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  • 1
    Electronic Resource
    Electronic Resource
    Neue Alkylchlorsulfonium-Salze und Kristallstruktur von Diethylchlorsulfoni-umhexachloroantimonat (C2H5)2SCl+SbCl6- (1995)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1547-1551 
    Details
    ISSN: 0044-2313
    Keywords: Dialkylchlorosulfonium hexachloroantimonates ; crystal structure ; preparation ; IR, Raman, NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New Alkylchlorosulfonium Salts and Crystal Structure of Diethylchlorosulfonium-Hexachloroantimonate (C2H5)2SCl+SbCl6-We describe the preparation and spectroscopic characterization of Dialkylchlorosulfonium-Hexachloroantimonates R2SCl+SbCl6- (R = C2H5, i-C3H7) and the crystal structure of Diethylchlorosulfonium-Hexachloroantimonate (C2H5)2SCl+SbCl6- at 172(1) K. The salt crystallize in the orthorhombic space group P212121 with a = 980.4(13) pm, b = 1010.6(8) pm, c = 1492.8(14) pm with four formula units per unit cell.
    Notes: Es wird die Darstellung und spektroskopische Charakterisierung von Dialkylchlorsulfoniumhexachloroantimonaten R2SCl+SbCl6- (R = C2H5, i-C3H7), sowie die Einkristallröntgenstrukturanalyse von Diethylchlorsulfoniumhexachloroantimonat (C2H5)2SCl+SbCl6- bei 172(1) K beschrieben. Das Salz kristallisiert in der orthorhombischen Raumgruppe P212121 mit a = 980,4(13) pm, b = 1010,6(8) pm, c = 1492,8(14) pm mit 4 Formeleinheiten pro Elementarzelle.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19956210919
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  • 2
    Electronic Resource
    Electronic Resource
    Reaktion von Chlornitrat mit CF3I: Isolierung von Trifluormethylchloriodnitrat CF3I(Cl)ONO2 und Kristallstruktur von Trifluormethylioddinitrat CF3I(ONO2)2 (1995)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1552-1557 
    Details
    ISSN: 0044-2313
    Keywords: Chlorine Nitrate ; Trifluormethylchloroiodinenitrate ; Trifluormethyliodinedinitrate ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Chlorine Nitrate with CF3I: Isolation of Trifluormethylchloroiodinenitrate CF3I(Cl)ONO2 and the Crystal Structure of Trifluormethyliodinedinitrate CF3I(ONO2)2CF3I reacts with ClONO2 to Iodine(III)-compounds. After an addition CF3I(Cl)ONO2 is isolated and characterized by vibrational spectra. With surplus ClONO2 it is formed CF3I(ONO2)2.CF3I(ONO2)2 crystallizes monoclinic in the space group P21/c with the cell parameters a = 1 024.3(6) pm, b = 873.5(6) pm, c = 873.4(6) pm and Z = 4.We measered following bonding distances: I—O: 207.3(3) and 220.8(2) pm, I—C: 221.1(4) pm and N—O: from 119.1(4) to 141.5(3) pm.Through an intermolecular I ··· O-contact the central iodine becomes a distorted plane geometry.
    Notes: CF3I reagiert mit ClONO2 in einer oxidativen Additionsreaktion zu Iod(III)-Verbindungen. Das Additionsprodukt CF3I(Cl)ONO2 wird isoliert und schwingungsspektroskopisch charaktersiert. Mit überschüssigem ClONO2 bildet sich CF3I(ONO2)2.CF3I(ONO2)2 kristallisiert monoklin in der Raumgruppe P21/c mit a = 1 024,3(6) pm, b = 873,5(6) pm, c = 873,4(6) pm und Z = 4.Es werden folgende Bindungslängen gemessen: I—O: 207,3(3) bzw. 220,8(2) pm, I—C: 221,2(4) pm und N—O: 119,1(4) bis 141,5(3) pm.Durch einen intermolekularen I ··· O-Kontakt erlangt das zentrale Iodatom eine verzerrt-planare Umgebung.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19956210920
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  • 3
    Electronic Resource
    Electronic Resource
    Kristallstruktur einer neuen Modifikation von Sb8F30 (1991)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 605 (1991), S. 109-116 
    Details
    ISSN: 0044-2313
    Keywords: Antimony(III)fluoride,(Sb2F5+)(Sb3F72+)(SbF6-)3 ; preparation ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structure of a new Modification of Sb8F30The modification of Sb8F30, described here, crystallizes in the orthorhombic space group Pca21 (No. 29) with a = 1115.7(1), b = 1100.2(1), c = 1917.8(3) pm and Z = 4. Within this complex molecule, the Sb3F72+-cation was identified besides a heavily distorted form of the mixed valent Sb4F17--anion.
