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71.
The cationic ruthenium catalyst (Cp*RuCl2)2/AgOTf/Ligand promotes the addition reaction of carboxylic acids across olefins without beta-hydride elimination. 相似文献
72.
Yamamoto Y Arakawa T Ogawa R Itoh K 《Journal of the American Chemical Society》2003,125(40):12143-12160
In the presence of a catalytic amount of Cp*RuCl(cod), 1,6-diynes chemoselectively reacted with monoalkynes at ambient temperature to afford the desired bicyclic benzene derivatives in good yields. A wide variety of diynes and monoynes containing functional groups such as ester, ketone, nitrile, amine, alcohol, sulfide, etc. can be used for the present ruthenium catalysis. The most significant advantage of this protocol is that the cycloaddition of unsymmetrical 1,6-diynes with one internal alkyne moiety regioselectively gave rise to meta-substituted products with excellent regioselectivity. Completely intramolecular alkyne cyclotrimerization was also accomplished using triyne substrates to obtain tricyclic aromatic compounds fused with 5-7-membered rings. A ruthenabicycle complex relevant to these cyclotrimerizations was synthesized from Cp*RuCl(cod) and a 1,6-diyne possessing phenyl terminal groups, and its structure was unambiguously determined by X-ray analysis. The intermediary of such a ruthenacycle intermediate was further confirmed by its reaction with acetylene, giving rise to the expected cycloadduct. The density functional study on the cyclotrimerization mechanism elucidated that the cyclotrimerization proceeds via oxidative cyclization, producing a ruthenacycle intermediate and subsequent alkyne insertion initiated by the formal [2 + 2] cycloaddition of the resultant ruthenacycle with an alkyne. 相似文献
73.
Michio Jimbo Hitoshi Konno Satoru Odake Yaroslav Pugai Jun'ichi Shiraishi 《Journal of statistical physics》2001,102(3-4):883-921
The Wakimoto construction for the quantum affine algebra U $_q$ ( $(\widehat{\mathfrak{s}\mathfrak{l}_2 })$ ) admits a reduction to the q-deformed parafermion algebras. We interpret the latter theory as a free field realization of the Andrews–Baxter–Forrester models in regime II. We give multi-particle form factors of some local operators on the lattice and compute their scaling limit, where the models are described by a massive field theory with $\mathbb{Z}$ $_k$ symmetric minimal scattering matrices. 相似文献
74.
High-brightness 138-W green laser based on an intracavity-frequency-doubled diode-side-pumped Q-switched Nd:YAG laser 总被引:10,自引:0,他引:10
Green power of 138 W was generated at an estimated beam quality of M(2) = 11 by intracavity frequency doubling of a diode-pumped Nd:YAG laser. The laser employs a diffusive close-coupled diode-pumping design and a bifocusing-compensation resonator design to ensure stable operation. 相似文献
75.
T. Watanabe P. Bydžovský K. Dobashi S. Endo Y. Fujii O. Hashimoto T. Ishikawa K. Itoh H. Kanda M. Katoh T. Kinoshita O. Konno K. Maeda A. Matsumura F. Miyahara H. Miyase T. Miyoshi K. Mizunuma Y. Miura S.N. Nakamura H. Nomura Y. Okayasu T. Osaka M. Oyamada A. Sasaki T. Satoh H. Shimizu M. Sotona T. Takahashi T. Tamae H. Tamura T. Terasawa H. Tsubota K. Tsukada M. Ukai M. Wakamatsu H. Yamauchi H. Yamazaki 《Physics letters. [Part B]》2007
76.
T Konno 《Chemical & pharmaceutical bulletin》1990,38(7):2003-2007
Flufenamic acid (FFA) was mixed with magnesium aluminum silicate (MAS) at a reduced pressure of about 10 to 50 mmHg employing a commercial mixer for pharmaceutical production. An amorphous state of FFA in the mixture was efficiently achieved with this equipment, and the dissolution of FFA was enhanced in comparison with that of the physical mixture. Effects of the conditions of mixing, such as pressure, temperature and rotating speed, on dissolution of FFA were determined. Through stability tests at 40 degrees C under both dry and humid conditions, no change in dissolution profiles was recognized in a 5% FFA mixture stored under any conditions. On the other hand, decreases in dissolution behavior were observed in 10% and 20% FFA mixtures when they were stored under humid conditions. These results suggested that humidity should be avoided during the storage of amorphous mixtures of FFA with MAS for production purposes. 相似文献
77.
D.L. Peng T.J. Konno K. Wakoh T. Hihara K. Sumiyama 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2001,16(1):329-332
Cluster-cluster coalescence process of monodispersed Co clusters with mean diameter d = 8.5 and 13 nm deposited a plasma-gas-condensation-type cluster beam deposition system was investigated by in situ electrical conductivity measurements and ex situ scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and analyzed by percolation concept. The electrical
conductivity measurement and TEM observation indicated that, below temperature T≈ 100°C, the Co clusters in the assemblies maintain their original structure as deposited at room temperature, while that the inter-cluster
coalescence takes place at T > 100°C, although the size distribution and the interface morphology of the clusters showed no marked change at substrate temperatures
T
s≤200°C.
Received 29 November 2000 相似文献
78.
Tatsuya Kubokawa Yoshihiko Konno 《Annals of the Institute of Statistical Mathematics》1990,42(2):331-343
For estimating the power of a generalized variance under a multivariate normal distribution with unknown means, the inadmissibility of the best affine equivariant estimator relative to the symmetric loss is shown, and a class of improved estimators is given. The problem of estimating the covariance matrix is also discussed. 相似文献
79.
Prof. Dr. Yoshihiko Yamamoto Kei-ichiro Nishimura Dr. Shota Mori Dr. Masatoshi Shibuya 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(20):5586-5589
In the presence of a cationic Ru catalyst, 1,6-diynes bearing a terminal styryl moiety underwent [2+2+2] cyclization to produce dehydrobiphenylenes fused with a five-membered ring. Although the cycloadducts were unstable toward purification, their one-pot iodine-mediated ring expansion successfully afforded unprecedented bridged ketone products containing a benzo-fused bicyclo[3.2.1] framework. 相似文献
80.
A secretoglobin 3A2 type C (98–139) peptide was synthesized by native chemical ligation between 115Ile and 116Cys residues using Dawson’s linker. The peptide-N-acyl-benzimidazolinone-glycine amide, a C-terminal thioesters precursor, was provided from 3-amino-4-(methylamino)benzoic acid. In addition, an N-terminal cysteine fragment, the (116–139) peptide, was prepared by ordinary Fmoc-solid phase peptide synthesis. Native chemical ligation of the (98–115) fragment with the Dawson’s linker and the (116–139) peptide smoothly proceeded to give SCGB3A2 type C (98–139) peptide. 相似文献