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
Filter
  • Electron spin resonance spectroscopy  (1)
  • Iron-tungsten carbonyl  (1)
  • Isotropic spectra  (1)
  • 1
    ISSN: 0749-1581
    Keywords: ESR ; Isotropic spectra ; Powder spectra ; Dithiadiazolyl radicals ; Dimerization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solution and powder ESR spectra of the 4-trifluoromethyl-1,2,3,5-dithiadiazolyl and 4-pentafluorophenyl-1,2,3,5-dithiadiazolyl free radicals were analysed. Comparison of the ESR parameters with those obtained for the protonated equivalents shows that fluorination produces a drift of unpaired electron spin density away from the nitrogen 2px orbitals towards sulphur 3px orbitals (x is the direction perpendicular to the heterocyclic ring), consistent with an increase in electronegativity of the substituent. The fluorinated radicals dimerize more readily than their protonated counterparts.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0749-1581
    Keywords: Electron spin resonance spectroscopy ; Sulphur-nitrogen-containing radicals ; Dithiadiazolyl radicals ; Dithiadiazolyl radicals ; Dithiazophospholyl radicals ; Phosphaalkynes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Further information has been obtained on the electronic structure of 1,3,2-dithiazol-2-yl radicals. The structure has been well characterized previously except for positions 4 and 5 in the ring. We have obtained solution and powder ESR spectra of radicals substituted with 13C in both positions and of radicals substituted with nitrogen or phosphorus in the 4-position. It is probably the first time that a compound has been prepared containing the ring. Two especially interesting facts emerged from the ESR spectra of these 1,3,2-dithiazolyl radicals: the 13C-substituted radical has a considerable amount of p spin density in the plane of the ring and the phosphorussubstituted radical has a very low unpaired spin density at the phosphorus atom. It is known that 1,3,2,4-dithiadiazolyl radicals isomerize readily by photolysis to the symmetrical 2,3,1,4-dithiadiazolyl radicals; we attempted the same reaction with But and a new radical was produced that we have been unable to identify.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. 476-481 
    ISSN: 0749-1581
    Keywords: Electron paramagnetic resonance ; Electron spin resonance ; Metal carbonyl radical ; Iron-tungsten carbonyl ; Unpaired electron ; g Matrix ; Odd-electron carbonyl ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Single crystals of PPN+HFeW(CO)9- prepared from THF · W(CO)5 and PPN+HFe(CO)4- exhibit weak single-line EPR spectra corresponding to the presence of two paramagnetic impurities. One of the spectra increases in intensity by an order of magnitude on 60Co γ-irradiation. The g2 matrices for both species in an orthogonal crystal-axis system were assembled from measurements of g values made at 77 K on crystallographically oriented samples. The intense spectrum has principal g values of 2.0064, 2.0468 and 2.1320 and principal directions of g which lie close to bonds emanating from the Fe nucleus of the undamaged anion. Consideration of the principal g values and directions for this species leads to an assignment to a FeW(CO)9- radical in which the unpaired electron is principally located in a Fe 3dz2 orbital directed along the Fe—H bond of the host anion. The other signal has principal g values (2.0229, 2.0425, 2.0950) close to those established for the singly bridged isomer of Fe2(CO)8-, but their directions do not correlate well with bond directions within the host anion. It is concluded that small amounts of the persistent Fe2(CO)8- radical generated in the preparative procedures substitute for the host anion in the crystals of PPN+HFeW(CO)9-.
    Additional Material: 3 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...