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101.
Yen‐Chung Chen Jonathan T. B. Huang Kee‐Ching G. Jeng Robin C. K. Yang Mo‐Kai Liao Chee‐Shan Chen Wei‐Jyun Chien Ming‐Tsair Wey Lou‐Sing Kan Leung Sheh 《中国化学会会志》2010,57(2):266-274
To study DNA allostery, quantitative DNase I footprinting studies were carried out on a newly designed peptide His‐Hyp‐Lys‐Lys‐(Py)4‐Lys‐Lys‐NH2 (HypKK‐10) containing the XHypKK (Hyp = hydroxyproline) and polyamide motifs. The interconnection of DNA footprints of peptides HypKK‐10 and the parent peptide PyPro‐12 supports the proposal that interaction network cooperativity is preferred in DNA‐peptide interactions between multiple recognition sites. A simple method of determining interstrand bidentate interactions between the peptide moieties and DNA bases is introduced. It is envisaged that interstrand bidentate interactions also participate in the relay of conformational changes to recognition sites on the complementary strands. Circular dichroism studies of the titration of peptide HypKK‐10 with an oligonucleotide duplex indicate that this peptide binds in a dimeric fashion to DNA in the minor groove. This work may prompt the design of new DNA binding ligands for the study of DNA‐peptide allosteric interactions and DNA interaction network. 相似文献
102.
Liping Lou Yasuhiro Koike Yoshiyuki Okamoto 《Journal of polymer science. Part A, Polymer chemistry》2010,48(22):4938-4942
2,3,4,5,6‐Pentafluoro and 4‐trifluoromethyl 2,3,5,6‐tetrafluoro styrenes were readily copolymerized with methyl methacrylate (MMA) by a free radical initiator. The copolymers were soluble in tetrahydrofuran and acetone. The films obtained were transparent and flexible. The glass transition temperatures (Tgs) of the copolymers were found positively deviated from the Gordon–Taylor equation. The positive deviation could be accounted for by dipole–dipole intrachain interaction between the methyl ester group of MMA and the highly fluorinated aromatic moiety, which resulted in a decrease in the segmental mobility of the polymer chains and the enhanced Tg values of the copolymers. The water absorption of PMMA was greatly decreased by copolymerization of MMA with the highly fluorinated styrenes. With as little as 10 mol % of pentafluoro styrene content in the copolymer, the water absorption was decreased to one‐third of that for pure PMMA. The fluorinated styrenes‐MMA copolymers were thermally stable up to 420 °C under air and nitrogen atmospheres. With 50 mol % of MMA in the copolymer, the copolymer was still stable up to 350 °C. Since these copolymers contain a large number of fluorine atoms, the light absorption in the region of the visible to near infrared is decreased in comparison with nonfluorinated polymers. Thus, these copolymers may be suitable for application in optical devices, such as optical fibers and waveguides. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
103.
Abstract
Nicotinamide crystallizes with 3-hydroxy-2-naphthoic acid and 4-aminobenzoic acid to give rise to cocrystal 1 and 2, respectively. Cocrystal 1, [C11H8O3][C6H6N2O], crystallizes in the monoclinic space group C2/c with a = 25.810(4), b = 4.8932(5), c = 23.869(4) ?, β = 107.078(8)o, V = 2881.6(7) ?3, Z = 8, C17H14N2O4, M r = 310.30, D c = 1.431 g/cm3. Cocrystal 2, [C7H7NO2][C6H6N2O]·H2O, crystallizes in the triclinic space group P-1 with a = 7.214(5), b = 7.326(5), c = 13.484(11) ?, α = 83.23(2), β = 77.189(18), γ = 80.35(2)o, V = 682.7(9) ?3, Z = 2, C13H15N3O4, M r = 277.28, D c = 1.349 g/cm3. Similar carboxylic acid···pyridine synthon R 22(7) can be observed in the two cocrystals. In 1, amide of nicotinamide forms a C(4) chain from the anti H to its carbonyl oxygen. In 2, the amide forms a R 22(8) homodimer which is linked into 2D layer by water molecule through different hydrogen-bonding interactions. The 3D hydrogen-bonded structure results from a synthon R 42(8) from amide, water and amino group of 4-aminobenzoic acid. 相似文献104.
