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  • 1995-1999  (141)
  • 1985-1989
  • 1870-1879
  • 1998  (141)
  • Industrial Chemistry and Chemical Engineering  (141)
Materialart
Erscheinungszeitraum
  • 1995-1999  (141)
  • 1985-1989
  • 1870-1879
Jahr
  • 101
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 155-160 
    ISSN: 0268-2605
    Schlagwort(e): tungsten trioxide ; electrochromism ; thin films ; chemical vapor deposition (CVD) ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Crystalline and amorphous thin films of tungsten(VI) oxide can be prepared by chemical vapor deposition using a variety of volatile precursors below 500 °C. Deposition parameters for preparation of WO3 films from tungsten hexacarbonyl [W(CO)6], tungsten hexafluoride (WF6), tungsten ethoxides [W(OEt)x, x = 5, 6] and tetra(allyl)tungsten [W(η3-C3H5)4] are summarized. The electrochromic behavior of these films is comparable with that observed for WO3 films prepared by evaporation, sputtering and electrodeposition. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 102
    ISSN: 0268-2605
    Schlagwort(e): chemical vapor deposition ; platinum ; palladium ; rhodium ; heterogeneous catalysts ; fluidized bed ; MOCVD ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new one-step method, entitled fluidized-bed metal-organic chemical vapor deposition (FBMOCVD) of preparing highly dispersed metal-supported catalysts is reported. The following complexes were studied and used as CVD precursors in presence of H2: [Rh(μ-Cl)(CO)2]2, Rh(allyl)3, Rh(acac)(CO)2, Pd(allyl)(hfac), Pd(allyl)(Cp), Pt(COD)(CH3)2. (acac, acetylacetonato; hfac, hexafluoroacetylacetonato; Cp, cyclopentadienyl; COD, cyclooctadienyl). In a first approach, depositions on planar substrates were carried out to establish the best experimental conditions to obtain good-quality deposits. X-ray diffraction, X-ray photo-electron spectroscopy and electron microprobe studies were realized on the resulting thin films. Analyses of the products contained in the gas phase after and during deposition were performed by mass spectrometry and GC-MS. Finally, catalysts prepared by FBMOCVD were characterized by transmission electron microscopy-energy dispersion spectroscopy (TEM-EDS), metal-loading determinations and specific-surface measurements (BET). Dispersed nanosized aggregates were obtained, showing high activities in alkene hydrogenation and alcohol hydrocarbonylation. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 103
    ISSN: 0268-2605
    Schlagwort(e): Metal-organic chemical vapor deposition (MOCVD) ; precursors ; titanium ; vanadium ; carbonitride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ceramic thin films containing titanium, vanadium, carbon, oxygen and nitrogen were obtained on steel substrates at 873 K, under nitrogen and helium gases and at low pressure, by chemical vapor deposition (CVD) from two organometallic precursors, CpTiCl2N(SiMe3)2 and Cp2VMe2 (Cp, cyclopentadienyl). Independent TG-DTA-MS and CVD studies of the two precursors showed their ability to co-decompose within compatible temperature and pressure domains. The mechanism of the reactions occurring inside the CVD apparatus was also approached by GC-MS and NMR analyses of the condensed decomposition products. CVD conducted under He gas confirmed that the formation of nitride resulted from the nitrogen atoms of the precursor, but the nitrogen content in the films remained lower than approx. 5%. Higher nitrogen contents (up to 12%) were only obtained when using ammonia as a carrier gas. Both precursors being air- and moisture-sensitive, high-purity CVD equipment was used to reduce oxycarbide formation. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 104
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 189-199 
    ISSN: 0268-2605
    Schlagwort(e): single-source precursor ; tetrakis(diethylamido)chromium ; pyrolysis mechanism ; MOCVD ; low-temperature deposition ; chromium carbonitride thin films ; hard metallurgical coatings ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Amorphous chromium carbonitride coatings with a low nitrogen content (3-8 at%) were deposited by low-pressure MOCVD in the temperature range 573-793 K using Cr(NEt2)4 as single-source precursor. This poor nitrogen incorporation is in agreement with the trends predicted by thermochemical calculations. XPS data, resistivity measurements and annealing experiments suggest that the films grown at 573 K are contaminated by organic species due to incomplete elimination of the ligands. The films deposited at higher temperature crystallize upon annealing at 873 K to form an orthorhombic ternary chromium carbonitride phase. The major volatile by-products of the MOCVD reaction were analyzed by 1H and 13C NMR. Their amount and the quasi-equimolar EtN=CHMe/HNEt2 ratio suggest that most of the NEt2 ligands are removed by a stepwise mechanism which probably occurs with other diethylamido complexes of transition metals when they are used as single-source precursors in MOCVD. The incorporation of the metalloid elements in the film is discussed in comparison with recent literature data. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 105
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 201-220 
    ISSN: 0268-2605
