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  • 1
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Spyrohydantoines Derivatives of 2,4-Diphenyl-3-azabicyclo[3.3.1]nonane and 7,9-Diphenyl-8-azabicyclo[4.3.1]decane via Bucherer Reaction in N,N-Dimethylformamide: Influence of the Temperature and Stereochemical PathThe unreactives ketones related to 2,4-diphenyl-3-azabicyclo [3.3.1]nonan-9-one to the Bucherer reaction in usuals conditions show excellent reactivity in DMF. as unique solvant. The stereochemical paths of these reactions and the synthetic utility of the temperature modification are described.
    Additional Material: 1 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 3518-3520 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unusual Reactivity of Strained Bridgehead DerivativesThe solvolysis of 7,7-dimethyl-1, exo-2-bis(trifluoromethylsulfonyloxy)norbornane (5) in Et2O/I2Mg and 80% MeOH proceeds with formation of substituted 2-norbornyl cations, yielding 1, exo-2-diiodo-7,7-dimethylnorbornane (9) and camphenilone (13), respectively. When the vic-diiodide 9 is treated with LiAlH4/C6H6 partial epimerization to 1,endo-2-diiodo-7,7-dimethylnorbornane (12) is observed without reduction; this result is probably due to steric hindrance of the reactants.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 815-818 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Steric Control in the Reaction of Substituted 2-Norbornyl CationsThe reaction of camphenilone (1b) with trifluoromethanesulfonic anhydride (Tf2O) yields 7,7-dimethyl-1,exo-2-bis(trifluoromethylsulfonyloxy)norbornane (4b) (60%). 6,6-Dimethyl-2-norbornanone (1c) affords under the same conditions 6,6-dimethyl-2-norbornen-2-yl triflate (5c) (70%). The reaction pathways of the intermediate 2-(trifluoromethylsulfonyloxy)-2-norbornyl cations are mostly controlled by steric factors, the inductive effect playing no significant role.
    Additional Material: 1 Tab.
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A spectroscopic (UV, IR, 1H NMR) study of the cationic polymerisation of 2-vinylfuran (1a) and 2-isopropenylfuran (2a) showed the existence of an important alkylation reaction at C5 which competes with normal propagation. The extent of this competition depends on the monomer used and the polymerisation temperature. A comparison of the spectra of standard polymers (prepared by radical or stereospecific polymerisation) with those of polymers obtained by cationic initiation allowed to assess the extent of alkylation and its regiospecificity at C5 2-Methyl-5-vinylfuran (1b) and 2-methyl-5-isopropenylfuran (2b) were found to undergo cationic polymerisation without any interference from alkylation reactions. Reactions between these four monomers and 2-methylfuran in the presence of typical acidic catalysts gave very high yields of alkylated products and no polymerisation, thus confirming the importance of this electrophilic reaction and its possible application to synthetic uses.
    Additional Material: 15 Ill.
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anionic polymerization of p-triphenylgermylstyrene (1a) and p-tributylgermylstyrene (1b) were investigated under high vacuum conditions (≈10-6 mbar). Both 1a and 1b were readily polymerized with sodium naphthalide, potassium naphthalide, or α-methylstyrylsodium oligomers to form “living polymers”. The addition of α-methylstyrene to these living systems gave the triblock copolymer, poly(α-methylstyrene-b-p-triphenylgermylstyrene-b-α-methylstyrene). Both monomers were also polymerized radically with AIBN as initiator. Some physical properties of the resulting polymers were examined.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 23 (1983), S. 766-770 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Water-ground Phlogopite mica (Kemira Siilinjarvi phlogopite) has been evaluated as a reinforcing filler in polypropylene. The major factors which influence the composite strength and modulus include the size, aspect ratio, and uniformity of the mica flakes. Aqueous delamination permits the production of very small flakes (less than 44 microns diameter) with aspect ratios near 50. Such small flakes impart greater tensile and modulus values to polypropylene than larger flakes and the former can also be reprocessed many times without any deterioration of properties. Surface treatment is necessary for adequate dispersion and coupling, particularly with the finely divided mica fillers. Other properties such as the heat-distortion temperature, fracture toughness, and gas permeability are also influenced by the mean size and aspect ratio of the mica filler. Guidelines are presented to indicate the preferred characteristics of mica fillers for optimum performance.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 33-43 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Four poly(vinyl chloride) (PVC) samples, 1, 2, 3, and 4, were prepared in bulk using 2,2′-azodiisobutyronitrile at 90°C and 60°C and the same initiator together with UV irradiation at 0°C and -50°C, respectively. Fractions were obtained from samples 2,3, and 4 by extracting with acetone, sample 1 being completely soluble in this solvent. The whole PVC's as well as their acetone soluble and insoluble fractions, were characterized by determining the intrinsic viscosity, the osmometric molecular weight, and the tacticity; then they were thermally degraded up to conversion of 0.3% in powder state. The values of degradation rate for both the insoluble fractions and the whole PVC's were in agreement with some prior results on the influence of syndiotactic sequences on propagation step. The soluble fractions proved to be very unstable in comparison with the insoluble, which, despite the lower molecular weight of the former, seems to obey their higher content of isotactic conformations. The fine polyene distribution in the degraded polymers was carried out by UV-visible spectroscopy. The results reveal the occurrence of two different polyene distributions, and allow for the peculiar one of the soluble fractions to be related to polyenes consisting of two sequences of trans conjugated double bonds separated by a single cis double bond. The results clearly shows that there are two mechanisms for initiation of the PVC degradation, depending on whether it occurs by random unstable structures or by the normal GTTG isotactic or TTTG heterotactic triads. Moreover, these two initiation processes are proved to give rise to different types of polyenes, which accounts for the occurrence of two unlike mechanisms of propagation.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 1127-1132 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction SO + SO →l S + SO2(2) was studied in the gas phase by using methyl thiirane as a titrant for sulfur atoms. By monitoring the C3H6 produced in the reaction \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm S} + {\rm CH}_3\hbox{---} \overline {{\rm CH\hbox{---}CH}_2\hbox{---} {\rm S}} \to {\rm S}_2 + {\rm C}_3 {\rm H}_6 (7) $\end{document}, we determined that k2 ≃ 3.5 × 10-15 cm3/s at 298 K.
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  • 9
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 4 (1983), S. 297-301 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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