13238-75-0Relevant articles and documents
Fluoranthene-based triarylamines as hole-transporting and emitting materials for efficient electroluminescent devices
Kapoor, Neha,Thomas, K. R. Justin
scheme or table, p. 2739 - 2748 (2011/02/18)
Electroluminescent materials based on the fluoranthene core and containing triarylamine segments were synthesized and characterized by IR, NMR, UV-Vis, and emission spectroscopic, electrochemical, and thermal studies. The electronic absorption and emissio
Synthesis of fluoranthenes and indenocorannulenes: Elucidation of chiral stereoisomers on the basis of static molecular bowls
Wu, Yao-Ting,Hayama, Tomoharu,Baldridge, Kim K.,Linden, Anthony,Siegel, Jay S.
, p. 6870 - 6884 (2007/10/03)
Cycloaromatization of a peri diyne with an external alkyne provides a general route to indenofused polynuclear aromatics. Fluoranthenes 9 (or 13) are easily accessible in good to excellent yields (75-99%; 18 examples) from the reaction of symmetric (or as
Novel perylene chromophores obtained by a facile oxidative cyclodehydrogenation route
Wehmeier, Mike,Wagner, Manfred,Muellen, Klaus
, p. 2197 - 2205 (2007/10/03)
New perylene chromophores, phenyl-substituted diindeno[1,2,3-cd: 1′,2′,3′-lm]perylenes 5a,b and 4,4′,7,7′-tetraphenyldiacenaphtho[1,2- k:1′,2′,k′]diindeno[1,2,3-cd:1′,2′,3′- me]perylenes 22a,b, have been synthesized from substituted fluoranthene derivatives 3 a,b and 4 a,b by means of a surprisingly simple oxidative cyclodehydrogenation reaction. The resulting chromophores, when substituted with alkyl chains at the periphery, show good solubility in organic solvents, and a full characterization of the novel red, green, and blue dyes by field-desorption mass spectrometry, UV/Vis and 1H and 13C NMR spectroscopy becomes possible.