    Schlagwort(e): MOCVD ; molybdenum oxycarbide ; chromium oxycarbide ; coating ; kinetics ; microstructure ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A review of the coating kinetics of molybdenum and chromium oxycarbides and a study on the properties of deposited films are reported. Molybdenum carbonyl, chromium carbonyl and their mixture were used to prepare coatings at temperatures between 170 and 450 °C on SS304 or SiC substrates by a process of metal-organic chemical vapor deposition (MOCVD). The processing parameters of the coatings, such as the evaporation of precursors, coating pressure and temperature, are discussed along with the coating rates, compositions and other microstructural information, so to reveal the kinetics of the coating process on two different substrates. In addition, the chemical composition, crystalline phases and microstructure of the coatings obtained in various conditions are presented with the evidence interpreted by various electron-microscopic and spectroscopic techniques, including XRD, EDS, EPMA and XPS. The dependence of some properties, such as hardness, adhesive strength and corrosive resistance of the coatings on SS 304, on their composition and the deposited phases, i.e. as a function of coating temperature and pressure, is reviewed. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
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  • 106
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 221-236 
    ISSN: 0268-2605
    Schlagwort(e): MOCVD ; barium ; liquid delivery ; mixed-metal species ; aerosol-assisted CVD ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Conventional MOCVD techniques require molecules displaying volatility and constant vapor pressure. Metal oxide precursors, i.e., β-diketonates, or classical or functionalized metal alkoxides are mostly solids. The various approaches used to tailor volatility are discussed with barium derivatives as an example. The relationships between sublimation temperature and molecular weight suggest that volatility can be optimized on the basis of molecular weight.   Aerosol-assisted CVD (AACVD) can use a larger range of precursors since volatility is no longer crucial. The solvent is an undesired ballast in a CVD process. High solubility of the precursors in the selected solvent is thus desirable. ‘Stability’ here includes the absence of precipitation which would change the stoichiometry of the feed solution for multicomponent oxides. Precipitation is often promoted by hydrolysis; stability toward moisture is thus desirable. The use of mixtures of precursors based on different ligands (β-diketonates, β-ketoesterates, alkoxides) can lead to ligand exchange reactions giving homometallic species, sometimes of low solubility, or mixed-metal species by self-assembly, thus improving solubility and stability toward moisture. These aspects are illustrated in compositions related to high-Tc superconductors. Novel copper, yttrium, cerum(IV), barium-copper, yttrium-copper and praseodynium-copper species are reported. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 107
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 293-293 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 108
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 109
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 294-294 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 110
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 294-295 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 111
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 295-296 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 112
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 296-296 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 113
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 114
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 296-297 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 115
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 297-297 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 116
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 117
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 298-298 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 118
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 237-241 
    ISSN: 0268-2605
    Schlagwort(e): tin ; iodomethane ; solubilization ; methyltin species ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The dissolution of tin metal by iodomethane-water mixtures has been studied and the influence of several parameters on both the extent and rate of reaction investigated. The rate-determining step shows a pseudo-first-order dependence on iodomethane (CH3I). The reaction is strongly dependent upon both water and oxygen. The activation energy of only 16 kJ mol-1 is interpreted in terms of a facile bond-breaking and making process at the metal surface, generating methyltin species. Analysis by hydride generation and GC-AA confirmed the formation of methylated species ranging from monomethyl- to tetramethyl-tin; inorganic tin (from hydrolysis) was the major form, however. These findings are similar to those made earlier by us on the solubilization of arsenic from GaAs by alkyl halide-water mixtures, and a similar multi-step scheme is proposed. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 119
