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171.
To explore the anion recognition ability of silanol derivatives, ESI-MS and 1H NMR titrations of a 1,3-disiloxanediol 1 with anions were studied in CDCl3 and MeCN-d3. The results indicate that 1 showed strong binding to anions such as AcO− and halides. 相似文献
172.
Hasegawa Y Fukuda T Hagimori K Tomoda H Omura S 《Chemical & pharmaceutical bulletin》2007,55(9):1338-1341
Six new alkylitaconic acids, designated tensyuic acids A to F, were isolated from the culture broth of Aspergillus niger FKI-2342 by solvent extraction, silica gel column chromatography and HPLC. Their structures were elucidated by spectroscopic analysis including UV, NMR, and MS. They are all alkylitaconic acid derivatives. Only tesyuic acid C showed moderate antimicrobial activity against Bacillus subtilis. 相似文献
173.
Nagamitsu T Takano D Marumoto K Fukuda T Furuya K Otoguro K Takeda K Kuwajima I Harigaya Y Omura S 《The Journal of organic chemistry》2007,72(8):2744-2756
The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two segments. A detailed examination of the macrocyclization led us to the samarium(II) iodide-mediated intramolecular Reformatsky-type reaction as the most efficient synthetic approach. The two key segments were synthesized through regioselective methylation, directed hydrogenation, stereoselective Reformatsky-type reaction, and MgBr2.Et2O-mediated chelation-controlled allylation. 相似文献
174.
Matsuta K. Onishi T. Fukuda M. Minamisono T. Mihara M. Sasaki M. Yamaguchi T. Miyake T. Sato K. Minamisono K. Ohsumi F. Muramoto Y. Oui S. Ha C. Tanaka K. Kidera K. Morishita A. Tsubota T. Sumikama T. Kitagawa A. Torikoshi M. Kanazawa M. Nishio T. Koda S. Ohtsubo T. Fukuda S. Nojiri Y. Momota S. Ozawa A. Yoshida K. Suzuki T. Kobayashi T. Tanihata I. Hanna S.S. Alonso J.R. Krebs G.F. Symons T.J.M. 《Hyperfine Interactions》1999,120(1-8):713-717
The degrees of nuclear spin polarization of 8,12B, 9C, 12N, 13O, 20,21F, 23Mg, 27Si and 39Ca produced in the high energy 12,13C, 16O, 22Ne, 24Mg, 28Si and 40Ca ions on Be collisions have been measured systematically, for the technical developments of the nuclear moment studies as
well as the hyperfine interaction studies by means of β-NMR technique. The fragment momentum dependences were well reproduced
by the simple kinematical model. Incident energy dependence and the mass dependence as well as the reaction angle dependences
were qualitatively explained by the mixing of the near and far side collisions.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
175.
Shuhei Fukawa Masahiko Hada Ryoichi Fukuda Shinji Tanaka Hiroshi Nakatsuji 《Journal of computational chemistry》2001,22(5):528-536
Linear and nonlinear halogen dependencies of the 13C magnetic shielding constants of CH4−nIn, CH4−nBrn, CCl4−nIn, and CBr4−nIn were fairly reproduced by the ab initio generalized unrestricted Hartree–Fock (GUHF)/finite perturbation (FP) method including spin‐orbit (SO) interaction and spin‐free relativistic (SFR) terms. As seen from the experimental trends, the calculated 13C chemical shifts in CCl4−nIn and CBr4−nIn depend linearly on n=0–4, while those in CH4−nIn and CH4−nBrn depend nonlinearly. We found that both the linear and nonlinear dependencies are due to the relativistic effects, and especially due to the Fermi–Contact (FC) term originating from the SO interaction. © 2001 John Wiley & Sons, Inc. J Comput Chem 22: 528–536, 2001 相似文献
176.
