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  • 1
    ISSN: 1434-1948
    Keywords: Arsonium salts ; Superacidic systems ; Structure elicidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of trimethylarsane in the superacidic systems hydrogen/fluoride antimony pentafluoride and hydrogen fluoride/arsenic pentafluoride leads to trimethylarsonium fluorometallates. These salts are stable up to 60 °C and 5 °C, respectively. Structures were successfully elucidated in the cases of trimethylarsonium undecafluorodiarsenate and trimethylarsonium hexafluoroantimonate. (CH3)3AsH+As2F11- crystallizes in the monoclinic space group P21/n with four formula units per unit cell with the dimensions a = 7.362(1), b = 12.589(1), c = 13.598(1) Å and β = 95.37(1)°. (CH3)3AsH+SbF6- crystallizes in the monoclinic space group P21/m with four formula units per unit cell with the dimensions a = 8.313(1), b = 8.855(1), c = 13.285(1) Å and β = 94.358(1)°.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1377-1380 
    ISSN: 1434-1948
    Keywords: Ab initio calculations ; Electronic structure ; Photoelectron spectroscopy ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electronic structure of the title compound 1 has been investigated by UV photoelectron spectroscopy and quantum chemical calculations. 1 has two nearly degenerate nN lone-pair orbitals which form the two highest occupied MOs. The third highest occupied MO is mainly localized at the oxygen atom (n0). All calculations indicate that the molecule has a twisted C2 conformation.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: Chlorine trifluoromethyloxonium-, chlorine methyloxonium hexafluoroantimonate and -arsenate ; vibrational, nmr, mass spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Reactions of CH3OCl, CF3OCl, CF3OF, and CF3OH with the Superacid System HF/MF5 (M = As, Sb). Preparation and Characterization of CH3OCl(H)+MF6- and CF3OCl(H)+MF6-The preparation of the chlorine oxoniumsalts CH3OCl(H)+MF6- and CF3OCl(H)+MF6- by protonation of CH3OCl and CF3OCl in the superacid solution of HF/MF5 (M = As, Sb) is described. However CF3OF and CF3OH have not been protonated under the same conditions. In the case of CF3OH the formation of F2CO · MF5 is observed. The novel compounds are characterized by nmr- and vibrational spectroscopy.
    Notes: Es wird über die Darstellung der Chloroxoniumsalze CH3OCl(H)+MF6- und CF3OCl(H)+MF6- durch Protonierung von CH3OCl und CF3OCl in dem supersauren System HF/MF5 (M = As, Sb) berichtet. Dagegen lassen sich CF3OF und CF3OH bei gleichen Bedingungen nicht protonieren. CF3OH bildet in supersaurer Lösung die Addukte F2CO · MF5. Die Charakterisierung aller neuen Verbindungen erfolgt NMR- und schwingungsspektroskopisch.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0044-2313
    Keywords: Chlorine Nitrate ; Tetramethylammoniumtrifluoromethylnitratoiodate(I) ; (CH3)4N+CF3IONO2- ; vibrational spectra ; Halogen Nitrates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation and Spectroscopic Characterization of Tetramethylammoniumtrifluoromethylnitratoiodate(I) (CH3)4N+CF3IONO2-(CH3)4N+CF3ICI- reacts with CIONO2 to (CH3)4N +CF3IONO2-. The salt is characterized by vibrational spectra.
    Notes: (CH3)4N+CF3ICI- reagiert mit ClONO2 unter Chlorkomproportionierung zu (CH3)4N+CF3IONO2-. Das erhaltene Salz wird schwingungsspektroskopisch charakterisiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0044-2313
    Keywords: Tetramethylammoniurn bistrifluoromethylnitrate ; tetramethylammonium trifluoromethylbistrifluoromethylnitroxyliodate(I) ; bistrifluorometylnitroxyde ; vibrational spectra ; 19F, 13C NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Preparation of Tetramethylammonium Trifluoromethylbistritluoromethylnitroxyliodate(I) (CH3)4N+(CF3)2NOICF3- and the Reaction of Tetramethylammonium Bistrifluoromethylnitrate (CH3)4N+(CF3)2NO- with Cl2 and ClONO2The preparation of (CF3)2NO- as tetramethylammoniumsalt and its addition reaction with CF3I are described. The formed Tetramethylammonium trifluoromethylbistrifluoromethylnitroxyliodate(I) (CH3)4N+(CF3)2NOICF3 is characterized by its spectra and the reaction with CF3OCl.In addition we present our approach to the preparation of (CF3)2NOCl by the reaction of (CH3)4N+(CF3)2NO- with Cl2 and ClONO2The thermolabile compounds have been characterized by i.r., Raman, 19F and 13C NMR spectra.