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 243-251 
    ISSN: 0268-2605
    Schlagwort(e): arsenic ; speciation ; algae ; Fucus gardneri ; arsenosugar ; high-performance liquid chromatography (HPLC) ; inductively coupled plasma-mass spectrometry (ICP-MS) ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Arsenic speciation in a brown alga, Fucus gardneri, collected in Vancouver, B.C., Canada, was carried out by using high-performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS). Hydride generation-atomic absorption spectrometry (HG-AAS) was used for total arsenic determination. The relative amounts of some arsenosugars 1 in growing tips are found to be different in comparison with the remainder of the plant. Fucus samples collected in summer contain 9 ppm of total arsenic. Most of the arsenic species are extractable. Fucus samples collected in winter contain relatively higher amounts of arsenic, 16-22 ppm, but only low amounts of this are extractable. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 120
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 253-256 
    ISSN: 0268-2605
    Schlagwort(e): disilane ; gas source MBE ; synchrotron radiation ; silicon hydride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Surface hydrogen and growth mechanisms are investigated for synchrotron radiation (SR)-assisted gas source molecular beam epitaxy (SR-GSMBE) using Si2H6 on the Si(100) surface in the low-temperature region. The surface silicon hydrides (deuterides) are monitored in situ during the epitaxial growth by means of infrared reflection absorption spectroscopy with a Si(100) substrate and a CoSi2 buried metal layer. It is concluded that the chemisorption of gas-phase reactive species such as SiHn and H generated by SR irradiation and the subsequent hydrogen desorption are the key mechanisms of SR-GSMBE at low substrate temperatures. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 121
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 257-264 
    ISSN: 0268-2605
    Schlagwort(e): Rochow reaction ; cesium chloride ; rubidium chloride ; silicon impurities ; action of promoters ; scanning electron microscopy (SEM) ; energy-dispersive X-ray spectroscopy (EDX) ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cesium chloride- and rubidium chloride-promoted Rochow contact masses based on both technical-grade and highly pure silicon have been investigated in the Rochow reaction and by REM/EDX surface analysis. The alkali-salt promoters seem to act analogously to the well-known zinc promoter, by localizing the reaction to distinct reactive areas and keeping free the surface area for the reaction, probably for the formation of catalytically active Cu-Si surface species. The alkali salts exhibited their promoting action only in combination with the impurities within the technical-grade silicon. Otherwise, they acted as blocking poisons. The promoter action of alkali chlorides in contact masses based on technical-grade silicon is possibly connected with the formation of salt melts, containing alkali chlorides and impurities. These melts, analogously to zinc chloride, could dissolve oxidic impurities from the silicon surface which otherwise would enhance the blocking of potentially active surface by extensive copper deposition. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 122
    ISSN: 0268-2605
    Schlagwort(e): carbohydrate surfactants ; wetting behaviour ; siloxane ; silane ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The wetting behaviour of carbohydrate surfactants bearing siloxane, carbosilane, polysilane or silane moieties has been investigated. By static surface tension (γlv, σ) and wetting tension (γsv-γsl, α) measurements on a non-polar perfluorinated surface (FEP®), the contact angles of aqueous surfactant solutions above the critical micelle formation concentration (cmc) were determined. Surface tension and wetting tension react independently on defined changes in the chemical structure of the surfactant molecules. Siloxane surfactants reduce the surface tension most effectively, whereas for a neopentyl-substituted silane derivative the lowest solid/liquid interfacial tension was found. The data for isomeric siloxanes, carbosilanes and silanes suggest that donor-acceptor forces at solid interfaces have a maximum range of about 4.5 Å. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 123
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 277-284 
    ISSN: 0268-2605
    Schlagwort(e): carboxylation ; methane ; carbon monoxide ; ytterbium(III) acetate ; manganese(II) acetate ; sodium hypochlorite ; acetic acid ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new method of synthesis of acetic acid in water has been developed from the carboxylation of methane with carbon monoxide using lanthanide catalysts. Ytterbium(III) acetate has been found to be the most active catalyst among the compounds of the lanthanide series in the carboxylation reaction of methane with carbon monoxide. Sodium hypochlorite or hydrogen peroxide was used as the oxidant in this reaction. Sodium hypochlorite exhibited more favorable activity than hydrogen peroxide in the reaction. The catalytic activity was improved by the addition of transition-metal salts such as manganese(II) acetate. The best result has been found at a ratio of manganese(II) acetate to ytterbium(III) acetate of 1:10. The optimum reaction conditions (reaction temperature, 40 °C; time, 20 h; methane, 20 atm; carbon monoxide, 5 atm) have been obtained. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 124
