发光学报
髮光學報
발광학보
CHINESE JOURNAL OF LUMINESCENCE
2008年
4期
675-680
,共6页
李奋强%梁欣苗%张鑫%边建红%王煜%张昭
李奮彊%樑訢苗%張鑫%邊建紅%王煜%張昭
리강강%량흔묘%장흠%변건홍%왕욱%장소
亚胺%2,7-二溴芴酮%苯胺衍生物%荧光
亞胺%2,7-二溴芴酮%苯胺衍生物%熒光
아알%2,7-이추물동%분알연생물%형광
imino%2,7-dibromofluorenone%aniline derivatives%fluorescence
通过2,7-二溴芴酮与相应的苯胺衍生物反应,合成了一系列新型的含有亚胺基的芴类衍生物:2,7-二溴-9-亚苯胺基芴(NBFA),2,7-二溴-9-亚(4-氯-苯胺)基芴(CNBFA),2,7-二溴-9-亚(4-甲基-苯胺)基芴(MNBFA),其结构经氢核磁共振谱、红外光谱和质谱表征,并且采用紫外光谱法和荧光光谱法研究了这些化合物的光物理过程.
通過2,7-二溴芴酮與相應的苯胺衍生物反應,閤成瞭一繫列新型的含有亞胺基的芴類衍生物:2,7-二溴-9-亞苯胺基芴(NBFA),2,7-二溴-9-亞(4-氯-苯胺)基芴(CNBFA),2,7-二溴-9-亞(4-甲基-苯胺)基芴(MNBFA),其結構經氫覈磁共振譜、紅外光譜和質譜錶徵,併且採用紫外光譜法和熒光光譜法研究瞭這些化閤物的光物理過程.
통과2,7-이추물동여상응적분알연생물반응,합성료일계렬신형적함유아알기적물류연생물:2,7-이추-9-아분알기물(NBFA),2,7-이추-9-아(4-록-분알)기물(CNBFA),2,7-이추-9-아(4-갑기-분알)기물(MNBFA),기결구경경핵자공진보、홍외광보화질보표정,병차채용자외광보법화형광광보법연구료저사화합물적광물리과정.
The study on organic electroluminescence devices (OELDs) have become one of the fascinating fields recently. Compared with inorganic electroluminescence devices, OELDs possess excellent features such as high efficiency, high brightness, rich color, wide visual view, low energy consumption, fast response, low cost, low-voltage dri-ving matching integrate circuit, large-area full-color display, excellent mechanical properties and so on. As the foundation of OLEDs, organic electroluminescent(OEL) materials are one of the key factors influencing the device performance. Therefore, organic electroluminescent(OEL) materials are also one of chemists' hot subjects in this field. In this promising field, many chemists are devoting themselves to investigating the synthesis techniques and photophysical behaviors of new and excellent electroluminescent materials. At present, OELDs have made great progress and developed for practicality and commodity, but their properties still be in the need of improvement in brightness, efficiency, lifetime, etc. The fluorene derivatives containing imino groups, N-(2, 7-dibromo-9-flu-orenylidene)aniline(NBFA),4-methyl-N-(2,7-dibromo-9-fluorenylidene)aniline(MNBFA) and 4-chloro-N-(2, 7-dibromo-9-fluorenylidene)aniline(CNBFA) as novel organic electroluminescent compounds were synthesized by the reaction of 2,7-dibromofluorenone and corresponding aniline derivatives. The structures of the compounds were characterized by 1H NMR, IR and MS. The photophysical processes of the compounds were carefully investigated by UV-Vis absorption and fluorescence emission spectra. The results show that the emission spectra exhibited obvious solvent effects and functional group effects. The emitting intensities were quenched by diphenylketone(DPKT), a quencher of electron acceptor, and gradually decreased with the increase of quencher. The quenching effect followed the Stern-Volmer equation well. The imino derivatives (NBFA, CNBFA, MNBFA) of 2, 7-dibromofluorenone display not only a potential candidate as materials for organic electroluminescent devices, but also an intermediate for luminescent materials.