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211.
Pradip K. Bhowmik Haesook Han Ivan K. Ndedeltchev James J. Cebe Shin‐Woong Kang Satyendra Kumar 《Liquid crystals》2013,40(8):891-906
Several viologen bis{tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate} salts were prepared by metathesis reaction of the corresponding viologen dibromides (diiodide) with sodium bis{tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate} salt in a polar organic solvent. They were characterized for their physical and thermal properties by experimental techniques including variable temperature X‐ray diffraction. All exhibited low T g and T m, and their T g/T m (K) ratios were in the range 0.66–0.79. Several exhibited polymorphism and formed isotropic ionic melts at <150°C. They were soluble in many common organic solvents such as ethers, alcohols, acetonitrile and methylene chloride. They exhibited photoluminescence in both 1,2‐dimethoxyethane and methanol, as well as in the solid state. In the solid state, the emission spectra exhibited hypsochromic shift when compared with those in solutions of 1,2‐dimethoxyethane and methanol. 相似文献
212.
Leonel M. Chiacchiarelli Ivan Puri Debora Puglia José M. Kenny Luigi Torre 《Colloid and polymer science》2013,291(12):2745-2753
The tensile properties and structure of silica-based polyurethane (PU) nanocomposites were parametrically studied as a function of silica type and weight concentration, polyol OH number, and mixing methods. The variation of the silica functionalization groups (from silanols to silazanes) had a relevant effect on dispersion. An elevated interparticle distance of the silica agglomerates improved substantially the tensile strength (from 44.3 to 82.8 MPa) and strain to failure (from 3.0 to 7.95) while maintaining elastic modulus (from 2.08 to 2.31 GPa) with respect to the neat PU matrix. Polyol’s with different OH numbers have shown to dramatically modify the silica dispersion degree by the modification of the stability of the colloidal dispersion. An increase of its value deteriorated dispersion and the tensile properties of the nanocomposites. The effect of three dispersion methods (ultrasonic dispersion, high shear mixing, and tip sonication) has shown to have a relative effect on the reduction of agglomerate size and the interparticle distance. High power sonication methods were more effective in reducing agglomerate size in contrast to shear methods. Classical theories of colloidal dispersion (Derjaguin, Landau, Verwey, and Overbeek) have been able to explain the correlation between the silica aggregation state and the final tensile properties of the nanocomposite. 相似文献
213.
Methyl methacrylate and styrene copolymers containing pendant benzil groups, such as 1-[4-(2-methacroyloxyethoxy)phenyl]-2-phenyl-1,2-ethanedione-co-methyl metacrylate (BzMA/MMA), 1-[4-(2-methacroyloxyethoxy)phenyl]-2-phenyl-1,2-ethanedione-co-styrene (BzMA/S), and 1-phenyl-2-(4-propenoylphenyl)-1,2-ethanedione-co-styrene (PCOCO/S), were prepared and used as precursors for photochemically generated pendant benzoyl peroxides. Decomposition of the pendant benzoyl peroxides was subsequently used in grafting processes. Either irradiation or a combination of irradiation with subsequent thermal treatment was adopted for grafting a thin layer of BzMA/MMA copolymer onto the surface of LDPE films. The grafting resulted in a significant decrease in contact angle of the film surface. The same activation strategy was successfully adopted to initiate the polymerisation of acrylic or methacrylic acids from the surface of styrene copolymer films containing the initiator precursor in the polymer side chains (BzMA/S and PCOCO/S). The successful surface grafting was proved by contact angles measurement as well as by infrared spectroscopic analysis. 相似文献
214.
The synthesis of the aliphatic subunit 9 of the macrolide LL‐Z1640‐2 (I), starting from a 4‐deoxy‐D‐mannose derivative 2a, is described. The procedure includes the first successful application of a Vasella ring opening reaction for a 4‐deoxypyranoside. Nucleophilic addition of an alkynyllithium reagent to the aldehyde 4 led to the propargylic alcohol 7, which was converted to the advanced building block 9 in two further steps. 相似文献
215.
216.