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 298-299 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 125
    ISSN: 0268-2605
    Schlagwort(e): Nickel-σ-organyl complexes ; dispersed atomic Ni(0) ; Ni(I) ions ; silica ; EPR ; FMR ; spectrum calculation ; strain ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dispersed atomic nickel(0) is formed during the reaction of the nickel-σ-organyl complexes with silanol groups at temperatures below 373 K. That nickel is oxidized to Ni(I) by protons of the silanol groups in a consecutive step. The Ni(I) portion amounts to about 70% w/w of the Ni used. Six different Ni(I) species are detected by electron paramagnetic resonance. They are stabilized by interaction with the silica surface and the organic moieties; they act as anchor ions for the Ni(0) atoms. Ni(0) crystallites stabilized in this way are about 0.5 nm in diameter after a treatment at 373 K. The influence of the Ni(I) ions on the collective, magnetic properties of the clusters is revealed by calculation of ferromagnetic resonance (FMR) spectra using the independent-grain approach according to Schlömann and Kotyukov. A strain of about 10 GPa is brought about in the nickel crystallites by the interaction with Ni(I) ions. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 126
    ISSN: 0268-2605
    Schlagwort(e): magnetization reversal ; iron oxide particles ; SQUID ; atomic force microscopy ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We report first measurements of the magnetization reversal of monodisperse 30 nm and 50 nm ferromagnetic Fe3O4 particles. These particles are produced in a carrier gas as an aerosol by spray pyrolysis. After production and size selection, they are precipitated on a silicon chip with a niobium SQUID (superconducting quantum interference device) incorporated on its surface. By changing a magnetic field in the plane of the SQUID, we can measure the magnetization reversal of the particles by the flux they induce into the SQUID. The angular dependence of this reversal is determined by rotating the magnetic field around the SQUID. Scanning electron microscope (SEM) images have confirmed the particle size and revealed the position of the collected particles. If the particle concentration is too high, we cannot detect changes in the magnetic moment of a single particle, but measure the magnetic properties of the whole assembly. If only a few particles are found on the SQUID loop the angular dependence of the magnetic reversal of a single particle can be measured; this result is compared with a simple model of magnetization reversal. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 127
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 337-340 
    ISSN: 0268-2605
    Schlagwort(e): porous silicon ; luminescence ; light-assisted etching ; atomic force microscopy ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We present an investigation into a new technique for producing luminescent porous silicon with controlled lateral microstructure. The process is based on the effect of laser-assisted stain etching of silicon with hydrofluoric acid solution. With the further goal of preparing two-dimensional periodical arrays of luminescent microdots, we studied the accuracy of the technique by etching single submillimetre structures with a low-power laser. The size and exact position of the etched area are controlled by laser focusing and movement, respectively, with submillimetre accuracy. Samples exhibit orange luminescence when illuminated with UV or blue light.We have studied the dependence of the efficiency of the luminescence, the structure and the rate of etching on parameters such as the HF concentration, the intensity and wavelength of illumination and the doping level of the silicon wafer. Optimization of the process parameters, and consistency with assumed mechanisms of luminescence and etching process, are discussed. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 128
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 341-346 
    ISSN: 0268-2605
    Schlagwort(e): silver halides ; nanoparticles ; pseudoisocyanine ; stability ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Pseudoisocyanine (PIC) was adsorbed on colloidal silver halide nanoparticles where it formed aggregates (J-aggregates). The nanoparticles were prepared using a surfactant (AOT)/n-heptane/water microemulsion. The molecules of pseudoisocyanine replaced the molecules of surfactant (AOT) on the surface of the nanoparticles and caused an instability of the silver bromide dispersion. The stability could be improved by two methods: either by using an adsorption inhibitor (e.g. p-xylene) or by adding another surfactant (CTAB). The adsorption has also been carried out at low temperature: the stability of the particles was then improved, and the J-aggregates are smaller. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 9 Ill.
