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11.
Athar Ata Joe Ackerman Abdelhamid Bayoud Parvataneni Radhika 《Helvetica chimica acta》2004,87(3):592-597
From the methanolic extract of Cladiella sp., collected from the Andaman Island, India, a new sesquiterpene, cladidiol ( 2 ), and three known diterpenes, cladiellaperoxide ( 3 ), (6E)‐2α,9α‐epoxyeunicella‐6,11(12)‐dien‐3β‐ol ( 4 ), and polyanthellin A ( 5 ) were isolated. The structures of these compounds were established by extensive spectroscopic studies. Compound 2 exhibited modest acetylcholinesterase‐inhibition activity, and compounds 3 – 5 showed antibacterial activities against Streptococcus pyogenes, Escherichia coli, and Pseudomonas aeruginosa. 相似文献
12.
Nowduri Annapurna Adari Kalyan Kumar Parvataneni Vani Gollapalli Nageswara Rao 《Transition Metal Chemistry》2008,33(6):691-696
The kinetics of oxidation of l-cystine by MnIII have been studied in sulfuric acid medium at 30 °C. The reaction was followed spectrophotometrically at λmax = 500 nm. The
reaction shows first order dependence on both [MnIII] and [cystine]. It was found that the rate of the reaction decreases with increase of [H+] up to a certain point and then remains unchanged. The oxidation product of the reaction was found to be cysteic acid. A
plausible mechanism has been proposed to account for the experimental results. 相似文献
13.
The notion of a split coloring of a complete graph was introduced by Erd?s and Gyárfás [ 7 ] as a generalization of split graphs. In this work, we offer an alternate interpretation by comparing such a coloring to the classical Ramsey coloring problem via a two‐round game played against an adversary. We show that the techniques used and bounds obtained on the extremal (r,m)‐split coloring problem of [ 7 ] are closer in nature to the Turán theory of graphs rather than Ramsey theory. We extend the notion of these colorings to hypergraphs and provide bounds and some exact results. © 2002 Wiley Periodicals, Inc. J Graph Theory 40: 226–237, 2002 相似文献
14.
Nor Aiyyuhal Jemali Hasan Abu Kassim V. Radhika Devi Keshav N. Shrivastava 《Journal of Non》2008,354(15-16):1744-1750
We have used the density functional theory to make the models of GexSe1?x glass for which the energy is a minimum. The clusters, Ge2Se2, Ge2Se3, Ge3Se, Ge3Se2, Ge4Se, GeSe3, GeSe4, chain mode zig-zag Ge4Se3, corner sharing GeSe4, and edge sharing Ge2Se6, have been made successfully and their vibrational spectra have been calculated from the first principles. We are able to optimize the bond distances as well as the bond angles. The calculated values of the frequencies of vibrations of the various clusters have been compared with those obtained from the experimental Raman spectra of actual glasses, GexSe1?x(0 < x < 0.3). The local concentration, x within 0.25 nm is nonuniform in the amorphous material. When the same cluster occurs in two stable configurations, low frequency vibrations of frequency, ν < 100 cm?1, are found. The corner sharing GeSe4 has low frequency modes at 54 cm?1 and 93 cm?1 whereas these modes disappear in the pyramidal configuration. The low frequency modes are therefore associated with the breaking of C4 symmetry of the pyramidal configuration. The computed vibrational frequencies of clusters Ge3, Ge4Se3, Ge2Se3, GeSe3 and Ge3Se2 are actually present in the Raman spectra of the glass, GexSe1?x(0 < x < 0.3). 相似文献
15.
Russian Journal of Organic Chemistry - The present work describes the synthesis of 4-amino-6-(2-benzylidenehydrazinyl)-pyrimidine-5-carbonitrile derivatives,... 相似文献
16.
Glycolic acid was polymerized under vacuum in the presence and absence of nano sized clay.The added clay catalyzed the condensation polymerization which can be confirmed by recording FTIR spectroscopy and intrinsic viscosity (Ⅳ)values.The relative intensity of C=O/CH is increased while increasing the amount of clay.DSC showed the appearance of multiple endotherms of poly(glycolic acid).TGA showed the percentage weight residue remain above 750℃for polymer-nano composite system was 21% and hence proved the... 相似文献
17.
Ioannis Papanastasiou Andrew Tsotinis George B. Foscolos S. Radhika Prathalingam John M. Kelly 《Journal of heterocyclic chemistry》2008,45(5):1401-1406
18.
Self‐Assembly of “Chalcone” Type Push‐Pull Dye Molecules into Organic Single Crystalline Microribbons and Rigid Microrods for Vis/NIR Range Photonic Cavity Applications
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Radhika Vattikunta Dasari Venkatakrishnarao Prof. Dr. Mahamad Ahamad Mohiddon Prof. Dr. Rajadurai Chandrasekar 《Chemphyschem》2016,17(21):3435-3441
A novel supramolecular fluorescent donor–acceptor type dye molecule, (2E,4E)‐1‐(2‐hydroxyphenyl)‐5‐(pyren‐1‐yl)penta‐2,4‐dien‐1‐one (HPPD) self‐assembles in a mixture of ethanol/chloroform through intermolecular π–π stacking (distance ca. 3.384 Å) to form J‐aggregated single‐crystalline microribbons displaying Fabry–Pèrot (F‐P) type visible‐range optical resonance. The corresponding borondifluoride dye (HPPD‐BF), with a reduced HOMO–LUMO gap, self‐assembles into crystalline microrods acting as an F‐P type resonator in the near‐infrared (NIR) range. 相似文献
19.
Pervanadyl (VO2+) complexes with N‐(aroyl)‐N′‐(picolinylidene)hydrazines (HL = Hpabh, Hpath and Hpadh; H stands for the dissociable amide hydrogen) are described. The Schiff bases were obtained by condensation of 2‐pyridine‐carboxaldehyde with benzhydrazide (Hpabh), 4‐methylbenzhydrazide (Hpath) and 4‐dimethylaminobenzhydrazide (Hpadh), respectively. The reaction of [VO(acac)2] and HL in acetonitrile in air affords the complexes of general formula [VO2L]. The diamagnetic nature and EPR silence confirm the +5 oxidation state of vanadium in these complexes. Infrared spectra of the complexes are consistent with the enolate form of the coordinated ligands. Electronic spectra show charge transfer bands in the range 486–233 nm. The complexes are redox active and display an irreversible reduction (–0.64 to –0.72 V vs. Ag/AgCl). The crystal structures of all the complexes have been determined. In each complex, the metal centre is in a distorted trigonal‐bipyramidal N2O3 coordination sphere formed by the pyridine‐N, the imine‐N and the deprotonated amide‐O donor L– and two oxo groups. The planar ligand satisfies one equatorial and two axial positions. The other two equatorial positions are occupied by the two oxo groups. In the solid state, the molecules of each of the three complexes form a chain‐like arrangement via the azomethine‐H…oxo interactions. Interchain weak π‐π interactions lead to two dimensional networks for [VO2(pabh)] and [VO2(path)]. On the other hand, [VO2(padh)] forms a two‐dimensional network through interchain N‐methyl‐H…oxo interactions. 相似文献
20.