Kenji Yamada Masahiko Minoda Takeshi Fukuda Takeaki Miyamoto 《Journal of polymer science. Part A, Polymer chemistry》2001,39(4):459-467
Amphiphilic block and statistical copolymers of vinyl ethers (VEs) with pendant glucose residues were synthesized by the living cationic polymerization of isobutyl VE (IBVE) and a VE carrying 1,2:5,6‐di‐O‐isopropylidene‐D ‐glucose (IpGlcVE), followed by deprotection. The block copolymer was prepared by a two‐stage sequential block copolymerization, whereas the statistical copolymer was obtained by the copolymerization of a mixture of the two monomers. The monomer reactivity ratios estimated with the statistical copolymerization were r1 (IBVE) = 1.65 and r2 (IpGlcVE) = 1.15. The obtained statistical copolymers were nearly uniform with the comonomer composition along the main chain. Both the block and statistical copolymers had narrow molecular weight distributions (weight‐average molecular weight/number‐average molecular weight ∼ 1.1). Gel permeation chromatography, static light scattering, and spin–lattice relaxation time measurements in a selective solvent revealed that the block copolymer formed multimolecular micelles, possibly with a hydrophobic poly(IBVE) core and a glucose‐carrying poly(VE) shell, whereas the statistical copolymer with nearly the same molecular weight and segment composition was molecularly dispersed in solution. The surface properties of the solvent‐cast films of the block and statistical copolymer were also investigated with the contact‐angle measurement. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 459–467, 2001 相似文献
177.
The structural phase transition between the polymorphs of syndiotactic polystyrene has been studied by means of molecular dynamics simulation. It was found that the initial δe form of the crystal structure was completely transformed into the γ form by thermal treatment. Not only the crystal structure but also the transition path are investigated at the molecular level for the first time. 相似文献
178.
Yuzo Ishigaki Koji Takahashi Hiroyuki Fukuda 《Macromolecular rapid communications》2000,21(15):1024-1027
The polymerization of zinc methacrylates coordinated with a bidentate ligand ( 1 – 4 ) was carried out in chloroform at 60°C. The polymerization of these monomers gave chloroform‐insoluble polymers. Stereoregularity of the polymers was estimated from 1H NMR spectra of poly(methyl methacrylate)s (PMMAs) derived from the original polymers. Monomers 1 and 2 gave slightly different polymers compared with conventional ones obtained by polymerization of methacrylic acid, while 3 afforded higher amounts of isotactic polymers than 1 and 2 . Conversely, 4 gave a polymer of high syndiotacticity. Furthermore, the relationship between triad tacticity and monomer concentration in the feed was studied. Consequently, it was demonstrated that the structure of bidentate ligands coordinated with zinc ion influences the stereoregularity of the resulting polymers. 相似文献
179.
V. V. Kochurikhin K. Shimamura B. M. Epelbaum H. Takeda T. Fukuda 《Crystal Research and Technology》1998,33(1):65-70
The automatic diameter control system using the results of spectral analysis of weight sensor data as a criterion for the amount of feedback tuning was applied successfully for the growth of La3Ga5SiO14 single crystals. The developed method enabled to determine timely the appearance of oscillations in the control system and to adapt the amplification factor automatically for the maintenance of stable crystal shape. Furthermore, the developed system made it possible to estimate the formation of a second phase at a very early stage. 相似文献
180.
The reaction of 3-methyl-2-methylene-1,3-oxazolidine ( 1a ) and phenylisothiocyanate (PhNCS) gives 3-methyl-2-(phenylthiocarbamoyl)methylene-1,3-oxazolidine ( 3 ) whereas that of 2-isopropylidene-3-methyl-1,3-oxazolidine ( 1b ) and PhNCS gives 1:1 alternating copolymers. It is assumed that the reaction of 1b and PhNCS forms a zwitterionic intermediate ( 2b ), followed by the successive combination of 2b to give 1:1 alternating copolymers 4 and/or 5 . Consequently, it was demonstrated that the copolymerization of 1b and PhNCS proceeds via a zwitterionic mechanism with complete ring-opening to afford the 1:1 alternating copolymer 5 . 相似文献