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  • 129
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 387-391 
    ISSN: 0268-2605
    Schlagwort(e): colloidal manganese ; ESR ; susceptibility ; antiferromagnetism ; superparamagnetism ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reduction of MnBr2·2THF (THF = tetrahydrofuran) using K[BEt3H] yields the organosol [Mn·0.3THF]x. According to the UV/Vis, ESR (electron spin resonance spectroscopy), HRTEM (high-resolution transmission electron microscopy), XPS (X-ray photoelectron spectroscopy) and XAS (X-ray absorption spectroscopy) data, this nanosized metal colloid consists of small THF-stabilized Mn0 particles which show, in susceptibility investigations, a diminished magnetic coupling as deduced from the Weiss temperature, Θ = 96 K. The Neél temperature TN is likewise strongly reduced in comparison with the bulk value (95 K). The THF-stabilized Mn0 particles exhibit superparamagnetism below 20 K, with a partial blocking at 10 K, and to our knowledge represent the first colloid consisting of particles of an elemental antiferromagnetic metal. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 6 Ill.
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  • 130
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 305-314 
    ISSN: 0268-2605
    Schlagwort(e): mesoporous ; oxides ; nanostructures ; luminescence ; zeolites ; guest/host ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ordered porous inorganic compounds can now be synthesized with pore sizes between 0.3 nm and several tens of nanometers. The sharp pore size distribution of such materials and the ordered pore arrangement open possibilities for using them to organize matter on the nanometer scale. This overview highlights different aspects of this topic, using four selected examples: the spatial organization of molecules with high molecular hyperpolarizability to create a frequency-doubling element; the encapsulation of a laser dye which results in a new class of solid-state lasers; the encapsulation of small metal clusters in mesoporous ordered oxides; and the encapsulation of semiconductor clusters in such oxides. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 131
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 401-408 
    ISSN: 0268-2605
    Schlagwort(e): Metallocene ; Ziegler-Natta ; Polypropylene ; α-Olefins ; Catalysis ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The polymerization of propylene using a mixture of racemic metallocenes and Ziegler-Natta catalysts was investigated. The polypropylene was obtained as a mixture of a fine powder and beads, with the powder being absorbed partially on the beads. The relative amount of the powder can be controlled by the concentration of the metallocene. The compatibility between the components of the mixed catalytic systems and the effect of the components on the rate of polymerization and on the properties of the new polymers were studied. The metallocene system dramatically affects the melt viscosity, isotacticity and molecular weight of the polymers. The two catalytic systems are able to act jointly, producing different polymers, for which separate melting and crystallization temperatures are obtained. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 132
    ISSN: 0268-2605
    Schlagwort(e): density functional calculation ; binuclear metal carbonyl ; Cr2(CO)6+ ; laser ablation ; molecular beam ; optimized structures ; dissociation energy ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Density functional calculations have been made on a binuclear metal carbonyl ion Cr2(CO)6+ found in our laser ablation-molecular beam (LAMB) experiment. Optimized structures are calculated for three different conformations: T33 of D3d symmetry with three terminal carbonyl groups on each chromium atom, B2T22 of D2h symmetry with two bridging carbonyl groups and two terminal carbonyl groups on each chromium atom, and B4T11 of D4h symmetry with four bridging carbonyl groups and one terminal carbonyl group on each chromium atom. The most stable conformation is T33 which is 36.76 and 286.44 kJ mol-1 lower in energy than B2T22 and B4T11, respectively. The difference of conformation exerts a significant influence on the internuclear distance between chromium and the carbon of terminal CO, but hardly on the Cr-Cr bond length. For B2T22 and B4T11, longer C-O distances for bridging carbonyls compared with those for terminal ones indicate effective π*-back donation from the chromium atom to the bridging carbonyl groups. Furthermore, the relative abundance of Cr2(CO)n+ (n = 0-6) observed in our previous experimental study can be explained qualitatively by comparison of the excess energy produced in the formation of a Cr+-Cr bond with the CO dissociation energy of Cr2(CO)6+. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 133
