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  • Dithiadiazolyl radicals  (1)
  • Electronic structure  (1)
  • dithiadiazolium salts  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2653-2656 
    ISSN: 0887-624X
    Keywords: dithiadiazolium salts ; initiators ; polymerization ; tetrahydrofuran ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mono-, bis- and tris-(1,3,2,4-dithiadiazolium) salts [R-(CNSNS+)n]n+[AsF-6]n (R = aryl, n = 1, 2, 3) were found to initiate the cationic ring-opening polymerization of tetrahydrofuran (THF) at room temperature to give clear gels from which the pure polymer was precipitated. 1,3,2,4-Dithiadiazolium cations associated with the hard [AsF6]- anion thus constitute a new class of cationic polymerization initiators. The poly(THF) formed by initiation with 1,3,2,4-dithiadiazolium cation was characterized by gel permeation chromatography, infrared spectrophotometry, and 13C-NMR spectroscopy. Number-average molecular weights of 198 700 g mol-1 (polydispersity 1.96) and 190 000 g mol-1 (polydispersity 1.61) were obtained using [PhCNSNS] [AsF6] and [C6H3-1,3,5-(CNSNS)3][AsF6]3, respectively, as initiators. The use of multifunctional dithiadiazolium salts as initiators suggests that they may be useful in the preparation of starburst and dendritic polymers. © 1992 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 487-491 
    ISSN: 0749-1581
    Keywords: ESR ; Dithiadiazolyl ; Diselenadiazolyl ; Metal complexation ; Electronic structure ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anisotropic ESR spectra (THF, frozen glass, 77 K) of PhCN2Se2· provide valuable information about the electronic structure of the diselenadiazolyl radical. Reaction of PhCN2Se2· with Pt(PPh3)3 in CH2Cl2 yielded the first diselenadiazolyl-metal complex, Pt[PhCN2Se2][PPh3]2. The electronic structures of both compounds are described in comparison with their sulphur analogues and the isoelectronic SN2E2+· radicals (E = S, Se).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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