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221.
Tadeusz Jankowski 《Journal of Mathematical Analysis and Applications》2007,332(2):1380-1392
In this paper we deal with second order differential equations with causal operators. To obtain sufficient conditions for existence of solutions we use a monotone iterative method. We investigate both differential equations and differential inequalities. An example illustrates the results obtained. 相似文献
222.
Smith RF Eggert JH Jankowski A Celliers PM Edwards MJ Gupta YM Asay JR Collins GW 《Physical review letters》2007,98(6):065701
A laser-produced x-ray drive was used to shocklessly compress solid aluminum to a peak longitudinal stress of 110 GPa within 10 ns. Interface velocities versus time for multiple sample thicknesses were measured and converted to stress density (Px-rho) using an iterative Lagrangian analysis. These are the fastest shockless compression Px(rho) results reported to date, and are stiffer than models that have been benchmarked against both static and shock-wave experiments. The present results suggest that at these short time scales there is a higher stress-dependent strength and a stiffer time-dependent inelastic response than had been expected. 相似文献
223.
In this paper, we present gold-plating polycarbonate (PC) microchannels. The fabrication of the gold microfluidic channels is achieved by tuning the sequence of reagent insertion into milled and closed submillimeter PC system channels. The resulting gold surface can be utilized in many applications where the benefits of microfluidics, (bio)chemistry of surfaces, and electrochemistry can be combined. Here, we combine the advantages of electrochemistry with microfluidics by mixing the gold sensor with microfluidics. This approach differs from the classic one – the sensor will undergo modifications (e. g., shape and size) depending on the specific scientific problem and will be designed individually; hence its characteristics will be changed. Our goal in this work is to indicate new possibilities for combining two methodologies – electrochemistry and microfluidics. In our work, we emphasize that it confirms the validity of our chosen concept (proof-of-concept). In this work, we present one such application, the use of a gold microfluidic channel as a working electrode (WE). We describe the microchip‘s construction and electrochemical characterization, including the gold flow-through WE, the Ag/AgCl wire pseudo-reference, and the Pt auxiliary electrode. The measured current is the result of the flow through a rectangular duct of the gold microchannel electrode embedded in the four walls of the chip. 相似文献
224.
Cyphersmith A Surampudi S Casey MJ Jankowski K Venkataraman D Barnes MD 《The journal of physical chemistry. A》2012,116(22):5349-5352
We report on the single-molecule chiroptical properties of "right"-handed bridged triaryl amine helicene dimers, MH2. Using an experimental setup to precisely define the circular excitation polarization at the sample plane, we investigated the circular dichroic response in luminescence from individual molecules in which induced ellipticity from microscope optics is minimized. Our results comparing circular anisotropies in fluorescence excitation from MH2 and perylene diimide (PDI), an achiral, centrosymmetric chromophore, demonstrate a significant reduction in the breadth of the distribution of circular dissymmetry parameters obtained from modulation of the circularly polarized excitation source (457 nm). For PDI, we observe a symmetric distribution of circular anisotropy parameters centered about zero, with a fwhm of 0.25. For MH2, we observe an asymmetric distribution peaked at g = -0.09, with a slightly larger width as the corresponding PDI distribution. These results indicate that the large dissymmetry parameters (|g| > 0.5) in fluorescence excitation described in our original report (Hassey, R.; et al. Chirality 2008, 20, 1039-1046 and Hassey, R.; et al. Science 2006, 314, 1437-1439) were indeed affected by (at the time, unknown) linear polarization artifacts. However, the present results on MH2 provide compelling evidence for single-molecule circular dissymmetries much larger than solution or thin-film ensemble values, defined primarily by the enhanced rotatory strength (relative to the monomer), and restricted orientation at the sample surface. 相似文献
225.
Jan Jankowski 《Rendiconti del Circolo Matematico di Palermo》2006,55(1):95-102
We show the existence of absolutely continuous extremal solutions to the problemx′(t)=f(t, x)h(t)))+g(t)),x(0)=x
0, whereh is an arbitrary continuous deviated argument. Conditions for the uniqueness of solutions are given.