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 467-468 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 134
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 468-468 
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 135
    ISSN: 0268-2605
    Schlagwort(e): Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 136
    ISSN: 0268-2605
    Schlagwort(e): metal clusters ; quantum-size effect ; nanostructures ; size effects ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Meta-cluster compounds can be exploited advantageously to study the evolution, with increasing size of the molecules of the physical properties of metal clusters from molecular to bulk-metal behavior. The metal-cluster molecules are well-defined, stoichiometric, chemical compounds. The molecules consist of a metal core of a variable number of atoms, surrounded by a shell of ligand atoms or molecules. Depending on the compound, the type of metal atom may be varied, whereas the core size can be changed from a few up to several thousands of atoms. Accordingly, these materials provide excellent model systems for monodisperse metal particles, embedded in a dielectric matrix, and can be investigated by the well-known experimental techniques of solid-state physics. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 137
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 815-818 
    ISSN: 0268-2605
    Schlagwort(e): desilylation ; hydroxyquinones t-butyldimethylsilyl ethers ; potassium fluoride ; tetra-n-butylammonium fluoride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Desilylation of a series of hydrolytically stable hydroxyquinone t-butyldimethylsilyl ethers was achieved in high yields by the use of potassium fluoride in the presence of catalytic amounts of aqueous 48% hydrobromic acid (HBr), or basic aluminium oxide (Al2O3), and tetra-n-butylammonium fluoride (Bu4NF) as cleaving agents. Copyright © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 2 Tab.
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  • 138
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 541-549 
    ISSN: 0268-2605
    Schlagwort(e): organotin speciation ; analytical validation procedure ; organotin sediment extraction ; Grignard derivatization ; organotin extraction stability ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The effect of several extraction variables such as acid concentration and strength (e.g. for HCl and HOAc), the presence of complexing agents (e.g. tropolone, sodium diethyldithiocarbamate) in the extracting mixture, solvent polarity (e.g. hexane, toluene) and sonication time for native butyl- and phenyl-tin compounds from sediment was evaluated. A toluene-HOAc mixture (10:4) yields the highest extraction efficiency for all the analytes and minimizes the degradation of trialkyl- and triaryl-tins during the extraction under sonication. In addition, losses of underivatized monobutyltin and monophenyltin were minimized in several steps of the analytical procedure. The analytical procedure developed was validated against existing CRMs for butyltin determination. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 139
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 667-673 
    ISSN: 0268-2605
    Schlagwort(e): polysilanes ; poly(dimethylsiloxane) ; polyphosphazenes ; atom transfer radical polymerization ; controlled/‘living’ radical polymerization ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Recent advances in the synthesis of block, graft and star polymers containing inorganic macromolecular species are described. Anionic copolymerization techniques were used in the for-­mation of diblock copolymers of poly(styrene-block-methylphenylsilylene) and poly(isoprene-block-methylphenylsilylene) by the ring-opening polymerization of 1,2,3,4-tetramethyl-1,2,3,4-tetraphenylcyclotetrasilane initiated by living anionic polystyrene and isoprene respectively. Hydrosilation of an attachable initiator onto telechelic vinyl- or hydrosilyl-terminal or­-pendant poly(dimethylsiloxane) (PDMS) yielded a PDMS macroinitiator. This macroinitiator was used in atom transfer radical polymerization (ATRP) of styrene and isobornyl acrylate to produce ABA triblock copolymers. As a model for graft copolymers from a polyphosphazene backbone, chemical trans-­formation of hexachlorocyclotriphosphazene­resulted in hexafunctional molecules containing either benzyl bromide or bromopropionyl moieties. The initiator 1,1,3,3,5,5-hexakis[4-(2-bromopropionyloxymethyl)phenoxy]cyclotriphosphazene was used in the ATRP of styrene to yield a polymer with a narrow, monomodal molecular weight distribution. Chain extension of this star polymer with isobornyl acrylate is also described. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 1 Ill.
