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201.
Yoshiyuki?Kimura Hironori?OyaEmail authorView authors OrcID profile 《Algebras and Representation Theory》2018,21(3):589-604
In this paper, we show that quantum twist maps, introduced by Lenagan-Yakimov, induce bijections between dual canonical bases of quantum nilpotent subalgebras. As a corollary, we show the unitriangular property between dual canonical bases and Poincaré-Birkhoff-Witt type bases under the “reverse” lexicographic order. We also show that quantum twist maps induce bijections between certain unipotent quantum minors. 相似文献
202.
We found a new method that a specific interaction between prion, i.e., high-molecular compound, and Cp-60, i.e., low-molecular one, could be successfully elucidated with intermolecular frequency symmetry (IFS). To accomplish this, the former sequence is analyzed with a sequence Fourier analysis used average nuclear (N) resonant frequency scale as a fourth one, and the latter structure with a 13C-NMR software. Further, such the symmetry could be observed in a specific interaction between a segment of human immunodeficiency virus (HIV)gag and PA-457 or between 1918 neuraminidase and peramivir. Therefore, the IFS rule seems to be evolutionarily conserved as a necessary condition even in a specific protein-organic compound interaction. 相似文献
203.
Sang Uck Lee Dr. Jong Chan Kim Hiroshi Mizuseki Prof. Yoshiyuki Kawazoe Prof. 《化学:亚洲杂志》2010,5(6):1341-1346
The structure and the electronic and optical properties of halogenated copper‐phthalocyanine (nα,mβ(Hal)‐CuPc) molecules are investigated, according to the variation in the substituted halogen‐atom species (Hal=Cl or Br) at the α and β positions of isoindole ring with different numbers (n and m=0, 4, 8, or 16). Our results show that the halogen effect mainly results from a structural deformation rather than caused by electronic effects. A nonplanar deformation of the phthalocyanine chromophore of the nα,mβ(Hal)‐CuPc molecule causes a significant change only in the HOMO and HOMO‐1 levels, rather than in the LUMO levels, which leads to the appearance of a green color arising from the large red‐shifts of the Soret and Q bands. The present result may serve as an important reference point for designing novel halogen‐free green pigments, in accordance with the environmental regulations for the restriction of hazardous substances (RoHS) in electronic and electrical devices. 相似文献
204.
Shinnosuke Kamei Yoshiyuki Kojima Nobuyuki Nishimiya 《Journal of luminescence》2010,130(11):2247-2250
This study reports the synthesis of novel red-emitting Eu3+-activated amorphous alkaline earth silicate phosphors with high emission intensities. Eu3+-activated barium (strontium) silicate hydrate phosphors were synthesized using a liquid phase reaction and then heated at 850 °C for 0.5 h to form amorphous barium (strontium) silicate phosphors. These amorphous phosphors emitted in the red region following near-UV (395 nm) irradiation. The internal quantum efficiencies of the Eu3+-activated amorphous barium silicate phosphor and strontium silicate phosphor were 56% and 60%, respectively, even though these phosphors were in the amorphous state. 相似文献
205.
Jun'ichi Katakawa Tadahiro Tetsumi Tadamasa Terai Masaaki Katai Ken-ichi Sakaguchi Masami Kusunoki Mamoru Sato 《Journal of chemical crystallography》2002,32(1-2):39-42
The crystal and molecular structure of a new diterpenyl glycoside, Ptr-1, is presented. The crystal is triclinic, space group P1, with a = 8.2414(8) Å, b = 13.0826(9) Å, c = 6.1427(8) Å, = 95.345(9)°, = 111.589(8)°, = 96.726(7)°, V = 604.9(1) Å3, Z = 1. The structure was solved by direct methods and refined by full-matrix least-squares methods to a final R = 0.049 (Rw = 0.099) for 1872 independent reflections. The molecular structure is based on a glycopyranosyl group and a tetracyclic group. The glycopyranosyl group is -D-allopyranosyl group. The tetracyclic group consists of 1 five-membered and 3 six-membered rings. 相似文献
206.
Katsutoshi Nagai Yoshiyuki Ohishi Hiroshi Inaba Shuichi Kudo 《Journal of polymer science. Part A, Polymer chemistry》1985,23(4):1221-1230
Micellization of cationic salts of dimethylaminoethyl methacrylate (DMAEMA) quaternized with n-alkyl bromides such as octyl, lauryl, myristyl, and stearyl bromide and their polymerizations were investigated. The critical micelle concentration (cmc) in water at 25°C was determined by electrical conductivity and dye(azobenzene) solubilization methods and the relation log(cmc) = 1.46–0.31N was obtained, where cmc is in mmol L?1 and N corresponds to carbon number of alkyl bromides used for the monomer preparations. All of these monomeric salts exhibited a high radical polymerizability in water and benzene. The polymerizations in water appeared to proceed with a higher rate with increasing a chain length of the alkyl moiety of the monomers and those in benzene gave the polymers with a remarkably high viscosity. The rate of polymerization of lauryl bromide salt in anisotropic solutions (in water and benzene) was exceedingly fast as compared with that in isotropic solution(in acetonitrile). All of the polymers obtained here were insoluble in water. Solubility characteristics of these monomers and polymers in other solvents were also presented. The reduced viscosity, in dimethylformamide and methanol, of poly(lauryl bromide salt) prepared in water increased with dilution but that for the polymer obtained in benzene exhibited an inverse concentration dependence. Some discussions were made on the peculiarities of the polymerizations of these monomers and the resulting polymers. 相似文献
207.
