中山大学学报(自然科学版)
中山大學學報(自然科學版)
중산대학학보(자연과학판)
ACTA SCIENTIARUM NATURALIUM UNIVERSITATIS SUNYATSENI
2009年
6期
58-62,68
,共6页
张锡奇%杨志涌%陈美娜%许炳佳%张艺%池振国%许家瑞
張錫奇%楊誌湧%陳美娜%許炳佳%張藝%池振國%許傢瑞
장석기%양지용%진미나%허병가%장예%지진국%허가서
有机电致发光材料%联苯乙烯衍生物%合成%表征%液晶性
有機電緻髮光材料%聯苯乙烯衍生物%閤成%錶徵%液晶性
유궤전치발광재료%련분을희연생물%합성%표정%액정성
organic electroluminescent materials%distyrylarylene%synthesis%characterization%liquid crystalline property
联苯乙烯类衍生物被认为是一类具有实用价值的蓝光电致发光材料,它具有较优异的综合性能.以联苯乙烯为基础,利用Wittig-Horner反应分别引入N-己基吩噻嗪和N-己基咔唑基团,合成了两种联苯乙烯衍生物.利用核磁共振氢谱(~1H NMR)、傅立叶红外光谱(FT-IR)、质谱(MS)和元素分析(EA)对所合成产物进行了化学结构的表征;利用紫外吸光光度法(UV)、荧光分光光度法(PL)、热重分析(TGA)、示差扫描量热法(DSC)、热台偏光显微镜(PLM)和X-射线衍射(XRD)对产物的性能进行了初步的表征.结果表明:所合成的两个化合物在紫外光激发下均能发射高亮度荧光;具有较高的热稳定性;两个化合物均不能结晶,易溶于二氯甲烷等有机溶剂,并且容易成膜,非常适合于旋涂法制备OLED器件;其中含吩噻嗪基的化合物在熔融或冷却过程中均能观察到近晶A型液晶织构.
聯苯乙烯類衍生物被認為是一類具有實用價值的藍光電緻髮光材料,它具有較優異的綜閤性能.以聯苯乙烯為基礎,利用Wittig-Horner反應分彆引入N-己基吩噻嗪和N-己基咔唑基糰,閤成瞭兩種聯苯乙烯衍生物.利用覈磁共振氫譜(~1H NMR)、傅立葉紅外光譜(FT-IR)、質譜(MS)和元素分析(EA)對所閤成產物進行瞭化學結構的錶徵;利用紫外吸光光度法(UV)、熒光分光光度法(PL)、熱重分析(TGA)、示差掃描量熱法(DSC)、熱檯偏光顯微鏡(PLM)和X-射線衍射(XRD)對產物的性能進行瞭初步的錶徵.結果錶明:所閤成的兩箇化閤物在紫外光激髮下均能髮射高亮度熒光;具有較高的熱穩定性;兩箇化閤物均不能結晶,易溶于二氯甲烷等有機溶劑,併且容易成膜,非常適閤于鏇塗法製備OLED器件;其中含吩噻嗪基的化閤物在鎔融或冷卻過程中均能觀察到近晶A型液晶織構.
련분을희류연생물피인위시일류구유실용개치적람광전치발광재료,타구유교우이적종합성능.이련분을희위기출,이용Wittig-Horner반응분별인입N-기기분새진화N-기기잡서기단,합성료량충련분을희연생물.이용핵자공진경보(~1H NMR)、부립협홍외광보(FT-IR)、질보(MS)화원소분석(EA)대소합성산물진행료화학결구적표정;이용자외흡광광도법(UV)、형광분광광도법(PL)、열중분석(TGA)、시차소묘량열법(DSC)、열태편광현미경(PLM)화X-사선연사(XRD)대산물적성능진행료초보적표정.결과표명:소합성적량개화합물재자외광격발하균능발사고량도형광;구유교고적열은정성;량개화합물균불능결정,역용우이록갑완등유궤용제,병차용역성막,비상괄합우선도법제비OLED기건;기중함분새진기적화합물재용융혹냉각과정중균능관찰도근정A형액정직구.
Distyrylarylene derivative is one of the most promising blue OLED materials with good film forming ability and high thermal stability. Two compounds were synthesized by introducing the conjugated groups to the distyrylarylene backbone by using Wittig-Horner reactions. Their chemical structures were characterized by ~1H NMR, IR, MS and EA analyses, and the properties were investigated by UV, PL, TGA, DSC, PLM and XRD analyses. The results showed that (1) two compounds emitted strong fluorescence , and the emitting strength of the compound with phenothiazine structure was stronger than that with carbazole structure; (2) the compounds possessed high thermal stability; (3) the compounds had good solubility in organic solvents and film forming ability, which was advantaged for OLED device fabrication using spin-coating method; (4) the compound containing phenothiazine groups exhibited a Smectic A liquid crystalline phase under hot-stage PLM.