Synthesis and Photophysical Properties of Conjugated Quinolines
2009 ◽
Vol 2009
(7)
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pp. 427-429
◽
Aryl halides were prepared by condensation of 2-methylquinoline and bromo- or chloro-arylaldehydes in acetic anhydride. Diarylamines reacted with the aryl halides to afford novel triarylamine derivatives using Pd(OAc)2/P ( o-tolyl)3 as catalyst. These compounds have potential as organic light-emitting device materials and were characterised by FT-IR, 1H NMR and elemental analyses. The UV-vis absorption and photoluminescent spectra of the compounds in CH2CI2 were investigated. The lowest absorption band of the triarylamine derivatives centred at about 400 nm was assigned to a charge-transfer transition with an emission at 500–515 nm.
2011 ◽
Vol 295-297
◽
pp. 373-377
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2012 ◽
Vol 229-231
◽
pp. 192-196
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Keyword(s):
2015 ◽
Vol 19
(10)
◽
pp. 1114-1122
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Keyword(s):
2011 ◽
Vol 239-242
◽
pp. 2612-2615