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  • 140
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 695-705 
    ISSN: 0268-2605
    Schlagwort(e): poly(silylenemethylene) ; polycarbo-­silane ; silicon carbide ; precursor ; polysilaethy-­lene ; disilacyclobutane ; pyrolysis ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Work carried in the authors laboratory on Si-CH2-Si bridged polycarbosilanes is reviewed. In pursuit of high-yield polymeric precursors to silicon carbide, convenient synthetic routes to both linear and hyperbranched polycarbosilanes having a ‘[SiH2CH2]n’ compositional formula have been developed. The linear [SiH2CH2]n polymer was prepared by ring-opening polymerization of a substituted disilacyclobutane, and was studied both as an analogue of polyethylene and as a high-yield precursor to SiC. Elaboration of the methods employed to prepare this polymer has yielded a wide range of new poly(silylenemethylene)s (PSMs) of the type [SiRR′CH2]n, where R and R′ can be a wide range of different groups, including a series of symmetrically disubstituted polymers with R = R′ = F, alkyl and alkoxy which form crystalline solid phases and various amorphous, atactic polymers having different R and R′ groups. By using (Si)-Cl replacement reactions analogous to those developed previously for polydichlorophosphazene, as well as hydrosilation reactions similar to those used for [Si(H)(Me)O]n, a series of side-chain polymers having various groups attached to Si through Si-C or Si-O bonded linkages were obtained. Similar polymer modification reactions have recently been developed for the branched oligomer/polymer analogue of these linear polycarbosilanes, leading to hyperbranched species with functional substituents, including a di(ethyleneoxy) methyl ether-terminated derivative which readily dissolves lithium salts. The results of studies of these novel ‘inorganic/organic’ hybrid polycarbosilanes are described and their properties are compared with those of related carbon-backbone and siloxane polymers. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 1 Tab.
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  • 141
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 787-792 
    ISSN: 0268-2605
    Schlagwort(e): tetrakis(dimethylamino)titanium ; amminolysis ; precursor ; pyrolysis ; titanium nitride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Precursors possessing Ti-N bonds were prepared by the reactions between Ti(NMe2)4 and each of three diamines H2NCH2CH2NH2, Me(H)NCH2CH2N(H)Me, HN(CH2CH2)2NH (Ti(NMe2)4:diamine = 1:2), and were converted into ceramics by pyrolysis. The reactions with H2NCH2CH2NH2 and HN(CH2CH2)2NH led to the formation of insoluble solids, whereas a soluble oil was obtained by the reaction with Me(H)NCH2CH2N(H)Me. The pyrolyses under argon gave carbon-rich Ti(N,C,O) phases,­but those under NH3- N2 resulted in the formation of Ti(N,C,O) phases with higher nitrogen contents. Despite the difference in precursor structures the pyrolysis behavior of three precursors under argon was rather similar, suggesting that the precursor obtained from Me(H)NCH2CH2N(H)Me was effectively cross-linked during pyrolysis. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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