ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • bis(phosphane) sulphur dioxide nickel(0) complexes  (1)
  • guanidinium tetrafluorodioxowolframate  (1)
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 604 (1991), S. 77-83 
    ISSN: 0044-2313
    Keywords: Guanidinium hexafluorometallates ; guanidinium pentafluorooxoniobate ; guanidinium tetrafluorodioxowolframate ; preparation ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Guanidinium Hexafluorometallates of Titanium, Silicon, Germanium, and Tin. Guanidinium Pentafluorooxoniobate and Guanidinium TetrafluorodioxowolframateThe title compounds were crystallized from the aqueous solutions of their fluorometallate respectively oxofluorometallate acids by adding of guanidinium fluoride solution. Their unit cells were determined and for [C(NH2)3]2 TiF6 its crystal structure was determined: s. g. Cm, a = 12.869 Å, b = 7.378 Å, c = 6.243 Å, β = 114.45°, layer structure, R = 0.0257. The unit cell parameters of [C(NH2)3]2 SiF6: a = 12.612 Å, b = 7.272 Å, c = 6.171 Å, β = 114.30°, of [C(NH2)3]2 GeF6: a = 12.773 Å, b = 7.343 Å, c = 6.202 Å, β = 114.38°, of [C(NH2)3]2 SnF6 : a = 12.972 Å, b = 7.439 Å, c = 6.356 Å, β = 114.14°, of [C(NH2)3]2 NbOF5:a = 12.987 Å, b = 7.425 Å, c = 6.326 Å, β = 114,25°, of [C(NH2)3]2 WO2F4:a = 12.941 Å, b = 7.396 Å, c = 6.256 Å, β = 114.33°.
    Notes: Die Titelverbindungen wurden aus den wässrigen Lösungen der jeweiligen Fluorometallat-bzw. oxofluorometallatsäuren nach Zugabe von Guanidiniumfluoridlösung als kristalline Verbindungen erhalten und ihre Gitterkonstanten bestimmt. Vom [C(NH2)3]2 Tif6 wurde die Kristallstruktur bestimmt: R.Gr. Cm, a = 12,869 Å, b = 7,378 Å, c = 6,243 Å, β = 114,45°, Schichtstruktur, R = 0,0257. Kristallographische Daten von [C(NH2)3]2 SiF6:a = 12,612 Å, b = 7,272 Å, c = 6,171 Å, β = 114,30°, von [C(NH2)3]2 GeF6:a = 12,773 Å, b = 7,343 Å, c = 6,202 Å, β = 114,38°, von [C(NH2)3]2 SnF6:a = 12,972 Å, b = 7,439 Å, c = 6,356 Å, β = 114,14°, von [C(NH2)3]2 NbOF5:a = 12,987 Å, b = 7,425 Å, c = 6,326 Å, β = 114,25°, von [C(NH2)3]2 WO2F4:a = 12,941 Å, b = 7,396 Å, c = 6,256 Å, β = 114,33°.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0044-2313
    Keywords: I. r. and 31P n. m. r. spectroscopy ; bis(phosphane) sulphur dioxide nickel(0) complexes ; X-ray structure of Ni(PCy3)2(SO2) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Sulphur Dioxide as Ligand and Synthon. X. The Coordination Geometry of SO2 in Bis(phosphane)-Sulphur Dioxide-Nickel(0) Complexes. Structure of Ni(PCy3)2(SO2)The SO2 coordination geometry in Ni(PR3)2(SO2) complexes with steric parameters of the coligands Θ ≫ 141° was investigated by means of IR and 31P-NMR spectroscopy. The X-ray structure of Ni(PCy3)2(SO2) is described. The hitherto discussed n2-S.O-SO2 coordination mode for this type of complexes couldn't be confirmed.
    Notes: Zur Ermittlung der SO2-Koordinationsgeometrie in Ni(PR3)2(SO2)-Komplexen deren Coliganden Kegelöffnungswinkel von Θ ≫ 141° aufweisen, wurden die IR-und 31P-NMR-Spektroskopie herangezogen. Die Einkristallröntgenstrukturanalyse von Ni(PCy3)2(SO2) wird beschrieben. Eine für diesen Komplextyp bislang diskutierte n2-S.O-Koordination des Schwefeldioxids ließ sich nicht bestätigen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...