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991.
A novel copolymer, poly(N‐hexyl‐3,7‐phenothiazylene‐1,2‐ethenylene‐2,6‐pyridylene‐1,2‐ethenylene) ( P3 ), containing N‐hexyl‐3,7‐phenothiazylene and 2,6‐pyridylene chromophores was synthesized to investigate the effect of protonation, metal complexation, and chemical oxidation on its absorption and photoluminescence (PL). Poly(N‐hexyl‐3,8‐iminodibenzyl‐1,2‐ethenylene‐1,3‐phenylene‐1,2‐ethenylene) and poly(N‐hexyl‐3,7‐phenothiazylene‐1,2‐ethenylene‐1,3‐phenylene‐1,2‐ethenylene) ( P2 ), consisting of 1,3‐divinylbenzene alternated with N‐hexyl‐3,8‐iminodibenzyl and N‐hexyl‐3,7‐phenothiazylene, respectively, were also prepared for comparison. Electrochemical investigations revealed that P3 exhibited lower band gaps (2.34 eV) due to alternating donor and acceptor conjugated units (push–pull structure). The absorption and PL spectral variations of P3 were easily manipulated by protonation, metal chelation, and chemical oxidation. P3 displayed significant bathochromic shifts when protonated with trifluoroacetic acid in chloroform. The complexation of P3 with Fe3+ led to a significant absorption change and fluorescence quenching, and this implied the coordination of ferric ions with the 2,6‐pyridylene groups in the backbone. Moreover, both phenothiazylene‐containing P2 and P3 showed conspicuous PL quenching with a slight redshift when oxidized with NOBF4. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1272–1284, 2004 相似文献
992.
Two new compounds have been isolated from the whole plant of Monochoria vaginalis and characterized as: (10Z)‐1‐(2,6‐dihydroxyphenyl)octadec‐10‐en‐1‐one ( 1 ) (20R, 24R)‐campest‐5‐ene‐3β, 4β‐diol ( 2 ) together with nine known ones. The structures of these compounds were elucidated on the basis of spectral data and chemical evidence. 相似文献
993.
Emrys A. Jones Nicholas P. Lockyer John C. Vickerman 《International journal of mass spectrometry》2007,260(2-3):146
Recent developments in desorption/ionisation mass spectrometry techniques have made their application to biological analysis a realistic and successful proposition. Developments in primary ion source technology, mainly through the advent of polyatomic ion beams, have meant that the technique of secondary ion mass spectrometry (SIMS) can now access the depths of information required to allow biological imaging to be a viable option.Here the role of the primary ion C60+ is assessed with regard to molecular imaging of lipids and pharmaceuticals within tissue sections. High secondary ion yields and low surface damage accumulation are demonstrated on both model and real biological samples, indicating the high secondary ion efficiency afforded to the analyst by this primary ion when compared to other cluster ion beams used in imaging. The newly developed 40 keV C60+ ion source allows the beam to be focused such that high resolution imaging is demonstrated on a tissue sample, and the greater yields allow the molecular signal from the drug raclopride to be imaged within tissue section following in vivo dosing.The localisation shown for this drug alludes to issues regarding the chemical environment affecting the ionisation probability of the molecule; the importance of this effect is demonstrated with model systems and the possibility of using laser post-ionisation as a method for reducing this consequence of bio-sample complexity is demonstrated and discussed. 相似文献
994.
995.
A. I. Golovashkin G. N. Izmaïlov G. V. Kuleshova T. Q. Khánh A. M. Tskhovrebov L. N. Zherikhina 《The European Physical Journal B - Condensed Matter and Complex Systems》2007,58(3):243-249
A scheme of magnetic calorimeter for registration of rare events
characterized by small energy release (cosmic rays, WIMPs, solitary X-ray
quanta) is proposed. The calorimeter is brought to operation by adiabatic
demagnetization, and its magnetic response is measured by a quantum
interferometer (SQUID, A. Barone and G. Paterno, Physics and applications of Josephson Effect). Special consideration is given to the specific
features of calorimeter operation in the ferromagnetic transition region.
The trigger registration of ultrasmall energy release by a ferromagnetic
system in the metastable state is described. 相似文献
996.
997.
We characterize the sequences of orthogonal polynomials on the unit circle whose derivatives are also orthogonal polynomials on the unit circle. Some relations for the sequences of derivatives of orthogonal polynomials are provided. Finally, we pose some problems about orthogonality-preserving maps and differential equations for orthogonal polynomials on the unit circle. 相似文献
998.
M. H. Gehlen M. Van der Auweraer F. C. De Schrwer 《Photochemistry and photobiology》1991,54(4):613-618
The luminescence decay of excited probes in micelles in the presence of a Poisson distribution of quenchers is considered under conditions where both probe and quencher within the lifetime of the excited probe may exchange between the micelles. Analytical and numerical results show that the luminescence decay can be expressed by a generalized self convolution product of a multiexponential decay function. 相似文献
999.
1000.
D. Guyomard C. Pagnoux J. J. Zah Letho A. Verbaere Y. Piffard 《Journal of solid state chemistry》1991,90(2)
The single phase compound Na3SbO(PO4)2 was prepared by a solid state reaction. It crystallizes in the orthorhombic system, space group P212121 with a = 6.964(1) Å, b = 9.284(2) Å, c = 12.425(2) Å, Z = 4. The structure was determined from 968 reflections collected on a Nonius CAD4 automatic diffractometer with MoKα radiation. The final R index and weighted Rw index are 0.031 and 0.039, respectively. The structure is built up from strings of corner-sharing SbO6 octahedra to which phosphate groups are linked by two of their vertices. These chains, running parallel to the a-axis, are separated from each other by sodium atoms. 相似文献