38701-90-5Relevant articles and documents
Organic electroluminescence devices based on anthracene sulfide derivatives
Nerungsi, Chakkrapan,Wanitchang, Piangkhwan,Sahasithiwat, Somboon,Sadorn, Karoon,Kerdcharoen, Teerakiat,Thongpanchang, Tienthong
, p. 6392 - 6395 (2010)
A series of anthracene derivatives are synthesized and fabricated as light-emitting materials in OLED devices. The incorporation of the chalcogen atoms, either oxygen or sulfur, in between the anthracene moiety and the alkyl or aryl substituents affected drastically the photo- and electroluminescence properties of the materials, especially the HOMO-LUMO band gap and the emitting color of the devices. The new anthracene sulfide derivatives represent a new design for further modification of other light-emitting doped materials.
Synthesis of Di-, Tri-, and tetrasulfides through multifold carbon-sulfur cross-coupling reactions with indium tri(organothiolates) in a one-pot procedure
Lee, Phil Ho,Park, Youngchul,Park, Sangkyun,Lee, Euijae,Kim, Sunggak
scheme or table, p. 760 - 765 (2011/04/15)
Pd-catalyzed multifold (2-, 3-, and 4-fold) carbon-sulfur cross-coupling reaction of indium tri(organothiolates) with polybromonated aromatic and heteroaromatic compounds was developed in a one-pot procedure. Both 2,5-dibromopyridine and 2,6-dibromopyridi
Through-bond interaction between sulfonium and sulfenyl sulfur atoms having anthracene and naphthalene spacers
Koyama, Emiko,Kobayashi, Kenji,Horn, Ernst,Furukawa, Naomichi
, p. 8833 - 8836 (2007/10/03)
The reaction of 9-(methylsulfinyl)-10-(methylthio)anthracene with trifluoroacetic anhydride followed by quenching with aqueous NaHCO3 gives 9,9-bis(methylthio)-10-anthraquinone. The dithia dication and/or the corresponding carbodication via thr
