The present invention discloses synthesis of 2,2'-disubstituted 9,9'-spirobifluorene-based triaryldiamine. First, 2,2'-diamino-9,9'-spirobifluorene, a Pd-catalyst as auxiliary and aryl halide BX are provided, wherein X is selected from the group consisting of: Cl, Br and I, B comprises one of the following group: aryl moiety, hetero cycle, multiple fused ring, multiple fused ring with hetero atom(s). Next, a substitution reaction is performed to react the 2,2'-diamino-9,9'-spirobifluorene with the aryl halide BX to produce the 2,2'-disubstituted 9,9'-spirobifluorene-based triaryldiamines. In addition, the present invention discloses organic light emitting devices comprising hole transporting material comprising 2,2'-bis(N,N-disubstituted amino)-9,9'-spirobifluorenes.

 
Web www.patentalert.com

< 2,5-linked polyfluorenes for optoelectronic devices

< Light emitting element and light emitting device having the light emitting element

> Electroluminescent device with acetylacetonato complex salt included in phosphor layer

> Electroluminescent materials and devices

~ 00607