1401967-47-2Relevant academic research and scientific papers
“N-alkyl diketopyrrolopyrrole-based fluorophores for luminescent solar concentrators: Effect of the alkyl chain on dye efficiency”
Lucarelli, Jonathan,Lessi, Marco,Manzini, Chiara,Minei, Pierpaolo,Bellina, Fabio,Pucci, Andrea
, p. 154 - 162 (2016)
We report on the preparation of luminescent solar concentrators (LSCs) made of poly(methyl methacrylate) (PMMA) thin films doped with six new diketopyrrolopyrrole (DPP) fluorophores obtained in good yields by using simple N-alkylation and direct C[sbnd]H
Solvent-Free Pd-Catalyzed Heteroaryl-Aryl Coupling via C-H Bond Activation for the Synthesis of Extended Heteroaromatic Conjugated Molecules
Punzi, Angela,Capozzi, Maria Annunziata M.,Di Noja, Simone,Ragni, Roberta,Zappimbulso, Nicola,Farinola, Gianluca M.
, p. 9312 - 9321 (2018/08/03)
Direct arylation of thienopyrrolodione, diketopyrrolopyrroles, benzodithiophene derivatives, and fluorinated heteroarenes with functionalized aryl iodides is proven in solvent-free and non-anhydrous conditions. The reaction is performed in the presence of air and tolerates several functional groups on both the coupling partners, enabling a convenient synthesis of extended heteroaromatic conjugated molecules.
Transition metal-catalyzed C-H activation as a route to structurally diverse di(arylthiophenyl)-diketopyrrolopyrroles
Zhang, Junxiang,Kang, Dun-Yen,Barlow, Stephen,Marder, Seth R.
supporting information, p. 21392 - 21394 (2013/01/15)
Dithiophenyldiketopyrrolopyrroles can be directly (hetero)arylated in moderate to excellent yields by Pd-catalyzed coupling to the CH position of a fluoro(hetero)arene (in the presence of Ag2CO3) or the CBr position of a bromo(hetero
