19219-82-0Relevant academic research and scientific papers
Redox-Active Heteroacene Chromophores Derived from a Nonlinear Aromatic Diimide
Luo, Stella M.,Stellmach, Kellie A.,Ikuzwe, Stella M.,Cao, Dennis D.
, (2019)
This work describes a three-step chromatography-free protocol for the synthesis of a novel organic materials building block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitution with a variety of ortho disubstituted
Redox-Active Heteroacene Chromophores Derived from a Nonlinear Aromatic Diimide
Luo, Stella M.,Stellmach, Kellie A.,Ikuzwe, Stella M.,Cao, Dennis D.
, p. 10362 - 10370 (2019/09/04)
This work describes a three-step chromatography-free protocol for the synthesis of a novel organic materials building block, dichlorinated mellophanic diimide (MDI), that is shown to undergo nucleophilic substitution with a variety of ortho disubstituted
Halogenation Using Quaternary Ammonium Polyhalides. XIX. Aromatic Chlorination of Arenes with Benzyltrimethylammonium Tetrachloroiodate
Kajigaeshi, Shoji,Ueda, Yasuhiro,Fujisaki, Shizuo,Kakinami, Takaaki
, p. 2096 - 2098 (2007/10/02)
The reaction of arenes with a calculated amount of benzyltrimethylammonium tetrachloroiodate in acetic acid at room temperature or at 70 deg C gave nuclear chloro-substituted arenes in fairly good yields.
ATTEMPTS TO POLYLITHIATE TETRABROMOARENES. THE COMPATIBILITY OF METHYL SULFATE AND BUTYLLITHIUM
Nwokogu, Godson C.,Hart, Harold
, p. 5725 - 5726 (2007/10/02)
Tetrabromo-o- and p-dichlorobenzenes are only dilithiated, even with excess n-butyllithium, although more than two bromines are replaced by methyl groups when such solutions are treated with methyl sulfate.
