全文获取类型
收费全文 | 747篇 |
免费 | 28篇 |
国内免费 | 1篇 |
专业分类
化学 | 565篇 |
晶体学 | 2篇 |
力学 | 5篇 |
数学 | 85篇 |
物理学 | 119篇 |
出版年
2023年 | 4篇 |
2022年 | 9篇 |
2021年 | 13篇 |
2020年 | 22篇 |
2019年 | 22篇 |
2018年 | 12篇 |
2017年 | 7篇 |
2016年 | 28篇 |
2015年 | 21篇 |
2014年 | 28篇 |
2013年 | 44篇 |
2012年 | 60篇 |
2011年 | 57篇 |
2010年 | 19篇 |
2009年 | 30篇 |
2008年 | 52篇 |
2007年 | 49篇 |
2006年 | 35篇 |
2005年 | 48篇 |
2004年 | 35篇 |
2003年 | 29篇 |
2002年 | 25篇 |
2001年 | 5篇 |
2000年 | 8篇 |
1999年 | 11篇 |
1998年 | 5篇 |
1997年 | 10篇 |
1996年 | 6篇 |
1995年 | 9篇 |
1994年 | 9篇 |
1993年 | 6篇 |
1992年 | 4篇 |
1991年 | 4篇 |
1990年 | 5篇 |
1989年 | 3篇 |
1987年 | 2篇 |
1985年 | 4篇 |
1984年 | 4篇 |
1981年 | 5篇 |
1980年 | 2篇 |
1978年 | 2篇 |
1977年 | 6篇 |
1976年 | 3篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1973年 | 4篇 |
1972年 | 1篇 |
1971年 | 1篇 |
1933年 | 1篇 |
1910年 | 1篇 |
排序方式: 共有776条查询结果,搜索用时 15 毫秒
1.
2.
Indrajit Lahiri 《Journal of Mathematical Analysis and Applications》2002,271(1):206-216
In this paper we prove a uniqueness theorem for meromorphic functions sharing three values with some weight which improves some known results. 相似文献
3.
4.
Dipak Ghosh Madhumita Lahiri Argha Deb Susobhan Das Krishnadas Purkait Biswanath Biswas Jayanta Roy Choudhury Rini Chatterjee Abdul Kayum Jafry 《Zeitschrift fur Physik C Particles and Fields》1996,71(1):243-249
The scaled factorial moments and the multifractal moments have been investigated in differentη-intervals to study the dynamical fluctuation of pions produced in 200 AGeV32S-Ag/Br interaction. In order to investigate the detail characteristics of intermittency behaviour, theF-moments are extracted up to the eighth order of moments in differentM-intervals. The analysis indicates a non-thermal phase transition and different regime of particle production during the hadronisation process. 相似文献
5.
Himadri Paul Sumit Bhaduri Goutam Kumar Lahiri 《Journal of organometallic chemistry》2004,689(2):309-316
Fumed silica, silica gel, silica-alumina and cross-linked (5.5%) polystyrene have been functionalized with quaternary ammonium groups and the Chini cluster [Pt12(CO)24]2− has been anchored onto these functionalized materials by ion pairing. A catalyst has also been prepared by the adsorption of Na2[Pt12(CO)24] on unfunctionalized fumed silica. The catalytic activities of the resultant materials, and that of commercially purchased 5% platinum on alumina have been studied for the hydrogenation of a variety of unsaturated compounds. The substrates studied are: α-acetamidocinnamic acid, cyclohexanone, acetophenone, methyl pyruvate, ethyl acetoacetate, nitrobenzene and benzonitrile. Compared to the polystyrene supported catalyst, the inorganic oxide supported catalysts have higher surface areas and for most of the substrates have notably higher activities. The functionalized fumed silica-based catalyst gives higher conversions than functionalized silica gel and silica-alumina-based catalysts. In the hydrogenation of acetophenone and ethyl acetoacetate, the functionalized fumed silica-based catalyst show superior activity compared to the commercial platinum catalyst, and the catalyst made by conventional adsorption method. In benzonitrile hydrogenation with all the cluster-derived catalysts a hydrazine derivative is selectively formed, but when the commercial platinum catalyst is used benzyl amine is the main product. 相似文献
6.
Summary Studies on adsorption behavior of heavy radionuclides, present altogether in no-carrier-added state, e.g., 197-200Pb, 197-200Tl and 197Hg, have been carried out with calcium alginate beads. High lead (100%) and moderate thallium removal (~65%) was achieved
in pH range 2-7. 100% mercury removal was also achieved at pH 2 and 4. Effort has been made to recover all three radionuclides
adsorbed in the calcium alginate beads using various chemicals, such as HCl, thiourea, sodium acetate, sodium oxalate and
sodium nitrite. It was found that 0.1M HCl and 0.1M thiourea could remove at pH 1 80-90% of adsorbed Pb. Tl recovery was possible
by all chemicals mentioned above. Hg was also recovered by all chemicals except HCl. 相似文献
7.
