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991.
Qihua Yang Mahendra P. Kapoor Shinji Inagaki Nao Shirokura Junko N. Kondo Kazunari Domen 《Journal of molecular catalysis. A, Chemical》2005,230(1-2):85-89
The first catalytic applications of sulfonic acid-functionalized hydrophobic mesoporous benzene–silica with lamellar pore wall structure are reported. The mesoporous benzene–silica attached with propylsulfonic groups to the crystal-like periodic pore walls exhibited the catalytic activity in the esterification of acetic acid with ethanol. The catalytic results show the higher conversion compared to the commercial Nafion-H. 相似文献
992.
Kotohiro Nomura Yoshitaka Miyamoto Hisao Morimoto Yves Geerts 《Journal of polymer science. Part A, Polymer chemistry》2005,43(23):6166-6177
Factors affecting the syntheses of high‐molecular‐weight poly(2,5‐dialkyl‐1,4‐phenylene vinylene) by the acyclic diene metathesis polymerization of 2,5‐dialkyl‐1,4‐divinylbenzenes [alkyl = n‐octyl ( 2 ) and 2‐ethylhexyl ( 3 )] with a molybdenum or ruthenium catalyst were explored. The polymerizations of 2 by Mo(N‐2,6‐Me2C6H3) (CHMe2 Ph)[OCMe(CF3)2]2 at 25 °C was completed with both a high initial monomer concentration and reduced pressure, affording poly(p‐phenylene vinylene)s with low polydispersity index values (number‐average molecular weight = 3.3–3.65 × 103 by gel permeation chromatography vs polystyrene standards, weight‐average molecular weight/number‐average molecular weight = 1.1–1.2), but the polymerization of 3 was not completed under the same conditions. The synthesis of structurally regular (all‐trans), defect‐free, high‐molecular‐weight 2‐ethylhexyl substituted poly(p‐phenylene vinylene)s [poly 3 ; degree of monomer repeating unit (DPn) = ca. 16–70 by 1H NMR] with unimodal molecular weight distributions (number‐average molecular weight = 8.30–36.3 × 103 by gel permeation chromatography, weight‐average molecular weight/number‐average molecular weight = 1.6–2.1) and with defined polymer chain ends (as a vinyl group, ? CH?CH2) was achieved when Ru(CHPh)(Cl)2(IMesH2)(PCy3) or Ru(CH‐2‐OiPr‐C6H4)(Cl)2(IMesH2) [IMesH2 = 1,3‐bis(2,4,6‐trimethylphenyl)‐2‐imidazolidinylidene] was employed as a catalyst at 50 °C. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 6166–6177, 2005 相似文献
993.
994.
995.
Naoki Kondo Shigeki Kobayashi Hiroyuki Sakaki 《Physica E: Low-dimensional Systems and Nanostructures》2006,32(1-2):49
The self-organized crystal growth of semiconductor quantum rings has opened a new possibility to study and exploit optical transitions between ring-shaped quantum states. In such states, orbital angular momenta of particle envelope functions are well-defined. We investigate theoretically the intraband interlevel transitions between such states and examine the possibility of electrical multipole radiations (EMRs). Selections rules due to envelope function quantum numbers are deduced. To enhance the EMR efficiency, we propose a novel coupled dot–ring structure, by which the lowest allowed EMR can be selected and manipulated, allowing the efficient radiation of multipole photons. 相似文献
996.
In the presence of 5-10 mol% Cp*RuCl(cod), 1,6- and 1,7-diynes were allowed to react with an ethynylboronate at ambient temperature to give rise to bicyclic arylboronates in 64-93% isolated yields. 1,6-Diynes bearing a boronate terminal also underwent cycloaddition with monoalkynes to give the corresponding bicyclic arylboronates. 相似文献
997.
