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2000
Volume 12, Issue 5
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A series of 2,6-bis(arylethynyl)anthraquinones was prepared via double Sonogashira coupling to 2,6-diiodoanthraquinone, and characterized with regard to their optical and electronic properties. Substitution with a derivatized phenylethynyl group produced a λonset of 366 nm (Eg = 3.4 eV), but the more highly conjugated 2,6-bis(9’-anthracylethynyl)anthraquinones exhibited a λonset of approximately 540 nm (Eg = 2.3 eV). Poor solubility in the unsubstituted 9’-anthracylethynyl system hampered complete characterization or purification, but the 10’-hexanoylanthrac-9’-ylethynyl analog exhibited significantly better solubility. The preparation of several other functionalized derivatives was also explored, and key synthetic findings are reported.

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/content/journals/loc/10.2174/1570178612666150203004458
2015-01-01
2025-09-26
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/content/journals/loc/10.2174/1570178612666150203004458
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  • Article Type:
    Research Article
Keyword(s): Anthraquinone; HOMO-LUMO gap; organic semiconductor; sonogashira coupling
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