115228-92-7Relevant articles and documents
Understanding the desulphurization process in an ionic porous aromatic framework
Tian, Yuyang,Song, Jian,Zhu, Youliang,Zhao, Huanyu,Muhammad, Faheem,Ma, Tingting,Chen, Mo,Zhu, Guangshan
, p. 606 - 613 (2019)
An ionic porous aromatic framework, iPAF-1, was successfully synthesized from a designed monomer with imidazolium functional groups. The iPAF-1 exhibits the highest dibenzothiophene uptake among all reported adsorptive desulphurization adsorbents. The so-
Synthesis of tetraarylmethanes via a Friedel-Crafts cyclization/desulfurization strategy
Griffin, Paul J.,Fava, Matthew A.,Whittaker, St. John T.,Kolonko, Kristopher J.,Catino, Arthur J.
, p. 3999 - 4002 (2018/10/02)
Tetraarylmethanes are an important class of molecules that contain four aryl groups bonded to a central carbon atom. The shape/three-dimensionality of these molecules makes them suitable for organic light-emitting diodes (OLEDs), organic solar cells, hydrogen storage, and even drug-delivery. Despite their importance, there are only a few methods available for their preparation. Herein, we report a simple procedure for the preparation of tetraarylmethanes that involves a bismuth-catalyzed Friedel-Crafts cyclization followed by a desulfurization reaction mediated by Raney nickel.
