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排序方式: 共有441条查询结果,搜索用时 31 毫秒
1.
W. Bamogo L. Mugherli A. Banyasz A. Novelli-Rousseau F. Mallard T.-H. Tran-Thi 《Analytica chimica acta》2015
A detection method for nicotinic acid, a specific metabolite marker of Mycobacterium tuberculosis present in cultures and patients' breath, is studied in complex solutions containing other metabolites and in biological media such as urine, saliva and breath condensate. The method is based on the analysis of the luminescence increase of Tb3+ complexes in the presence of nicotinic acid due to the energy transfer from the excited ligand to the lanthanide ion. It is shown that other potential markers found in M. tuberculosis culture supernatant, such as methyl phenylacetate, p-methyl anisate, methyl nicotinate and 2-methoxy biphenyl, can interfere with nicotinic acid via a competitive absorption of the excitation photons. A new strategy to circumvent these interferences is proposed with an upstream trapping of volatile markers preceding the detection of nicotinic acid in the liquid phase via the luminescence of Tb3+ complexes. The cost of the method is evaluated and compared with the Xpert MTB/RIF test endorsed by the World Health Organization. 相似文献
2.
《Comptes Rendus Chimie》2017,20(3):230-236
Long-range electron transfer reactions play a key role in biological photosynthesis, and they are likely to play an important role for future artificial photosynthetic endeavors as well. The possibility to control the rates for long-range electron transfer with external stimuli is of particular interest in this context. In the work presented herein, we explored a donor–bridge–acceptor compound in which intramolecular electron transfer from a triarylamine donor to a photoexcited Ru(bpy)32+ (bpy = 2,2′-bipyridine) acceptor occurs across an organoboron bridge over a distance of approximately 22 Å. Fluoride has a high binding affinity to the organoboron bridge in apolar solutions, and the resulting organofluoroborate has a significantly different electronic structure. We explored to what extent the change from an electron-deficient organoboron wire to an electron-rich organofluoroborate bridge affects long-range electron transfer between the distant triarylamine donor and the Ru(bpy)32+ acceptor. 相似文献
3.
Developing ideal IR probes is essential to understand the structure and dynamics of biomolecules with time-resolved IR spectroscopies and imaging techniques. Especially, nitrile (CN) group has recently been proposed to serve as IR probes of the local environment of proteins. Herein, we investigated the effect of a substituent on the vibrational properties of the benzonitrile. The electron-donating and withdrawing character of p-substituent on benzonitrile are expected to modulate the vibrational frequency, molar extinction coefficient, and vibrational lifetime of CN probe. FT-IR revealed the positive correlation between electron-donating character and the molar extinction coefficient of CN stretch mode. Infrared pump-probe (IR-PP) measurements showed that the vibrational lifetime of CN stretch mode exhibits a relatively weak correlation with the electron-donating strength. Among the investigated samples, 4-dimethylamino benzonitrile with the strongest electron-donating strength shows enhanced absorption and extended vibrational lifetime. Utilizing substituent effects will be a practical strategy to improve the performance of the IR probe. 相似文献
4.
Karel Minnaar 《Journal of the mechanics and physics of solids》2004,52(12):2771-2799
A novel experimental technique is developed for time-resolved detection and tracking of damage in the forms of delamination and matrix cracking in layered materials such as composite laminates. The technique is non-contact in nature and uses dual or quadruple laser interferometers for high temporal resolution. Simultaneous measurements of differential displacement and velocity at individual locations are obtained to analyze the initiation and progression of interfacial fracture and/or matrix cracking/delamination in a polymer matrix composite laminate system reinforced by graphite fibers. The measurements at multiple locations allow the speeds at which interfacial crack front (mode-I) or matrix cracking/delamination front (mode-II dominated) propagates to be determined. Experiments carried out use three-point bend configurations. Impact loading is achieved using a modified Kolsky bar apparatus with a complete set of diagnostics for load, deformation, deformation rate, and input energy measurement. This technique is used to characterize the full process of damage initiation and growth. The experiments also focused on the quantification of the speed at which delamination or damage propagates under primarily mode-I and mode-II conditions. The results show that the speed of delamination (mode-I) or the speed of matrix cracking/delamination (primarily mode-II) increases linearly with impact velocity. Furthermore, speeds of matrix failure/delamination under primarily mode-II conditions are much higher than the speeds of mode-I crack induced delamination under mode-I conditions. 相似文献
5.
激光除漆是一种高效、清洁的新型清洗技术,对激光除漆物理过程和机理的研究是该技术发展的关键。基于LIBS技术,测量得到油漆去除过程中等离子体的发光光谱,计算出油漆样品去除前后等离子体的电子密度和温度,研究了油漆中特征元素对应的光谱特征峰强度随时间的变化情况。结果表明,随着激光作用脉冲数量的增加,油漆去除深度逐渐增加,等离子体电子密度和温度在将漆去除干净的最后几个脉冲作用时呈下降趋势。油漆中Ti元素的所对应的特征峰信号持续时间为2个μs,油漆去除前后信号强度呈现跳跃减少,该现象可用于快速、准确、实时的判断油漆去除情况。 相似文献
6.