Kar S Chanda N Mobin SM Urbanos FA Niemeyer M Puranik VG Jimenez-Aparicio R Lahiri GK 《Inorganic chemistry》2005,44(5):1571-1579
The reaction of cis-Ru(acac)2(CH3CN)2 (acac = acetylacetonate) with 2,2'-dipyridylamine (L) in ethanolic medium resulted in facile one-pot synthesis of stable [(acac)2RuIII(L)]ClO4 ([1]ClO4), trans-[(acac)2RuII(L)2] (2), trans-[(acac)2RuIII)L)2]ClO4 ([2]ClO4), and cis-[(acac)2RuII(L)2] (3). The bivalent congener 1 was generated via electrochemical reduction of [1]ClO4. Although in [1]+ the dipyridylamine ligand (L) is bonded to the metal ion in usual bidentate fashion, in 2/[2]+ and 3, the unusual monodentate binding mode of L has been preferentially stabilized. Moreover, in 2/[2]+ and 3, two such monodentate L's have been oriented in the trans- and cis-configurations, respectively. The binding mode of L and the isomeric geometries of the complexes were established by their single-crystal X-ray structures. The redox stability of the Ru(II) state follows the order 1 < 2 < 3. In contrast to the magnetic moment obtained for [1]ClO4, mu = 1.84 muB at 298 K, typical for low-spin Ru(III) species, the compound [2]ClO4 exhibited an anomalous magnetic moment of 2.71 muB at 300 K in the solid state. The variable-temperature magnetic measurements showed a pronounced decrease of the magnetic moment with the temperature, and that dropped to 1.59 muB at 3 K. The experimental data can be fitted satisfactorily using eq 2 that considered nonquenched spin-orbit coupling and Weiss constant in addition to the temperature-independent paramagnetism. [1]ClO4 and [2]ClO4 displayed rhombic and axial EPR spectra, respectively, in both the solid and the solution states at 77 K. 相似文献
8.
Yu Yang Maya Belghazi Arnaud Lagadec David J. Miller Steven B. Hawthorne 《Journal of chromatography. A》1998,810(1-2):149-159
The intermolecular interactions between organic solutes and sorbent matrices under subcritical water conditions have been investigated at a pressure of 50 bar and temperatures ranging from 50 to 250°C. Both polar and nonpolar organics (chlorophenols, amines, n-alkanes, and polycyclic aromatic hydrocarbons) and five different sorbent matrices (glass beads, alumina, Florisil, silica-bonded C18, and polymeric XAD-4 resins) were used. From the same matrix, the polar solutes always eluted at lower temperatures, while the moderately polar and nonpolar solutes only eluted at higher temperatures. Similar to matrix effects previously observed using supercritical carbon dioxide, the sorbent type greatly influenced the elution efficiency under subcritical water conditions. Lower temperatures are sufficient to elute a particular solute from glass beads, alumina, and Florisil, but higher temperatures (less polar water) are needed to elute the same solute from silica-bonded C18. The highest temperatures were required to elute aromatic organics from XAD-4. These matrix effects demonstrate that, while low temperature water can break inert or dipole interactions between solutes and glass beads, alumina, and Florisil, higher temperature water is required to interrupt the van der Waals attractions between solutes and silica-bonded C18, and even higher temperatures needed to overcome the π-electron interactions between aromatic solutes and XAD-4. 相似文献
9.
The reaction of cycloheptatriene (CHT) with dibenzoylacetylene (DBA), in refluxing toluene gave a mixture of products consisting of 6,7-dibenzoyltricyclo[3.2.2.02.4]nona-6,8-diene 6 and 3,4-dibenzoylbicyclo [3.2.2]nona-2,6,8-triene 7. Neat heating of a mixture of CHT and DBA around 95–100° gave besides, 6 and 7, small amounts of two dimers of DBA. Photolysis of 6 in benzene solution gave a lactonic, rearrangement product. 25. The structures of the various products have been established and reasonable mechanisms for their formation have been suggested. 相似文献
10.
Irina G. Gazaryan Maya Yu. Rubtsova Yuri L. Kapeliuch José Neptuno Rodriguez-Lopez L. Mark Lagrimini Roger N. F. Thorneley 《Photochemistry and photobiology》1998,67(1):106-110
The properties of a newly isolated anionic tobacco peroxidase from transgenic tobacco plants overexpressing the enzyme have been studied with respect to the chemiluminescent reaction of luminol oxidation. These were compared to the properties of horseradish peroxidase in the cooxidation of luminol and p -iodophenol, the enhanced chemiluminescence reaction. The pH, luminol and hydrogen peroxide concentrations were optimized for maximum sensitivity using the tobacco enzyme. The detection limit for the latter under the optimal conditions (2.5 m M luminol, 2 m M hydrogen peroxide, 100 m M Naborate buffer, pH 9.3) was about 0.1 p M , which is at least five times lower than that for horseradish peroxidase in enhanced chemiluminescence with p -iodophenol. The rate constants for the elementary steps of the enzyme-catalyzed reaction have been determined: k 1 = 4.9 × 106 M −1 s1 , k 2 = 7.3 × 106 M −1 s−1 , k 3 = 2.1 × 106 M −1 s−1 (pH 9.3). The similarity of these rate constants is unusual for plant peroxidases. The high catalytic activity of tobacco peroxidase in the luminescent reaction is explained by the high reactivity of its Compound II toward luminol and the high stability of the holoenzyme with respect to heme dissociation. This seems to be a unique property of this particular enzyme among other plant peroxidases. 相似文献