105.
Zhijun Yuan Qihong Lou Jun Zhou Jingxing Dong Yunrong Wei Zhijiang Wang Hongming Zhao Guohua Wu 《Optics & Laser Technology》2009,41(4):380-383
The effect of laser fluence on the crystallization of amorphous silicon irradiated by a frequency-doubled Nd:YAG laser is studied both theoretically and experimentally. An effective numerical model is set up to predict the melting threshold and the optimized laser fluence for the crystallization of 200-nm-thick amorphous silicon. The variation of the temperature distribution with time and the melt depth is analyzed. Besides the model, the Raman spectra of thin films treated with different fluences are measured to confirm the phase transition and to determine the optimized fluence. The calculating results accord well with those obtained from the experimental data in this research. 相似文献
106.
The multi-linear variable separation approach is reviewed in this article. The method has been recently established and successfully
solved a large number of nonlinear systems. One of the most exciting findings is that the basic multi-linear variable separation
solution can be expressed by a universal formula including two (1+1)-dimensional functions, and at least one is arbitrary
for integrable systems. Furthermore, the method has been extended in two different ways so as to enroll more low dimensional
functions in the solution.
相似文献
107.
Qin Lou Matthew A. Kishpaugh Devon A. Shipp 《Journal of polymer science. Part A, Polymer chemistry》2010,48(4):943-951
The synthesis of statistical and block copolymers, consisting of monomers often used as resist materials in photolithography, using reversible addition‐fragmentation chain transfer (RAFT) polymerization is reported. Methacrylate and acrylate monomers with norbornyl and adamantyl moieties were polymerized using both dithioester and trithiocarbonate RAFT agents. Block copolymers containing such monomers were made with poly(methyl acrylate) and polystyrene macro‐RAFT agents. In addition to have the ability to control molecular weight, polydispersity, and allow block copolymer formation, the polymers made via RAFT polymerization required end‐group removal to avoid complications during the photolithography. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 943–951, 2010 相似文献
108.
La (III), Y(III) complexes wit11 diglycol aldehyde his-arginine (H2DAAR) and tetraglycol aldehyde bislysine (H2TALY) Schiff bases were synthesized. Thcy were characterized and formulated as La (H2DAAR) (NO3)3. 6H20 and Y (H2TALY) (NO3)3. 5H20 separately by elemental analyses. The obtained complexes were investigated in detail by high resolution solid state (HRSS)13C NMR using cross polarization, magic angle spinning (CPMAS). and total suppression of sidebands (TOSS) techniques. The results
are supported by the liquid state 2D-’H-13C COSY NMR spectra. Some new information about the splitting peaks of13C for -CH = N- group and alkene carbon bands, etc. in HRSS13C NMR spectra are given. 相似文献
109.
Zi‐Jing Li Hong‐Xiang Lou Wen‐Tao Yu Pei‐Hong Fan Dong‐Mei Ren Bin Ma Mei Ji 《Helvetica chimica acta》2005,88(10):2637-2640
The known 7,8‐secolabdane type diterpenoids neopallavicinin ( 1 ), pallavicinin ( 2 ), and 18‐hydroxypallavicinin ( 3 ) were isolated from Pallavicinia ambigua, and their structures were determined. The X‐ray crystal structure of 1 was solved, and, in combination with CD and NMR studies, the absolute configurations of 1 – 3 were established. A possible biogenetic pathway for 1 and 2 from a single labdane precursor is proposed. 相似文献
110.
Lou van den Dries 《manuscripta mathematica》1999,98(2):133-137
We indicate a complete set of elementary invariants for the ring of Witt vectors over a perfect field of prime characteristic,
where this ring is equipped with its unique multiplicative set of representatives for the residue field.
Received: 31 March 1998 相似文献