38257-52-2Relevant articles and documents
A new route towards fluorescent organic nanoparticles with red-shifted emission and increased colloidal stability
Amro, Kassem,Daniel, Jonathan,Clermont, Guillaume,Bsaibess, Talia,Pucheault, Mathieu,Genin, Emilie,Vaultier, Michel,Blanchard-Desce, Mireille
, p. 1903 - 1909 (2014)
Suzuki-Miyaura cross-coupling reaction with a new boron reagent has been used to conveniently and efficiently synthetize a dipolar chromophore having an elongated π-conjugated system (i.e., bithiophene based), which displays a red-shifted emission while m
Electron-Catalyzed Coupling of Magnesium Amides with Aryl Iodides
Kiriyama, Kazuya,Okura, Keisho,Tamakuni, Fumiko,Shirakawa, Eiji
supporting information, p. 4519 - 4522 (2018/03/13)
An electron was found to catalyze the coupling of magnesium diarylamides with aryl iodides giving triarylamines through a radical-anion intermediate. The transformation requires no transition metal catalysts or additives, and a wide array of products are formed in good-to-excellent yields.
ORGANIC LIGHT-EMITTING DIODE MATERIALS
-
Paragraph 0546, (2018/08/09)
Described herin are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moeity D, each moiety D is covalently attached to either the moeity B or the moeity A, and each B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D and B are defined herein.