630108-81-5Relevant articles and documents
Synthesis of rigid polycyclic secondary diamines: Bis-(2,3:6,7-iminodimethylene)anthracene and bis-(2,3:6,7-iminodimethylene)-9,10-dicarboxyethenoanthracene
Bhattacharyya, Sumita,Toftered, J?rgen,Nilsson, Ulf J.
, p. 1361 - 1363 (2003)
The synthesis of two rigid polycyclic secondary diamines, bis-(2,3:6,7-iminodimethylene)anthracene and bis-(2,3:6,7-iminodimethylene)-9,10-dicarboxyethenoanthracene, by means of Diels-Alder reaction between 1,2,4,5-tetra(dibromomethyl)benzene and maleimides followed by imide reduction, is described. Furthermore, these two cyclic secondary diamines undergo acylation with N-protected amino acids, thus providing functionalized, amphiphilic, and chiral building blocks for incorporation into supramolecular systems.
Anthracenedicarboximides as air-stable N-channel semiconductors for thin-film transistors with remarkable current on-off ratios
Wang, Zhiming,Kim, Choongik,Facchetti, Antonio,Marks, Tobin J.
, p. 13362 - 13363 (2008/04/11)
A new n-type semiconductor family for organic field-effect transistors (FETs), based on core-unsubstituted and core-cyanated anthracenedicarboximides, is reported. By tuning electron affinity, these materials exhibit good electron-transport properties and
