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  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 49 (1993), S. 571-573 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 327 (1964), S. 147-150 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N-Brom-bis(trifluormethyl)-amin, (CF3)2NBr, reagiert mit NO2, NO und CO unter Bildung von (CF3)2NONO, (CO3)2NNO bzw. (CF3)2NCOBr. Das schon beobachtete einheitliche Reaktionsverhalten des (CF3)2NBr gegenüber einfachen ungesättigten Kohlenstoffverbindungen wurde auch bei C2H4, C2H2 sowie C2F4 gefunden, die (CF3)2NC2H4Br. (CF3)2NC2H2Br bzw. (CF3)2NC2F4Br ergeben. Mit AgCN wird CF3N = CF2 gebildet, und die Reaktion mit Ag2CO3 liefert als Hauptprodukt CF3N = NCF3.
    Notes: N-Bromobistrifluoromethylamine, (CF3)2NBr reacts with NO2, NO and CO to yield (CF3)2NONO, (CF3)2NNO and (CF3)2NCOBr, respectively. The reaction of (CF3)2NBr with unsaturated hydrocarbons and fluorocarbons has been confirmed, reaction with C2H4 C2H2 and C2F4 giving (CF3)2NC2H4Br, (CF3)2NC2H2Br and (CF3)2NC2F4Br. Reaction with AgCN yields CF3N = CF2, and that with Ag2CO3, CF3N = NCF3, as the chief product.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 79 (1967), S. 900-900 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 87 (1975), S. 208-209 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 14 (1975), S. 166-167 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1925-1931 
    ISSN: 0044-2313
    Keywords: Phosphorus compounds ; 3-Iod-5-alkyl-2,6,7-trichalcogena-1,3,4,5-tetraphospha-bicyclo[2.2.1.] heptan ; 3-Iod-6-alkyl-2,5,7-trichalcogena-1,3,4,6-tetra-phospha-bicyclo-[2.2.1.] heptan ; 3-Alkyl (Iod)-3,5,7-trithia-1,2,4,6-tetraphosphatricyclo[2.2.1.02,6] heptan ; 31P-NMR ; 77Se-NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Tetraphosphorus Trichalcogenides with Alkyl IodidesReactions of alkyl iodides RI (R = CHI2, CH2I or tert-Butyl) with P4E3 (E = S or Se) under the influence of light resulted in cleavage of the basal P3 ring. β-P4E3(I)R was formed initially, then it rearranged to the more stable α-P4E3(I)R structure. 31P NMR data of these products were measured and discussed, along with 77Se data for α- and β-P477SeSe2(I)CHI2. On reaction of P4S3 with tert-butyl iodide in CS2 or with sec-butyl iodide or iso-propyl iodide in dioxane, the new type of compounds P5S2R was observed. In this a sulfur bridge of P4S3 is replaced by a P—R group. 31P-NMR data for these compounds are reported.
    Notes: Bei der Reaktion von Alkyliodiden RI (R = CHI2, CH2I und tert-Butyl) mit P4E3 (E = S; Se) in CS2 wird unter Lichteinwirkung eine Bindung des basalen P3-Ring gebrochen. Es bildet sich β-P4E3(I)R, das sich nach einiger Zeit in das stabilere α-P4E3(I)R umwandelt. Die 31P-NMR Daten dieser Verbindungen und zusätzlich die 77Se-Daten für α- und β-P477SeSe2(I)CHI2 wurden gemessen und diskutiert. Bei der Reaktion von P4S3 mit tert-Butyliodid in CS2 bzw. mit sec-Butyliodid oder iso-Propyliodid in Dioxan wird der neue Verbindungstyp P5S2R beobachtet, in dem eine Schwefelbrücke des P4S3 durch eine P—R-Gruppe ersetzt ist, auch seine 31P-NMR-Daten werden wiedergegeben.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1115-1124 
    ISSN: 0044-2313
    Keywords: Bicyclic iodo tetrachalcogenatriphosphaheptanes ; Iodo dithiadiselenatriphosphabicyclo[2.2.1]heptane ; Iodo thiatriselenatriphosphabicyclo[2.2.1]heptane ; Iodo tetraselenatriphosphabicyclo[2.2.1]heptane ; Thiatetraselenadiphosphabicyclo[2.2.1]heptane ; 31P- 77Se-nmr ; intramolecular exchange ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bicyclic Iodo-tetrachalcogena-triphospha-heptanesThe compounds P3Se4-nSnI (n = 0, 1, 2) have been identified by 31P nmr spectroscopy. They were prepared by a direct thermal reaction of red phosphorus, sulfur, selenium and iodine in the stoichiometric ratio. These iodides could be converted into corresponding bromides and chlorides by substitution reactions. All molecules show a diselenium bridge in which, in contrast to the other selenium positions, selenium could not be replaced by sulfur. Similar effects were observed for the diselenium bridges of P2Se5. Systematic changes of the chemical shifts and coupling constants are caused by alterations in the molecular geometry, either by replacement of selenium by sulfur, or of iodine by more electronegative ligands. An intramolecular exchange reaction is observed for all molecules.
