Solid-state highly fluorescent diphenylaminospirobifluorenylfumaronitrile red emitters for non-doped organic light-emitting diodes.

Bright (maximum 11,000 cd m(-2) and 500 cd m(-2) at 20 mA cm(-2)) and efficient (maximum external quantum efficiency of 3.1% at 1 mA cm(-2)) red (CIE, x = 0.66, y = 0.34) organic light-emitting diodes (OLEDs) employ arylaminospirobifluorene-substituted fumaronitriles as the novel non-dopant red emitter.

Novel carbazole/fluorene hybrids: host materials for blue phosphorescent OLEDs.

[reaction: see text] A series of carbazole/fluorene (CBZm-Fn) hybrids were effectively synthesized through Friedel-Crafts-type substitution of the carbazole rings. These compounds were thermally and morphologically stable host materials for OLED applications. Efficient blue phosphorescent OLEDs were obtained when employing CBZ1-F2 as the host and FIrpic as the guest.

Improved synthesis of 2,2'-dibromo-9,9'-spirobifluorene and its 2,2'-bisdonor-7,7'-bisacceptor-substituted fluorescent derivatives.

Pure 2,2'-Dibromo-9,9'-spirobifluorene was synthesized by a method that did not involve troublesome dibromination of 9,9'-spirobifluorene or Sandmeyer reaction of 2,2'-diamino-9,9'-spirobifluorene. A series of donor-acceptor orthogonally substituted 9,9'-spirobifluorene was subsequently prepared showing rich variation of fluorescence in solution and in solid state. [reaction: see text]

Ortho-substituent effect on fluorescence and electroluminescence of arylamino-substituted coumarin and stilbene.

[structure: see text] Newly synthesized arylamino-substituted coumarins and stilbenes show enhanced fluorescence emission (bluer and brighter) both in solution and in solid film. Pure blue efficient electroluminescence with 2.7% and 4.1% of external quantum efficiency can be achieved with MeC1 and XTPS, respectively.