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排序方式: 共有103条查询结果,搜索用时 15 毫秒
1.
The thermolysis of dicarbonylcyclopentadienyliron dimer in a sealed tube at 300°C has been reported to produce ferrocene, carbon monoxide, carbon dioxide, cyclopentadiene and elemental iron. We observe in addition to these products the production of biferrocene and elemental carbon. Thermolysis of carbonylcyclopentadienyliron tetramer (produced from the dimer by thermolysis in refluxing xylene) produces ferrocene, iron and carbon monoxidre; no biferrocene, carbon dioxide or elemental carbon are produced. A scheme is proposed to account for these products. 相似文献
2.
Thitivat Suebsaeng Charles A. Wilkie Vern T. Burger Janet Carter Charles Eric Brown 《Journal of polymer science. Part A, Polymer chemistry》1984,22(4):945-957
The solid reaction products from pyrolysis of polyethylene terephthalate in the presence and absence of red phosphorus were characterized by CP/MAS 13C-NMR, FR-IR, and MAS 31P-NMR spectroscopy. Over the temperature range of 300–400°C, polyethylene terephthalate was converted in a sealed vial to a highly crosslinked polymer of terephthalic acid. Pyrolysis in the presence of red phosphorus, which functions as a flame retardant by increasing the amount of char, yielded an intractible polyaromatic phosphate ester. After thermal cleavage of polyethylene terephthalate with formation of free carboxyl and vinyl ester groups, there are two competing reaction pathways. The smaller molecular weight fragments may enter the vapor phase where they undergo further degradation primarily to CO2, CO, and acetaldehyde, as described by others. However, if volatilization of the oligomeric fragments is inhibited, an alternate reaction pathway gives rise to the formation of highly crosslinked char. Red phosphorus decreases the volatility of the oligomeric fragments by converting them to phosphates and thereby enhances char formation. 相似文献
3.
Donald R. Dimmel Charles A. Wilkie Paul J. Lamothe 《Journal of mass spectrometry : JMS》1975,10(1):18-25
The mass spectra of (Me3Sn)nCH4?n, where n varies from 1 to 4, (Me3Sn)2CClX, where X equals H, Cl, Br or I, together with some tetraalkyltin compounds and Me3SnCCl3, are presented. Comparisons with mass spectra of the silicon analogs1 show a large number of similarities, including the appearance of allylic ions which require Group IV metal to carbon π-bonding. Multiple rearrangements are observed with the halogenated tin compounds which bring the α-halogen into direct bonding with the tin atom. 相似文献
4.
Direct observations of infrared absorption in the weakly bound dimer of carbonyl sulphide, produced in pulsed molecular beams, have been made. Diode laser spectra in the 5 micron, carbonyl stretching, wavelength region were recorded with FWHM linewidths of approximately 100 MHz. All of the observations are consistent with OCS dimer having a C 2h , centrosymmetric geometry, with the centres of mass of the monomers nearly opposite one another. This essentially perpendicular structure places the S atoms close to the centre of the complex. The perpendicular distance between the monomer axes is 3·64 Å. Intermolecular potential functions containing dispersion and electrostatic contributions are discussed. 相似文献
5.
α‐zirconium phosphate (ZrP) (prepared by both reflux and hydrothermal methods) is silylated with chlorotrimethylsilane and characterized by X‐ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy. Polystyrene/silylated‐ZrP composites show higher thermal stability as the ZrP content increases. Cone calorimetry suggests that the reduction of the peak heat release rate of polystyrene (PS)/ZrP composites does not increase as the ZrP loading increases; the aspect ratio of ZrP has little effect in fire performance of PS/ZrP composites. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
6.
