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  • Anthraflavates  (1)
  • TAAB  (1)
  • X-ray diffraction analysis  (1)
  • 1
    ISSN: 1572-8854
    Schlagwort(e): Anthraflavates ; tetraaza ; TAAB
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract Charge transfer molecular solids [diaqua tetrabenzo (b,f,j,n,) {1,5,9,13) tetraazacyclohexadecine] Ni(II) and Cu(II) bisanthraflavates were synthesized and characterized by IR, Mass Spectrometry, TGA, and X-ray diffraction on single crystals. Unit cell dimensions (Å) a = 12.291(1), c = 14.574(1) Å and a = 12.434(1), c = 14.066(1) Å for Cu(II) and Ni(II) derivatives, respectively, space group P42/n in both cases. The obtained compounds show expected chemical and structural similarities. Tetraazamacrocycles are surrounded individually by a zig-zag, ribbon-like motif extending in the crystal by head-to-tail hydrogen bonding of monosubstituted anthraflavates. Electric conductivities were measured by the four points method as pellets from the variation of electric current through the sample as a function of temperature, for fixed voltages in the ohmic regime. Preliminary results indicate low conductivity values at room temperature but semiconductivity behaviour in the temperature range −150 to 170°C.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1573-9171
    Schlagwort(e): photolysis ; ferrocenylcyclopropene ; tricyclohexane ; vinylcarbenes ; cyclobutene ; X-ray diffraction analysis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Photolysis of 3-ferrocenyl-3-methyl- and 3-ferrocenyl-3-isopropylcyclopropenes was studied. Sensitized irradiation (triplet excitation) afforded [2+2]-cycloaddition products, viz., tricyclohexane derivatives. Direct irradiation (singlet excitation) of methyl-substituted ferrocenylcyclopropene gave rise to 2-ferrocenylbut-1-en-3-yne and trans-2-ferrocenylbut-2-ene. The isopropyl analog was converted into 1-ferrocenyl-4,4-dimethylcyclobutene. The reaction of this cyclopropene with 2-ferrocenyl-3-methylbut-1-ene afforded 1,3-diferrocenyl-3-isopropyl-6,6-dimethylcyclohexene. The latter compound and 3,6-diferrocenyl-3,6-diisopropyltricyclo[3.1.0.02,4]hexane were studied by X-ray diffraction analysis. Possible reaction pathways are discussed.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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