Ivan N. Bardasov Anastasiya U. Alekseeva Denis L. Mihailov Oleg V. Ershov Oleg E. Nasakin Viktor A. Tafeenko 《Tetrahedron letters》2014
The synthesis of 2-(dicyanomethylene)-1,2-dihydropyridine derivatives from the reactions of arylmethylidene derivatives of malononitrile dimers with 1,3-dicarbonyl compounds is described. 相似文献
217.
Senka Djaković Ivan Kodrin Vilko Smrečki Predrag Novak Zlatko Mihalić Dinko Žiher Jasmina Lapić Vladimir Rapić 《Tetrahedron》2014
In this study we present a synthesis and conformational analysis of 1′-acetylferrocene amino acid derivatives of type Ac–Fn–CO–AA–Y (Fn=ferrocene-1,1-diyl; AA=Gly, Ala or Val; Y=OMe or NHMe) as a simple model for parallel β-helical peptides. Derivatives with only one amino acid adopt a reduced number of total conformations and allow a more exact analysis of intramolecular hydrogen bonds (IHB) close to the ferrocene unit. Conformational analysis of these bioconjugates was performed by a combination of spectroscopic techniques (IR, NMR and CD) and corroborated by solution-phase DFT calculations. The investigation of ester conjugates 1–3 indicates the coexistence of non-bonded (an open forms) and hydrogen bonded NHa group forming a 7-membered ring (γ-turn). The amide derivatives 4–6 with an additional NHb hydrogen bond donor are mostly constituted of conformers with a 10-membered ring (β-turn) as a single IHB pattern or the β-turn accompanied by a 7-membered ring (γ-turn) containing NHa group. The exchange of the amino acid side-chain does not significantly affect the conformational properties and IHB pattern of the studied conjugates 1–6. 相似文献
218.
Maurizio Sansotera Cristian Gambarotti Antonino Famulari Alberto Baggioli Raffaella Soave Francesco Venturini Stefano V. Meille Ivan Wlassics Walter Navarrini 《Tetrahedron》2014
Perfluoroalkyl radicals, generated by thermal decomposition of perfluorodiacyl peroxides, react selectively with quinone rings of 1,4-naphthoquinones. In the presence of a non-conjugated alkene such as 1-hexene, perfluoroalkyl radicals add to the double bonds of the olefin forming a radical adduct, which selectively adds to the naphthoquinone ring. Several perfluorodiacyl peroxides have been synthesized and used for the direct and alkene-mediated functionalization of naphthoquinones. Geometrical parameters and electron density topology of all perfluorodiacyl peroxides have been calculated by the density functional formalism and quantum theory of atoms in molecules to attempt a rationalization of the experimental reactivity. 相似文献
219.
Enantiomeric distribution of major chiral volatile organic compounds in juniper‐flavored distillates
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The enantiomeric ratios of chiral volatile organic compounds in juniper‐flavored spirits produced by various processing technologies in different EU countries were determined by multidimensional GC using solid‐phase microextraction and liquid–liquid extraction as a sample pretreatment procedure. In total, more than 260 compounds were detected in studied spirits from which linalool, α‐terpineol, 4‐terpineol, linalool oxides, α‐pinene, and verbenone were selected for enantiomeric separation. The significant differences in enantiomeric ratio of linalool and cis‐linalool oxide allowed us to distinguish between samples produced in Slovakia and the United Kingdom from those produced in Germany, Czech Republic, and Belgium. The pure enantiomer of trans‐linalool oxide was found only in samples from Germany. It was shown that the enantiomeric ratio is independent of the sample treatment procedure, and only small differences up to 1% were observed. 相似文献
220.
Ivan N. Derbenev James Dowden Jamie Twycross Jonathan D. Hirst 《Current Opinion in Green and Sustainable Chemistry》2022
In this review, we consider green chemistry metrics, related software tools, and the opportunities and challenges for their use in research laboratories. We provide an overview of state-of-the-art software designed both to aid researchers in planning and conducting chemical experiments and to assess sustainability of individual reactions and synthetic routes. The increasing digitalisation of research means that there is great opportunity for more extensive use of computational tools by synthetic chemists and for closer integration of green chemistry principles into the routine work of chemical laboratories. We discuss the scope for using software tools in the laboratory and assisting synthetic chemists in the adoption of green and sustainable chemistry approaches that are suitable for their specific purposes. 相似文献