Yoshiyuki Hase 《Monatshefte für Chemie / Chemical Monthly》1988,119(4):425-427
TheTeller-Redlich type isotopic product rule within the harmonic approximation is found to be satisfactorily applicable to solid state vibrations of anhydrous lithium nitrate,6LiNO3 and7LiNO3.
Die isotopische Produktenregel für Lithiumnitrat im Festzustand
Zusammenfassung Es wurde festgestellt, daß die Isotopenproduktenregel vomTeller-Redlich-Typ innerhalb der harmonischen Näherung für die Vibrationen von wasserfreiem Lithiumnitrat (6LiNO3 und7LiNO3) im festen Zustand befriedigende Ergebnisse bringt.相似文献
208.
Yonehara F Kido Y Sugimoto H Morita S Yamaguchi M 《The Journal of organic chemistry》2003,68(17):6752-6759
GaCl(3) catalyzes the aromatic alkylation of naphthalene or phenanthrene using cycloalkanes. The C[bond]C formation predominantly takes place at the least hindered positions of the substrates, and equatorial isomers regarding the cycloalkane moiety are generally obtained. The reaction of bicyclo[4.4.0]decane and naphthalene occurs at the 2-position of naphthalene and at the 2- or 3-carbons of the cycloalkane, and the products possess a trans configuration at the junctures and an equatorial configuration at the naphthyl groups. Notably, cis-bicyclo[4.4.0]decane turns out to be much more reactive than the trans isomer, and a turnover number "TON" up to 20 based on GaCl(3) is attained. 1,2-Dimethylcyclohexane reacts similarly, and the cis isomer is more reactive than the trans isomer. Monoalkylcycloalkanes react at the secondary carbons provided that the alkyl group is smaller than tert-butyl. Adamantanes react at the tertiary 1-position. The alkylation reaction is considered to involve the C[bond]H activation of cycloalkanes with GaCl(3) at the tertiary center followed by the migration of carbocations and electrophilic aromatic substitution yielding thermodynamically stable products. The stereochemistry of the reaction reveals that GaCl(3) activates the equatorial tertiary C[bond]H rather than the axial tertiary C[bond]H. 相似文献
209.
Hitoshi Tamiaki Masaaki Amakawa Yoshiyuki Shimono Rikuhei Tanikaga Alfred R. Holzwarth Kurt Schaffner 《Photochemistry and photobiology》1996,63(1):92-99
Abstract— A comparison of the spectra of in vitro (3-hydroxymethyl-131 -oxometallochlorin) and in vivo chlorosomal (bacterio-chlorophyll- c ) aggregates suggests a similar supramolecular structure for the artificial oligomers and the bacte-riochlorophyll- c aggregates in the extramembranous antenna complexes (chlorosomes) of green photosynthetic bacteria. Synthetic zinc and magnesium chlorins have been found to aggregate in 1 % (vol/vol) tetrahydrofuran and hexane solutions and in thin films to form oligomers with the Qy absorption bands shifted to longer wavelengths by about 1900 (Zn chlorins) and 2100 cm−1 (Mg) relative to the corresponding monomer bands. Visible absorption and circular dichroism spectra of various zinc chlorins establish that a central metal, a 31 -hydroxy and a 131 -keto group are functional prerequisites for the aggregation. Vibrational bands measured by IR spectroscopy of solid films reveal two characteristic structural features of the oligomers: (1) a five-coordinated metallochlorin macrocycle with an axial ligand (bands at 1500-1630 cm−1 ), and (2) a hydrogen bond between the keto oxygen of one chlorin and the hydroxy group of a second chlorin, the oxygen of which is chelated to the metal atom of a third molecule, i.e . C=O…H-O…M (=Zn or Mg). 相似文献
210.
Hydrolysis and Condensation Processes of Titanium iso-Propoxide Modified with Catechol: An NMR Study
Egawa Kentaro Suzaki Kentaro Sugahara Yoshiyuki 《Journal of Sol-Gel Science and Technology》2004,30(2):83-88
The hydrolysis and condensation processes of titanium iso-propoxide modified with catechol (C6H4(OH)2; H2cat) have been investigated by 1H, 13C and 17O nuclear magnetic resonance spectroscopy. The hydrolysis reactions of the modified titanium iso-propoxide in the system with Ti:tetrahydrofuran (THF):H2O = 1:20:x (x = 1, 2 and 5 in a molar ratio) are essentially completed in the initial stage (<1 h), and the condensation reactions also proceed significantly during this stage. Upon hydrolysis with H2O/Ti = 1, the iso-propoxy groups are selectively hydrolyzed and the catecholate groups remain bound to titanium. With H2O/Ti = 2 and 5, both the iso-propoxy and catecholate groups are hydrolyzed, and the hydrolysis of the iso-propoxy groups is relatively preferential. Approximately half the catecholate groups are stably bound to titanium, even after hydrolysis with H2O/Ti = 5. 相似文献