial domain structure extends considerably the tuning capabilities. The oscillation threshold lies in the mW-power range. 相似文献
132.
Manganese(IV)‐Mediated Hydroperoxyarylation of Alkenes with Aryl Hydrazines and Dioxygen from Air
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Stephanie Kindt Dr. Hannelore Jasch Prof. Dr. Markus R. Heinrich 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(21):6251-6255
We report a new carbooxygenation‐type version of the Meerwein arylation in which the introduction of oxygen is achieved by using dioxygen from the air. In this way, hydroperoxides were obtained from activated as well as non‐activated alkenes by oxidizing aryl hydrazines with manganese dioxide. The best results were obtained with α‐substituted acrylates. Importantly, the aryl hydrazine has to be added slowly to the reaction mixture to allow sufficient uptake of dioxygen from the air. Competition and labeling experiments revealed hydroperoxyl radicals as novel oxygen‐centered radical scavengers. 相似文献
133.
Synthesis and Characterization of Organic Dyes with Various Electron‐Accepting Substituents for p‐Type Dye‐Sensitized Solar Cells
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Martin Weidelener Dr. Satvasheel Powar Hannelore Kast Dr. Ze Yu Dr. Pablo P. Boix Dr. Chen Li Prof. Klaus Müllen Dr. Thomas Geiger Dr. Simon Kuster Prof. Frank Nüesch Prof. Udo Bach Dr. Amaresh Mishra Prof. Peter Bäuerle 《化学:亚洲杂志》2014,9(11):3251-3263
Four new donor‐π‐acceptor dyes differing in their acceptor group have been synthesized and employed as model systems to study the influence of the acceptor groups on the photophysical properties and in NiO‐based p‐type dye‐sensitized solar cells. UV/Vis absorption spectra showed a broad range of absorption coverage with maxima between 331 and 653 nm. Redox potentials as well as HOMO and LUMO energies of the dyes were determined from cyclic voltammetry measurements and evaluated concerning their potential use as sensitizers in p‐type dye‐sensitized solar cells (p‐DSCs). Quantum‐chemical density functional theory calculations gave further insight into the frontier orbital distributions, which are relevant for the electronic processes in p‐DSCs. In p‐DSCs using an iodide/triiodide‐based electrolyte, the polycyclic 9,10‐dicyano‐acenaphtho[1,2‐b]quinoxaline (DCANQ) acceptor‐containing dye gave the highest power conversion efficiency of 0.08 %, which is comparable to that obtained with the perylenemonoimide (PMI)‐containing dye. Interestingly, devices containing the DCANQ‐based dye achieve a higher VOC of 163 mV compared to 158 mV for the PMI‐containing dye. The result was further confirmed by impedance spectroscopic analysis showing higher recombination resistance and thus a lower recombination rate for devices containing the DCANQ dye than for PMI dye‐based devices. However, the use of the strong electron‐accepting tricyanofurane (TCF) group played a negative role in the device performance, yielding an efficiency of only 0.01 % due to a low‐lying LUMO energy level, thus resulting in an insufficient driving force for efficient dye regeneration. The results demonstrate that a careful molecular design with a proper choice of the acceptor unit is essential for development of sensitizers for p‐DSCs. 相似文献
134.
Zhang J Hughes TF Steigerwald M Brus L Friesner RA 《Journal of the American Chemical Society》2012,134(29):12028-12042
We have developed a cluster model of a TiO(2) nanoparticle in the dye-sensitized solar cell and used first-principles quantum chemistry, coupled with a continuum solvation model, to compute structures and energetics of key electronic and structural intermediates and transition states. Our results suggest the existence of shallow surface trapping states induced by small cations and continuum solvent effect as well as the possibility of the existence of a surface band which is 0.3-0.5 eV below the conduction band edge. The results are in uniformly good agreement with experiment and establish the plausibility of an ambipolar model of electron diffusion in which small cations, such as Li(+), diffuse alongside the current carrying electrons in the device, stabilizing shallowing trapping states, facilitating diffusion from one of these states to another, in a fashion that is essential to the functioning of the cell. 相似文献
135.
Klausen RS Widawsky JR Steigerwald ML Venkataraman L Nuckolls C 《Journal of the American Chemical Society》2012,134(10):4541-4544
Bulk silicon, the bedrock of information technology, consists of the deceptively simple electronic structure of just Si-Si σ bonds. Diamond has the same lattice structure as silicon, yet the two materials have dramatically different electronic properties. Here we report the specific synthesis and electrical characterization of a class of molecules, oligosilanes, that contain strongly interacting Si-Si σ bonds, the essential components of the bulk semiconductor. We used the scanning tunneling microscope-based break-junction technique to compare the single-molecule conductance of these oligosilanes to those of alkanes. We found that the molecular conductance decreases exponentially with increasing chain length with a decay constant β = 0.27 ± 0.01 ?(-1), comparable to that of a conjugated chain of C═C π bonds. This result demonstrates the profound implications of σ conjugation for the conductivity of silicon. 相似文献
136.
Stanković S Goossens H Catak S Tezcan M Waroquier M Van Speybroeck V D'hooghe M De Kimpe N 《The Journal of organic chemistry》2012,77(7):3181-3190
The reactivity of 2-bromomethyl-2-methylaziridines toward oxygen, sulfur, and carbon nucleophiles in different solvent systems was investigated. Remarkably, the choice of the solvent has a profound influence on the reaction outcome, enabling the selective formation of either functionalized aziridines in dimethylformamide (through direct bromide displacement) or azetidines in acetonitrile (through rearrangement via a bicyclic aziridinium intermediate). In addition, the experimentally observed solvent-dependent behavior of 2-bromomethyl-2-methylaziridines was further supported by means of DFT calculations. 相似文献
137.
Xiao S Tang J Beetz T Guo X Tremblay N Siegrist T Zhu Y Steigerwald M Nuckolls C 《Journal of the American Chemical Society》2006,128(33):10700-10701
This study details a new derivative of the contorted HBCs that self-organizes into one-dimensional, single-crystalline fibers. X-ray diffraction, transmission electron microscopy, and electron diffraction studies show that they have an orthorhombic unit cell with dimensions of 5.8 nm x 4.5 nm x 0.45 nm. Each fiber is composed of a few thousands columns. A method is put forth that utilizes elastomer stamps to manipulate and position isolated fibers in organic field effect transistors. 相似文献
138.
Amino acids are important targets for metabolic profiling. For decades, amino acid analysis has been accomplished by either
cation-exchange or reversed-phase liquid chromatography coupled to UV absorbance or fluorescence detection of pre-column or
post-column-derivatized amino acids. Recent years have seen great progress in the development of direct-infusion or hyphenated
mass spectrometry in the analysis of free amino acids in physiological fluids, because mass spectrometry not only matches
optical detection in sensitivity, but also offers superior selectivity. The advent of cryo-probes has also brought NMR spectroscopy
within the detection limits required for the analysis of free amino acids. But there is still room for further improvement,
including expansion of the analyte spectrum, reduction of sample preparation and analysis time, automation, and synthesis
of affordable isotope standards.
Figure Fully automated gas chromatography-mass spectrometry analysis of amino acids. 相似文献