    Notes: Die Verbindungen P3Se4-nSnI (n = 0, 1, 2) wurden durch 31P-NMR-Spektroskopie als Reaktionsprodukte bei der thermischen Reaktion von rotem Phosphor, Schwefel, Selen und Iod im entsprechenden Verhältnis beobachtet. Über Substitutionsreaktionen konnten diese Iodide in die Bromide und Chloride überführt werden. Alle Moleküle besitzen eine Diselenbrücke, in der das Selen, im Gegensatz zu den anderen Selenpositionen, nicht durch Schwefel ersetzt werden kann. Die gleiche Beobachtung wird auch an den beiden Diselenbrücken des P2Se5 gemacht. Systematische Veränderungen der chemischen Verschiebungen und der Kopplungskonstanten werden durch Verzerrung des Molekülgerüstes beim Ersatz von Selen durch Schwefel oder des Iods durch elektronegativere Liganden hervorgerufen. In allen Molekülen ist ein intramolekularer Austauschprozeß zu beobachten.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-2313
    Keywords: 31P NMR spectroscopy ; phosphorus compounds ; 3-Iod-5-methoxy-2,6,7-trithia-1,3,4,5-tetraphospha-bicyclo-[2.2.1.]heptan ; 3,5-dimethoxy-2,6,7-trithia-1,3,4,5-tetraphosphabicyclo[2.2.1.]heptan ; 3-Iod-6-alkoxy-2,5,7 trichalkogena-1,3,4,6-tetraphospha-bicyclo[2.2.1.]heptan ; 3,6-dialkoxy(alkylthio)-2,5,7-chalkogena-1,3,4,6-tetraphospha-bicyclo[2.2.1.]-heptan ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Alcohols and Mercaptans with Tetraphosphorus Trichalcogenide Diiodidesα-P4E3(I)R and α-P4E3R2 (R = -OCH3, -OC2H5, -OCH(CH3)2, -OC(CH3)3 and -OC6H5) have been detected in the reaction solutions of α-P4E3I2 (E = S, Se) with alcohols in the presence of triethylamine, or with trimethyltin alkoxides in CS2. β-P4S3I2 reacted with methanol at 243 K in CS2 to yield β-P4S3(I)OCH3, β-P4S3(OCH3)exo(OCH3)endo, and β-P4S3[(OCH3)exo]2. The thiolates α-P4Se3R2′ (R′ = -SC2H5, -n-SC5H11, -n-SC7H15, -SC(CH3)3 and -SC6H5) were found in reaction solutions of α-P4Se3I2 with thiols HR′. The 31P NMR data of these compounds are given.
    Notes: Durch die Umsetzung von α-P4E3I2 (E = S, Se) mit Alkoholen in Gegenwart von Triethylamin oder mit Trimethylzinnalkoxyverbindungen in CS2 wurden α-P4E3(I)R und α-P4E3R2 (R = -OCH3, -OC2H5, -OCH(CH3)2, -OC(CH3)3 und -OC6H5) in den Reaktionslösungen nachgewiesen. β-P4S3I2 wurde bei 243 K in CS2 mit Methanol zur Reaktion gebracht und ergab β-P4S3(I)OCH3, β-P4S3(OCH3)exo(OCH3)endo und β-P4S3[(OCH3)exo]2. In Reaktionslösungen von Thiolen, HR′ (R′ = -SC2H5, -n-SC5H11, -n-SC7H15, -SC(CH3)3 und -SC6H5), mit α-P4Se3I2 wurden die Thiolate, α-P4Se3R2′, identifiziert. Die 31P-NMR-Daten dieser Verbindungen werden angegeben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 6 (1967), S. 878-878 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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