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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1403-1409 
    ISSN: 0009-2940
    Keywords: Paracyclothiophenophane ; Photodesulfurization ; Pyrolysis ; Reductive ring opening reaction ; [n] Paracyclophane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dithia[3]paracyclo[3](2,4)- and -(2,5)thiophenophanes 〈dithia-[3.3](2,4)- and -(2.5)PTP〉 (3, 7, 9) are obtained by the coupling reaction of the corresponding bis(chloromethyl)- and bis(mercaptomethyl)arenes. Desulfurization of the dithia[3.3]PTPs 3, 7, 9 by photolysis affords the thia[2.3]PTPs 15, 16, 17 and [2.2]PTPs 14, 18, 19, 20 The pyrolysis of the disulfone 12 gives the symmetrical thiophenophane 13. The dynamics of the ring inversion, the UV spectra, and the reductive ring opening with Raney-Ni (W-7) of the obtained PTPs are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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