    Notes: Es wird über die Darstellung von (CF3)2NO- als Tetramethylammoniumsalz und seiner Additionsreaktion mit CF3I berichtet. Das auf diesem Wege dargestellte Tetramethylammonium-Trifluormethylbistrifluormethylnitroxyliodat(I) (CH3)4N+(CF3)2NOICF3- wird spektroskopisch und durch die Reaktion mit CF3OCI charaklerisiert.Weiterhin werden Versuche zur Darstellung von (CF3)2NOC1 durch die Reaktion von (CH3)4N+(CF3)2NO mit Cl2 und ClONO2 vorgestellt.Die zum Teil thermolabilen Verbindungen werden durch IR-, Raman- sowie Multikern-NMR-Spektroskopie charakterisiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0044-2313
    Keywords: N,N-Dichloromethylsulfonammonium salts ; crystal structure of CH3S(O)2NCl2 ; vibrational spectra ; 1H ; 13C ; 19F NMR ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New N,N-Dichloromethylsulfonammonium Salts CH3S(O)2NCl2X+MF6- (X = CH3, Cl, F; M = As, Sb) and Crystal Structure of CH3S(O)2NCl2The preparations of new dichlorammonium salts CH3S(O)2NCl2X+MF6- (X = CH3, Cl, F; M = As, Sb) and of CH3S(O)2NCl2 by oxidative halogenation respectively methylation are reported. The thermolabil compounds are characterized by IR, Raman, 1H, 13C, 19F NMR spectroscopy. N,N-Dichlormethylsulfonamid CH3S(O)2NCl2 crystallizes at 173(1) K in the orthorhombic space group Pnma with a = 615.1(3) pm, b = 937.3(5) pm, c = 970.3(5) pm and Z = 4.
    Notes: Die Darstellung einer Reihe von Dichlor ammoniumsalzen des Typs CH3S(O)2NCl2X+MF6- (X = CH3, Cl, F; M = As, Sb) wird angegeben. Die Salze werden durch oxidative Halogenierung bzw. Methylierung von CH3S(O)2NCl2 erhalten. Die Charakterisierung der thermolabilen Verbindungen erfolgte mittels IR-, Raman-sowie Multikern-NMR-Spektroskopie. Die Einkristallröntgenstrukturanalyse von N,N-Dichlormethylsulfonamid CH3S(O)2NCl2 bei 173(1) K ergab: orthorhombische Raum gruppe Pnma mit a = 615,1(3) pm, b = 937,3(5) pm, c = 970,3(5) pm und Z = 4.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 653-656 
    ISSN: 0009-2940
    Keywords: Hydroxylamine, O-methyl-N,N-bis(trifluoromethyl)-, gas-phase structure of ; Electron diffraction ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular structure of (CF3)2NOCH3 was determined by gas electron diffraction. The molecular intensities were reproduced by use of a single conformation with syn orientation of the O-CH3 group relative to the nitrogen lone pair. This was confirmed by ab initio calculations (HF/3-21G(*), polarization functions only on nitrogen, and MP2/6-31G*). The observed structure demonstrates that the generalized anomeric effect is of minor importance to this compound. The following skeletal geometric parameters (bond lengths [pm] and angles [°] with 3-s̰ uncertainties) were derived: N-C 142.9(7), N-O 142(3), O-C 145(3), CNC 118.0(9), CNO 108.1(17), and NOC 109.4(17). The experimental structure is well reproduced by the ab initio calculations.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 107 (1995), S. 1653-1653 
    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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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 109 (1997), S. 1579-1580 
    ISSN: 0044-8249
    Keywords: Fluor ; Elektronenbeugung ; Stickstoff ; Strukturaufklärung ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 487-490 
    ISSN: 0044-2313
    Keywords: Tetramethylammonium bistrifluormethoxybromate(I) ; vibrational spectra ; 19F ; 13C NMR ; mass spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of Tetramethylammonium Bistrifluormethoxybromate(I) (CH3)4N+Br(CF3O)2-We describe the preparation and characterization of (CH3)4N+Br(CF3O)2-. It is prepared via comproportionation of CF3OCl with (CH3)4N+BrCl2- under formation of Cl2 at -70°C, respectively via addition elimination reaction of CF3OCl with (CH3)4N+Br- at -70°C. The thermolabile salt is characterized by i.r., Raman, 19F, 13C NMR and mass spectroscopy.
    Notes: Es wird über die Darstellung und Charakterisierung von (CH3)4N+Br(CF3O)2- berichtet. (CH3)4N+Br(CF3O)2- erhält man sowohl durch Komproportionierung von CF3OCl mit (CH3)4N+BrCl2- bei -70°C unter Bildung von elementarem Chlor, als auch über die Additions-Eliminierungsreaktion von CF3OCI mit (CH3)4N+Br bei-70°C. Die thermolabile Verbindung wird durch IR-, Raman-, 19F-, 13C-NMR sowie Massenspektroskopie charakterisiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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