Research partialy supported by grant UG BW 5100 - 5 - 0143 - 4 相似文献
226.
Flavia Jankowski 《Tetrahedron》2010,66(1):128-133
A general method has been developed for the synthesis of 1,3-disubstituted-imidazo[1,5-a]quinazolin-5-(4H)-ones. This process involves initial microwave-assisted quinazolinone formation between anthranilamide and various Boc- or acylamino acids, followed by intramolecular cyclodehydration under acidic conditions. In the case of 3-monosubstituted-imidazoquinazolinones, the procedure needs the formation of the formamide derivatives by deprotection and formylation of the Boc-intermediates. 相似文献
227.
J Katarzyńska A Mazur WM Wolf SJ Teat S Jankowski MT Leplawy J Zabrocki 《Organic & biomolecular chemistry》2012,10(33):6705-6716
This paper presents the synthesis and solution conformational studies of the tripeptides Fmoc-Ala-(R)-(αMe)Ser(Ψ(H,H)Pro)-Ala-OBu(t) (6a) and Fmoc-Ala-(S)-(αMe)Ser(Ψ(H,H)Pro)-Ala-OBu(t) (6b). Additionally, the X-ray structure of 6a is given. NMR analysis corroborated by theoretical calculations (XPLOR) shows that in both peptides the amide bond between pseudoproline and the preceding amino acid is in the trans conformation. The same amide bond geometry was observed in the crystal state of 6a. The latter is additionally influenced by the presence of two symmetrically independent molecules in an asymmetric unit. Both molecules adopt a conformation which resembles β-turn type II, stabilized by hydrogen bonding. The conformational preferences and prolyl cis-trans isomerization of Ac-(αMe)Ser(Ψ(H,H)Pro)-NHMe (7) were explored at the IEFPCM/B3LYP/6-31+G(d) level of theory in vacuum, water and chloroform. It has been shown that the trans isomer predominates in water solutions and the cis isomer is preferred in chloroform. The conformation of 7 is down-puckered independently of the geometry of the amide bonds, with lower puckering in the transition state of the cis-trans isomerization. 相似文献
228.
Piotr Jankowski Claire L. McMullin Ilya D. Gridnev A. Guy Orpen Paul G. Pringle 《Tetrahedron: Asymmetry》2010,21(9-10):1206-1209
The enantioselective hydrogenation catalyst [Rh(α-CgPH)2(cod)]BF4, (CgPH = 6-phospha-2,4,8-trioxa-adamantane) exists in solution as a mixture of two slowly interconverting rotamers, one with C2- and the other with C1-symmetry. 相似文献
229.
Louis D. Quin Ryszard Bodalski Stefan Jankowski GyOungyi S. Quin Narayan D. Sadanani Xiao-Ping Wu 《Heteroatom Chemistry》1991,2(1):99-110
The 2,3-oxaphosphabicyclo[2.2.2]octene 3-oxide (or sulfide) ring system is of considerable value because it easily fragments on being heated or irradiated (254 nm) to provide three-coordinate phosphoryl species. The system is synthesized by O-insertion with peracids into a C P bond of 7-phosphanorbornene derivatives with a variety of P-substituents. With rare exception, the insertion has been found to proceed with retention of the configuration at phosphorus, as established by X-ray and NMR techniques. The thermal fragmentation that produces the metaphosphate derivatives EtO PO2, EtO P(S)O, and Et2N PO2 follows first-order kinetics, and is independent of the concentration of a trapping agent for these species. Solvent effects and activation parameters join in defining a retrocycloaddition mechanism that ejects the free metaphosphate. The species Ph PO2 can also be easily generated either thermally or photochemically. Metaphosphates have been found to attack ethereal oxygen in epoxides and oxetanes, and may undergo anchimeric participation with a properly placed methoxy group on the substituent used in the 2,3-oxaphosphabicyclo[2.2.2]octene precursor. 相似文献
230.
In the paper the influence of geometry of the body region for the rate of initial temperature evolution is shown. Free exchange of the boundary temperature was assumed. There was also investigated the influence of the Biot coefficient on the heat conduction process course. Generalisation of the fictitious sources method for the inhomogeneous initial condition was made. 相似文献