Hisatoshi Kura Hidetaka Oka Masaki Ohwa Tadayoshi Matsumura Akira Kimura Yohei Iwasaki Teruhisa Ohno Michio Matsumura Hisao Murai 《Journal of Polymer Science.Polymer Physics》2005,43(13):1684-1695
Thiol‐substituted α‐aminoalkylphenone was newly developed as a radical photoinitiator. Introduction of the thiol group drastically improved photosensitivity in an alkaline developable resist formulation composed of a prepolymer and a multifunctional acrylate monomer. The improvement in the photocuring speed was explained by a mechanism based on chain transfer reaction of the thiol group. Time‐resolved electron spin resonance (ESR) spectroscopy indicated that the thiol group attached to the chromophore does not influence the photochemical process to generate primary radicals. The photoinitiation of α‐aminoalkylphenone can be spectrally sensitized by 2,4‐diethylthioxanthone (DETX). However, thiol‐substituted α‐aminoalkylphenone showed smaller spectral sensitization than the corresponding compound without a thiol group. Time resolved laser flash photolysis indicated that the rate constant of the quenching of the triplet state of DETX by thiol‐substituted α‐aminoalkylphenone is twice as large as that by the corresponding one without a thiol group. This suggests that, besides energy transfer from DETX in the excited triplet state to the α‐aminoalkylphenone, the thiol group quenches the excited triplet state of DETX via charge transfer and/or hydrogen transfer, as supported by the ESR analysis using a spin trapping technique, and lowers the efficiency of the spectral sensitization effect. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 1684–1695, 2005 相似文献
998.
Keisuke Kobayashi Takeshi Ota Kenzo Maehashi Hisao Nakashima Yoichi Ishiwata Shik Shin 《Physica E: Low-dimensional Systems and Nanostructures》2000,7(3-4)
We introduce a photoluminescence inner core excitation (PLICE) for the studies of semiconductor quantum structures. This novel method, in which we use synchrotron radiation as tunable excitation source, is expected to facilitate us to obtain electronic and compositional information about buried quantum structures. Here we report experimental results on quantum dots (QDs) and quantum wires (QWRs), in order to demonstrate potential applicability of the method to the semiconductor nanostructure studies. 相似文献
999.
Masaya Toda Yoshihiko Kondo Fumio Hamada 《Journal of inclusion phenomena and macrocyclic chemistry》2007,59(3-4):341-344
The supramolecular assembly system based on bis naphtahlene modified β-cyclodextrin dimer linked with ethylenediamine unit
was studied. The synthesis of the titled compound (β-1) was succeeded in a 7% synthetic yield. It was observed that β-1 showed
monomer emission, which was decreased concurrently with appearance of excimer emission in an addition of guest species such
as 1-adamantanol or ursodeoxycholic acid. When γ-CyD was added to the system, two types of fluorescent spectra were obtained,
which was depended on guest species. It was indicated that both of naphthalene units of β-1 were included in the γ-CyD cavity
in the presence of 1-adamantanol in a fashion of 2:1 complex. On the other hand, an addition of ursodeoxycholic acid gave
disappearance of the excimer emission as well as increase of monomer emission. In the system, each of the appended units was
trapped by the each of two γ-CyDs, which is 2:2 complex formation. 相似文献
1000.
A flow-injection procedure combining electrolytic sample decomposition and inductively coupled plasma atomic emission spectrometry (ICP-AES) is proposed in order to rapidly determine the content of silicon in high-silicon electrical steel. This system is characterized by sample decomposition through electrolysis directly coupled to ICP-AES. A steel sample is dissolved by electrolysis using a 6 mol L(-1) HCl solution as an electrolyte with a flow rate of 5 mL min(-1); the electrolyte containing a dissolved sample is subsequently introduced into ICP-AES via a nebulizer. The effects of the electrolysis current and the temperature on the decomposition of the sample were studied. Samples were electrolyzed under the condition of a 1.5 A constant current, at room temperature (25 degrees C) to avoid the hydrolysis of silicon to precipitate. Comparing the analytical results of steel samples obtained by this analytical system with those obtained by the gravimetric method, determined values agreed well quantitatively. The RSD of silicon at approximately 3% was 0.3% (n = 6). 相似文献