70866-25-0Relevant academic research and scientific papers
Synthesis of Dibenzo[h,rst]pentaphenes and Dibenzo[fg,qr]pentacenes by the Chemoselective C-O Arylation of Dimethoxyanthraquinones
Suzuki, Yusuke,Yamada, Kohei,Watanabe, Kentaro,Kochi, Takuya,Ie, Yutaka,Aso, Yoshio,Kakiuchi, Fumitoshi
, p. 3791 - 3794 (2017/07/26)
A convenient method for the syntheses of dibenzo[h,rst]pentaphenes and dibenzo[fg,qr]pentacenes via the ruthenium-catalyzed chemoselective C-O arylation of 1,4- and 1,5-dimethoxyanthraquinones is described. Dimethoxyanthraquinones reacted selectively with
The electrochemistry of arylated anthraquinones in room temperature ionic liquids
Gomis-Berenguer, Alicia,Gomez-Mingot, Maria,Garcia-Cruz, Leticia,Thiemann, Thies,Banks, Craig E.,Montiel, Vicente,Iniesta, Jesus
, p. 367 - 375 (2013/05/21)
Arylated anthraquinone derivatives of different sizes and different π-basicities have been prepared, and the electrochemical behaviour of these substances has been studied on screen printed graphite electrodes in the three room temperature ionic liquids (RTILs), 1-butyl-3-methylimidazolium hexafluorophosphate ([C4MIM][PF6]), 1-hexyl-3- methylimidazolium hexafluorophosphate ([C6MIM][PF6]) and 1-octyl-3-methylimidazolium hexafluorophosphate ([C8MIM][PF 6]). Half redox potentials for the first and second one electron reduction waves were identified, and the diffusion coefficient values were estimated from cyclic voltammetry measurements. The influence of the nature of the RTIL and of the substitution pattern of the anthraquinone on the solvodynamic radii were studied. A correlation of the reductive potentials with the corresponding Hammett constants of the substituents was tested. Copyright
Brominated thiophenes as precursors in the preparation of brominated and arylated anthraquinones
Thiemann, Thies,Tanaka, Yasuko,Iniesta, Jesus
experimental part, p. 1013 - 1031 (2009/10/10)
Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended π-systems with interspersed anthraquinone units.
