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71.
72.
Anion complexation. A ditriphenylphosphonium calix[4]arene derivative as a novel receptor for anions
A novel anionic receptor 2 consisting of a calix[4]arene bearing two alkytriphenylphosphonium has been prepared by two different procedures. The complexation occurred at the phosphonium sites probably due to electrostatic and/or π-anion forces. 相似文献
73.
Ryu Sasaki 《Czechoslovak Journal of Physics》2003,53(11):1111-1117
The relationship (resemblance and/or contrast) between quantum and classical integrability in Ruijsenaars-Schneider (R-S) and Calogero-Moser systems is addressed. The classical Calogero and Sutherland systems (based on any root system) at equilibrium have many remarkable properties; for example, the minimum energies, frequencies of small oscillations and the eigenvalues of Lax pair matrices at equilibrium are all integer valued. These are related to the energy eigenvalues of the quantum Calogero and Sutherland systems. Similar features and results hold for the R-S type of integrable systems based on the classical root systems. 相似文献
74.
Photoelectrochemical decomposition of water on nanocrystalline BiVO4 film electrodes under visible light 总被引:1,自引:0,他引:1
Sayama K Nomura A Zou Z Abe R Abe Y Arakawa H 《Chemical communications (Cambridge, England)》2003,(23):2908-2909
The nanocrystalline BiVO4 film electrode on conducting glass showed an excellent efficiency (IPCE = 29% at 420 nm) for the decomposition of water under visible light. 相似文献
75.
Studer A Amrein S Matsubara H Schiesser CH Doi T Kawamura T Fukuyama T Ryu I 《Chemical communications (Cambridge, England)》2003,(10):1190-1191
4-[(Trimethylstannyl)diphenylsilyl]butanoyl radical, arising from the corresponding 3-(stannylsilyl)propyl radical and CO, undergoes an SHi reaction at Si with extrusion of trimethyltin radical to give silacyclopentanone. The parent 3-(stannylsilyl)propyl radical was also found to isomerize to (3-stannylpropyl)silyl radical via a 1,4-Sn shift from Si to C with a rate constant of 9.3 x 10(4) s-1 at 80 degrees C. Ab initio and DFT MO calculations support a front-side attack mechanism. 相似文献
76.
Koike R Motoyoshiya J Takaguchi Y Aoyama H 《Chemical communications (Cambridge, England)》2003,(6):794-795
A kinetic study of peroxyoxalate chemiluminescence reactions employing 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates supports the 1,2-dioxetanones still bearing the eliminating group as the key intermediates that interact with the fluorophores rather than 1,2-dioxetanedione. 相似文献
77.
Yamasaki R Tanatani A Azumaya I Saito S Yamaguchi K Kagechika H 《Organic letters》2003,5(8):1265-1267
[reaction: see text] Introduction of an electron-withdrawing group on the aromatic ring of N-methylacetanilide decreased the ratio of the cis conformer, and the ratio correlates well with the Hammett sigma values of the substituents. These steric properties can be applied to achieve amide conformational switching by protonation at the aromatic substituent of 4-[bis(dimethylamino)]-N-methylacetanilide or N-[p-(dimethylamino)phenyl]-N-phenylacetamide. 相似文献
78.
Yanghyun?ByunEmail author Dosang?Joe Jeong?Seog Ryu Seunghun?Yi 《Mathematische Zeitschrift》2003,245(3):435-453
We investigate the possibility of a Lagrangian Whitney trick, a process to remove a pair of intersection points of a self-transverse Lagrangian immersion by a homotopy through Lagrangian immersions. There is a model for which a Lagrangian Whitney trick with compact support works assuming the model satisfies an area-capacity condition. Reduction of more general cases to the model, not necessarily fulfilling the area-capacity requirement, is possible if the given pair of double points admits a suitable symplectic disc and a certain Maslov-Viterbo index is 1. We look into an example to see the actualities of the Maslov-Viterbo index and the area-capacity conditions.
The authors would like to thank the anonymous referee whose suggestions improved remarkably the exposition of the paper. This work was supported by the grant no.R01-2000-000-00004-0 from Korea Science & Engineering Foundation. 相似文献
79.
Young-Kwon Park Hyung Won Lee Jong-Ki Jeon Seung-Soo Kim Changkook Ryu Ji Man Kim Ho-Jeong Chae Kwang-Eun Jeong 《Research on Chemical Intermediates》2011,37(9):1283-1291
The catalytic cracking of oil fractions separated from summer food waste leachate was investigated over BEA zeolite and Al-SBA-15 catalysts. In this study, a mixture of food waste oil fractions and catalyst was directly introduced to pyrolysis gas chromatography/mass spectrometry (Py-GC/MS), with the resulting vapor phase products being simultaneously analyzed. Various acid compounds, including oleic acid, produced by the non-catalytic pyrolysis of food waste leachate were reformed into valuable compounds, such as oxygenates, hydrocarbons, and aromatics. The BEA zeolite catalyst showed higher selectivity for hydrocarbon compounds, especially aromatics, within the gasoline range due to its superior cracking ability originating from its highly acidic sites. Conversely, the cracking performance of the Al-SBA-15 catalyst, possessing mild acidic sites, was lower than that of the BEA zeolite. Increasing the amount of Al-SBA-15 catalyst enhanced the cracking activity and resulted in higher selectivity for hydrocarbons. 相似文献