    Notes: Die hier beschriebene Modifikation von Sb8F30 kristallisiert in der orthorhombischen Raumgruppe Pca21 (Nr. 29) mit a = 1115,7(1), b = 1100,2(1), c = 1917,8(3) pm und Z = 4. Innerhalb dieses komplexen Moleküls werden ein Sb3F72+-Kation und eine stark verzerrte Form des gemischt valenten Sb4F17--Anions identifiziert.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19916050112
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  • 4
    Electronic Resource
    Electronic Resource
    Über die Kristallstrukturen von CH3PF2H+AsF6- und CH3PF2H+SbF6- und eine einfache Darstellung von CH3PF2 (1994)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 509-513 
    Details
    ISSN: 0044-2313
    Keywords: (difluoro)methylphosphine ; (difluoro)methylphosphonium salts ; preparation ; single crystall X-ray structure ; vibrational and NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Crystal Structures of CH3PF2H+AsF6- and CH3PF2H+SbF6- and a simple Method for Preparation of CH3PF2A simple method for preparation of CH3PF2 from CH3PCl2 is reported. The phosphonium salts CH3PF2H+MF6- are obtained by the reaction of CH3PCl2 with superacidic systems HF/MF5 (M = As, Sb). CH3PF2H+SbF6- crystallizes in the space group P1 with a = 548.4(4) pm, b = 695.5(8) pm, c = 960.2(9) pm, α = 94.68(5)°, β = 97.19(6)°, γ = 94.41(6)° and Z = 2. CH3PF2H+SbF6- crystallizes in P1 with a = 554.3(3), b = 724.2(4), c = 970.4(5), α = 94.73(4)°, β = 96.14(5)°, γ = 95.30(4)°.
    Notes: Es wird über eine einfache Darstellung von CH3PF2 aus CH3PCl2 berichtet, welches in den supersauren Systemen HF/MF5 (M = As, Sb) zu den Phosphoniumsalzen CH3PF2H+MF6- protoniert wird. CH3PF2H+AsF6- kristallisiert in der Raumgruppe P1 mit a = 548,4(4) pm, b = 695,5(8) pm, c = 960,2(9) pm, α = 94,68(5)°, β = 97,19(6)°, γ = 94,41(6)° und Z = 2, das isostrukturelle CH3PF2H+SbF6- mit a = 554,3(3), b = 724,2(4), c = 970,4(5), α = 94,73(4)°, β = 96,14(5)°, γ = 95,30(4)°.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19946200319
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  • 5
    Electronic Resource
    Electronic Resource
    Fluorieren mit Trifluormethylhypochlorit CF3OCl. Darstellung und Kristallstrukturanalyse von Trifluormethyliodtetrafluorid CF3IF4Professor Peter Paetzold zum 60. Geburtstag gewidmet (1995)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1247-1250 
    Details
    ISSN: 0044-2313
    Keywords: Trifluoromethyliodine tetrafluoride ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Fluorinate with Trifluoromethylhypochlorite CF3OCl. Preparation and Crystal Structure Determination of Trifluoromethyliodine Tetrafluoride CF3IF4The preparation of Trifluoromethyliodine tetrafluoride (CF3IF4), from Trifluoromethyliodide (CF3I) with Trifluoromethylhypochlorite (CF3OCl), and the crystal structure of CF3IF4 at 172(1) K is described. CF3IF4 crystallizes in the monoclinic space group P21/c with a = 762.2(7) pm, b = 842.9(10) pm, c = 856.4(7) pm, β = 99.65(7)° with four formula units per unit cell.
    Notes: Es wird die Darstellung von Trifluormethyliodtetrafluorid (CF3IF4), aus Trifluormethyliodid (CF3I) und Trifluormethylhypochlorit (CF3OCl), sowie die Kristallstrukturanalyse bei 172(1) K beschrieben. CF3IF4 kristallsiert in der monoklinen Raumgruppe P21/c mit a = 762,2(7) pm, b = 842,9(10) pm, c = 856,4(7) pm, β = 99,65(7), Z = 4.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19956210724
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