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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1309-1313 
    ISSN: 1434-1948
    Keywords: Phthalocyanines ; Rhenium ; Nitrido(octa-n-alkylphthalocyaninato)rhenium compounds ; Nucleophilic additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of nitrido(tetra-tert-butylphthalocyaninato)rhenium (1) with boron tribromide leading to (tBu4Pc)ReNBBr3 (4) and with acetone to give the imido complex (tBu4Pc)Re[NC(CH3)2CH2C(O)CH3]OH (2b) and its μ-oxo dimer 3 are reported. Starting from the corresponding 4,5-di-n-alkylphthalonitriles and ammonium perrhenate four soluble nitrido(octa-n-alkylphthalocyaninato)rhenium complexes 5-8 were synthesized. Nitrido(octa-n-pentylphthalocyaninato)rhenium (6) was treated with boron tribromide to afford [(C5H11)8Pc]ReNBBr3 (9).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 91 (1958), S. 1552-1555 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das aus 1-Methyl-cyclopentanon-(2) über die 3-Hydroxymethylen-Verbindung erhaltene 1-Methyl-3-[N-methyl-anilinomethylen]-cyclopentanon-(2) und Bromessigester kondensieren sich mittels NaNH2 zum Ester II, der als Rohprodukt bei alkalischer Verseifung unter gleichzeitiger Abspaltung des N-Methyl-anilinomethylen-Restes 1-Methyl-cyclopentanon-(2)-essigsäure-(1) liefert, die mit Diazomethan den Methylester gibt. Analog wird aus dem bereits bekannten 1-Methyl-3-[N-methyl-anilinomethylen]-cyclohexanon-(2) der 1-Methyl-cyclohexanon-(2)-essigsäure-(1)-äthylester gewonnen.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclopentanon-(2)-essigsäure-(1)-äthylester und Cyclohexanon-(2)-essigsäure-(1)-äthylester werden mit Phenyl-magnesiumbromid zu γ-Lactonen umgesetzt, aud denen nach Clemmensen-Martin-Reduktion und Cyclisierung mit wasserfreier Flußsäure 1-Keto-tetrahydro-3,4-cyclopenteno-naphthalin bzw. cis- und trans-9-Keto-octahydro-phenanthren entstehen. Mit β-Naphthyl-magnesiumbromid als Grignard-Komponente kommt man in die Reihe des Tetrahydro-1,2-cyclopenteno-phenanthrens und der Octahydro-chrysene; wird dabei an Stelle von Cyclopentanon-(2)-essigsäure-(1)-äthylester der 1-Methyl-cyclopentanon-(3)-essigsäure-(2)-äthylester verwendet, so gelangt man über analoge Zwischenstufen zum Diels'schen Kohlenwasserstoff.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1681-1685 
    ISSN: 0009-2940
    Keywords: Rhenium(V), nitrido(tetra-tert-butylphthalocyaninato)- ; Rhenium(V), nitrido(phthalocyaninato)- ; Phthalocyaninato complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4-tert-Butylphthalodinitrile (1) reacts with ammonium perrhenate, NH4ReO4, to yield nitrido(tetra-tert-butylphthalocyaninato)rhenium(V), (tBu)4PcReN (2), which is characterized by IR, UV/Vis, CV, MS, 1H and 13C NMR, and elemental analysis. It shows good solubility in common organic solvents. In solution 2 is assumed to be monomeric whereas in the solid state also dimers or higher aggregates are present. From the NMR spectra it is concluded that different constitutional isomers of 2 are formed but not in the expected ratio of a statistical distribution. By analogy with 2, the already known nitrido(phthalocyaninato)rhenium(V), PcReN (3), is prepared for comparison.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2559-2563 
    ISSN: 0009-2940
    Keywords: μ-Cyano(2,3-naphthalocyaninato)iron(III) ; Potassium dicyano(2,3-naphthalocyaninato)ferrate(III) ; Dichloro(2,3-naphthalocyaninato)iron(III) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Potassium dicyano(2,3-naphthalocyaninato)ferrate(III), K[2,3-NcFe(CN)2] (2), reacts in water with elimination of KCN to form μ-cyano(2,3-naphthalocyaninato)iron(III), [2,3-NcFe(CN)]n (4a). Dichloro(2,3-naphthalocyaninato)iron(III), 2,3-NcFeCl2 (3), reacts with KCN to yield also [2,3-NcFe(CN)]n (4b). Both compounds 4a and 4b show similar IR spectra with a typical blue-shifted CN valence frequency caused by a bridging function of CN-. Compounds 4a and 4b also show almost identical 57Fe-Mössbauer spectra which, however, might be interpreted with a Fe(+II) oxidation state of the iron. The measured magnetic moment of 4 however clearly proves the expected oxidation state +III of the iron in [2,3-NcFe(CN)]n (4). Compounds 4a and 4b both exhibit good semiconducting properties (σRT ∼ 10-3 S/cm) without additional external oxidative doping. The property is quite similar to that of the known μ-cyano(phthalocyaninato)iron [PcFe(CN)]n (σRT ∼ 10-2 S/cm).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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