Library

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1038-1046 
    ISSN: 0044-2313
    Keywords: Binuclear antimony(V) complexes ; structure ; dynamics ; NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: d, h-μ-Benzylalkoxophosphonato-e-μ-alkoxo-f-μ-oxo-bis[trichloroantimony(V)] CompoundsThe binuclear antimony(V) complexes Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 - 6 with R1 = R2 = CH3, C2H5 and R3 = C6H5CH2, (CH3)3C6H2CH2 in solution slowly exchanges the R2 groups between the oxygen atoms of the Sb2O2 ring. The SbOPOSb ringsystem makes rapid pseudorotation. The isomeres are detected by nmr spectroscopy. 1 (R1 = R2 = CH3) crystallizes in the orthorhombic space group Pnma with a = 1247.0, b = 1324.1, c = 1207.9 pm and Z = 4. 2 (R1 = CH3, R2 = C2H5) and 5 (R1 = R2 = CH3, R3 = (CH3)3 · C6H2CH2) crystallizes triclinic in the space group P-1 with a = 984.1, b = 1026.7, c = 1079.9 pm, α = 87.93, β = 75.70, γ = 87.62° and Z = 2 and a = 1164.6, b = 1296.9, c = 1712.9 pm, α = 109.9, β = 96.3, γ = 100.2° and Z = 4 resp., with two crystallographically independent molecules in the asymmetric unit.
    Notes: Die zweikernigen Antimon(V)-Komplexe Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 bis 6 mit R1 = R2 = CH3, C2H5 und R3 = C6H5CH2, (CH3)3C6H2CH2 tauschen bei RT in Lösung langsam die R2-Gruppen aus. Daneben erfolgt rasches Umklappen des SbOPOSb-quasi-Fünfringes. Die Isomerenbildung wird NMR-spektroskopisch nachgewiesen. 1 (R1 = R2 = CH3) kristallisiert orthorhombisch in der Raumgruppe Pnma mit a = 1247,0, b = 1324,1, c = 1207,9 pm und Z = 4. 2 (R1 = CH3, R2 = C2H5) und 5 (R1 = R2 = CH3, R3 = (CH3)3C6H2CH2) kristallisieren triklin in der Raumgruppe P-1 mit a = 984,1, b = 1026,7, c = 1079,9 pm, α = 87,93, β = 75,70, γ = 87,62° und Z = 2 bzw. a = 1164,6, b = 1296,9, c = 1712,9 pm, α = 109,9, β = 96,3, γ = 100,2° und Z = 4 mit zwei kristallographisch unabhängigen Molekülen in der asymmetrischen Einheit.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1799-1804 
    ISSN: 0044-2313
    Keywords: 1,4,2λ5,5λ5-Dioxadiphosphorinane ; NMR spectra ; Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: P,P′-(2,5-Dihydroxy-3,6-dimethyl-2,5-dioxo-2λ5,5λ5-[1,4,2,5]dioxadiphosphinane-2,5-diyl)-bis-phosphonic AcidThe tetrahydrate 1 of the title compound crystallizes in the monoclinic space group P21/c with a = 845.8, b = 1 098, c = 981.7 pm, β = 113.02° and Z = 2. The anions of the oxonium compound (H3O+ · H2O)2(C4H10O12P42-) are layered by hydrogen bridges. The 1H, 13C and 31P NMR spectra (4 and 5 spin systems) are discussed.
    Notes: C4H12O12P4 · 4 H2O (1), das Tetrahydrat der Titelverbindung, kristallsiert monoklin in der Raumgruppe P21/c mit a = 845,8, b = 1 098, c = 981,7 pm, β = 113,02° und Z = 2. 1 liegt als Oxoniumsalz (H3O+ · H2O)2(C4H10O12P42-) vor, in dem die Anionen über H-Brücken zu Schichten verknüpft sind. Die 4- und 5-Spinsysteme der 1H-, 13C- und 31P-NMR-Spektren werden detailliert analysiert.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...