Jayakody A. Chandrasiri Charles A. Wilkie 《Journal of polymer science. Part A, Polymer chemistry》1996,34(6):1113-1120
The graft copolymerization of acrylic acid onto acrylonitrile-butadiene-styrene terpolymer (ABS), has been initiated by the use of both benzoyl peroxide and azobisisobutyronitrile. Addition occurs in the butadiene region of the polymer, either by the loss of a vinylic hydrogen and subsequent radical formation and addition of monomer or by addition to the double bond. The amount of acrylic acid which may be added is dependent upon the time and temperature of the reaction and the concentration of monomer and initiator. Thermal analysis of the grafted samples show that the residue is less than that expected based upon the composition of the copolymer; similar results have been previously obtained for acrylic acid grafted by another technique. © 1996 John Wiley & Sons, Inc. 相似文献
7.
Variation of anions in layered double hydroxides: Effects on dispersion and fire properties 总被引:1,自引:0,他引:1
Layered double hydroxides (LDHs) are interesting materials for nanocomposite formation because one can vary the identity of the metals, the anions and the stoichiometry to see the effect of these on the ability of the nano-material to disperse in a polymer and to see what effect dispersion has on the properties of the polymer. In this study, the anions 2-ethylhexyl sulfate (SEHS), bis(2-ethylhexyl) phosphate (HDEHP) and dodecyl benzenesulfonate (SDBS) have been utilized as the charge balancing anions to synthesize organo-LDHs. Nanocomposites of poly(methyl methacrylate) (PMMA) and polystyrene (PS) with organo-LDHs were prepared both by melt blending and bulk polymerization. X-ray diffraction and transmission electron microscopy were used to characterize the morphology of the nanocomposites while the thermal stability and fire properties of nanocomposites were studied by thermogravimetric analysis and cone calorimetry; the mechanical properties are also investigated. In general, it is easier to disperse these organo-LDHs in PMMA than in PS, but the sulfate cannot be dispersed at the nanometer level in either material. The addition of these organo-LDHs does not affect the mechanical properties. The best fire properties are obtained with the sulfonate LDH, SDBS; the reduction in the peak heat release rate is almost 50% for both polymers. 相似文献
8.
Charles Eric Brown Charles A. Wilkie Jeffrey Smukalla Robert B. Cody James A. Kinsinger 《Journal of polymer science. Part A, Polymer chemistry》1986,24(6):1297-1311
The reaction of red phosphorus with poly(methyl methacrylate) under pyrolysis conditions was investigated with a number of physical techniques. A random methyl methacrylate/cyclic anhydride copolymer is formed from atatic PMMA, whereas a random methyl methacrylate/methacrylic acid copolymer is obtained with isotactic PMMA. The backbones of both these copolymers are more stable toward depolymerization than that of PMMA. The flame-retardant activity of red phosphorus with PMMA may arise in part from stabilization of the polymer toward depolymerization via modification of the sidechains. 相似文献
9.
Previous work has shown that -disubstituted (acac)2 titanium (IV) complexes exist in solution as nonrigid molecules [1]. These studies were followed by variable temperature 1H NMR spectroscopy. The spectra shows that for the dialkoxy and dihalo complexes the acetylacetonate (acac) rings exchange the methyl groups between the two nonequivalent sites of the cis isomer. These rearrangements take place an intramolecular rearrangement: both twisting and one bond rupture mechanisms have been suggested for these stero-chemical rearrangements [2-4]. 相似文献
10.
Hongdian Lu Charles A. Wilkie Ming DingLei Song 《Polymer Degradation and Stability》2011,96(5):885-891
Nanocomposites of poly (vinyl alcohol) with ethylamine modified zirconium phosphate (ZrP-EA) were prepared by solution blending. Their morphologies were elucidated with X-ray diffraction and transmission electron microscopy, while the thermal stability and flammability performance were characterized by thermogravimetric analysis, Fourier transform infrared spectra and microscale combustion calorimetry. It was established that the morphology of the nanocomposites evolved as ZrP-EA content increased. In the nanocomposites, catalytic degradation of the acetate groups remaining in poly (vinyl alcohol) occurred and catalytic carbonization was observed. Microscale combustion calorimetry revealed that the flammability performance of poly (vinyl alcohol) was improved by the introduction of zirconium phosphate nanoplatelets. 相似文献