Hiroyuki Okamura Hiroki SakaeKeiji Kidani Naoki HirayamaNoboru Aoyagi Takumi SaitoKojiro Shimojo Hirochika NaganawaHisanori Imura 《Polyhedron》2012,31(1):748-753
The extraction constant and the two-phase stability constant (KD,Mβ3) of tris(2-thenoyltrifluoroacetonato)europium(III) between 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C4mim][Tf2N]) as an ionic liquid and an aqueous phase were determined by considering the extraction equilibria including anionic tetrakis(2-thenoyltrifluoroacetonato)europate(III). Specific solute-solvent interactions between the neutral Eu(III) chelate and [C4mim][Tf2N] molecules were revealed from the relationships between the distribution constant of the enol form of 2-thenoyltrifluoroacetone (Htta) as a proton chelate and the distribution constant (KD,M) of the neutral Eu(III) chelate because the [C4mim][Tf2N] system gave the high KD,Mβ3 value compared with those in conventional molecular solvents such as benzene and 1,2-dichloroethane. The coordination environment of Eu3+ in the neutral Eu(III) chelate in [C4mim][Tf2N] was investigated by time-resolved laser-induced fluorescence spectroscopy and infrared absorption spectroscopy. Both methods consistently indicated that not only the Eu(III) chelate extracted but also Eu(tta)3(H2O)3 synthesized as a solid crystal were almost completely dehydrated in [C4mim][Tf2N] saturated with water. Consequently, the higher KD,M or extractability of the neutral Eu(III) chelate in the [C4mim][Tf2N] system can be ascribed to the dehydration of the Eu(III) chelate, which is caused by the specific solvation with [C4mim][Tf2N] molecules. 相似文献
7.
H. Qi D.L. Wang L.M. Ruan 《Journal of Quantitative Spectroscopy & Radiative Transfer》2011,112(15):2507-2519
Particle Swarm Optimization (PSO) algorithms, including standard PSO, Stochastic PSO, and Multi-Phase PSO, are applied to solve the time-domain inverse transient radiation problems in the present research. Time-resolved transmittance and reflectance signals of four different measuring models serve as the measurement data, which estimate absorption, scattering coefficients, and geometric position within one-dimensional non-homogeneous media by inverse simulation. To check retrieval performances and accuracies of PSO-based approaches, four different inverse transient radiation cases are investigated to deal with one homogeneous layer, two-layer, three-layer, and continuous non-homogenous media. The influences of different searching ranges, swarm sizes, and maximum fly velocities on the fitness function of PSO are discussed. Meanwhile, the effects of measurement errors on the reconstruction accuracy are also investigated. All the results confirm that radiative parameters could be estimated accurately with measurement noise using PSO-based approaches. 相似文献
8.
Spectrally dispersed femtosecond time-resolved coherent anti-Stokes Raman spectroscopy is utilized to study the ultrafast vibrational dynamics in rhodamine B dye in solution at room temperature. The anti-Stokes intensities are monitored as a function of time and wavenumber. By simply changing the timing of laser pulses, the vibrational dynamics of excited Raman transitions in rhodamine B molecules can be tracked and detected. 相似文献
9.
10.
Keiko Doi-Kawano Etsuko Nishimoto Yoshiaki Kouzuma Daisuke Takahashi Shoji Yamashita Makoto Kimura 《Journal of fluorescence》2009,19(4):631-639
The steady-state and time-resolved fluorescece spectroscopy is one of the most powerful method to detect and analyze subtle
conformation change and interaction between peptide elements in protein. Phytocystatin Scb isolated from sunflower seeds includes
a single Trp residue at position 85. In an attempt to investigate the interaction of the N-terminal region of Scb with the
first and second hairpin loops by fluorescence spectroscopy of Trp residue, two Scb mutants in which single Trp locates at
position 52 and 58, respectively, and their N-terminal removed mutants were generated. The N-terminal truncation changed the
fluorescence decay kinetics of Trp52 from the triple exponential to double. Furthermore, the time-resolved fluorescence anisotropy
residue indicated that the segmental motion of Trp52 was significantly enhanced by its N-terminal truncation. In contrast,
Trp58 and Trp85 had little influence. The N-terminal successive truncations of Scb and its mutants resulted in the weaken
inhibitors to papain. These results suggested that the N-terminal region of Scb interacts with the peptide segment preceding
the first hairpin loop, thereby stabilizing the conformation of the hairpin loop structure. 相似文献