131268-46-7Relevant articles and documents
Heteroarylation of anthraquinone-triflate by Suzuki cross-coupling
Coudret, Christophe,Mazenc, Valerie
, p. 5293 - 5296 (1997)
The reactivity of the 4-pyridylboronate 5a for PdCl2(dppf)catalysed cross-coupling reaction with an anthraquinone triflate is presented, and compared with its 2-thienyl- and phenylboronic analogues. Best results have been obtained on a small sc
2,6-Diaryl-9,10-anthraquinones as models for electron-accepting polymers
Gautrot, Julien E.,Hodge, Philip,Cupertino, Domenico,Helliwell, Madeleine
, p. 1585 - 1593 (2007)
Anthraquinone derivatives have been little used in microelectronics though they are attractive scaffolds due to their electron-accepting properties. As part of a preliminary study, a series of conjugated anthraquinone derivatives has been synthesised. The
ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME
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Page/Page column 21-22, (2010/02/11)
An anthracene derivative represented by the following general formula (1) which enables an organic electroluminescence device to exhibit a great efficiency of light emission and uniform light emission even at high temperatures since crystallization is suppressed and no thermal decomposition takes place during vapor deposition and an organic electroluminescence device utilizing the derivative, are provided. [Ar represents a group represented by the following general formula (2): (L1 and L2 each represent a substituted or unsubstituted methylene group, ethylene group or the like, and at least one of them is present), Ar' represents a substituted or unsubstituted aryl group having 6 to 50 nuclear carbon atoms, X represent an alkyl group or the like, a and b each represent an integer of 0 to 4, and n represents an integer of 1 to 3.]