6363-19-5Relevant academic research and scientific papers
Molecular orientation of a new anthracene derivate for highly-efficient blue fluorescence OLEDs
Sohn, Sunyoung,Kim, Myeong-Jong,Jung, Sungjun,Shin, Tae Joo,Lee, Han-Koo,Kim, Yun-Hi
, p. 234 - 240 (2015)
A new anthracene derivative of 9,10-bis(2,5-dimethyl-4-(naphthalen-2-yl)phenyl)-2,3-diphenylanthracene (BDNPA) was designed and synthesized as a non-doped blue emitter in organic light emitting diodes (OLEDs). BDNPA has highly rigid structure and thermal
From enolates to anthraquinones
Bailey, David,Murphy, Jeffrey N.,Williams, Vance E.
, p. 659 - 666 (2007/10/03)
A series of highly reactive cyclopentadienones were prepared in situ from the corresponding hydroxycyclopent-2-enones and trapped with a variety of quinones. Reaction of 1,4-naphthoquinone with 4-hydroxy-3,4-diphenyl-cyclopent- 2-enone afforded 2,3-diphenylanthraquinone, whereas reaction of benzoquinone with this same cyclopentadienone precursor yielded a mixture of 6,7-dipheny 1-1,4-naphthoquinone and 2,3,6,7-tetraphenylanthraquinone. A number of other 2,3-diarylanthraquinones were likewise prepared in moderate yields from the reaction of 1,4-naphthoquinone with the appropriate 4-hydroxy-3,4- diarylcyclopent-2-enones. This method appears to be generally applicable to the synthesis of anthraquinone derivatives substituted at the 2- and 3-positions from inexpensive starting materials.
An efficient synthesis of substituted anthraquinones and naphthoquinones
Bailey, David,Williams, Vance E.
, p. 2511 - 2513 (2007/10/03)
An efficient synthesis of 6,7-disubstituted naphthoquinones and 2,3,6,7-tetrasubstituted anthraquinones were developed using the reaction of thiophene dioxides and benzoquinone and naphthoquinone derivatives, respectively.
