化工进展
化工進展
화공진전
CHEMICAL INDUSTRY AND ENGINEERING PROGRESS
2015年
7期
1941-1944,1955
,共5页
程清%文庆珍%王紫潇
程清%文慶珍%王紫瀟
정청%문경진%왕자소
电化学%烷烃%核磁共振%分子合成
電化學%烷烴%覈磁共振%分子閤成
전화학%완경%핵자공진%분자합성
electrochemistry%alkane%nuclear magnetic resonance(NMR)%molecular synthesis
基于丁氧基苯并硒二唑为电子受体,噻吩为电子给体的有机共轭分子通过斯蒂尔偶联反应制得,并对其进行结构表征和光电性能测试。结果表明:核磁共振1H 谱和13C 谱检测结果与理论一致;在乙腈溶液和聚甲基丙烯酸甲酯薄膜中,共轭分子有较宽的紫外吸收波长(237~464nm);荧光测得在红光区域有很强的激发峰,表明该分子是一种理想的红光材料;共轭分子(2.26~2.33eV)属于窄带隙,在电化学测试中表现出稳定的氧化还原曲线。以上结论表明该共轭分子在有机光电材料领域有潜在的应用价值。
基于丁氧基苯併硒二唑為電子受體,噻吩為電子給體的有機共軛分子通過斯蒂爾偶聯反應製得,併對其進行結構錶徵和光電性能測試。結果錶明:覈磁共振1H 譜和13C 譜檢測結果與理論一緻;在乙腈溶液和聚甲基丙烯痠甲酯薄膜中,共軛分子有較寬的紫外吸收波長(237~464nm);熒光測得在紅光區域有很彊的激髮峰,錶明該分子是一種理想的紅光材料;共軛分子(2.26~2.33eV)屬于窄帶隙,在電化學測試中錶現齣穩定的氧化還原麯線。以上結論錶明該共軛分子在有機光電材料領域有潛在的應用價值。
기우정양기분병서이서위전자수체,새분위전자급체적유궤공액분자통과사체이우련반응제득,병대기진행결구표정화광전성능측시。결과표명:핵자공진1H 보화13C 보검측결과여이론일치;재을정용액화취갑기병희산갑지박막중,공액분자유교관적자외흡수파장(237~464nm);형광측득재홍광구역유흔강적격발봉,표명해분자시일충이상적홍광재료;공액분자(2.26~2.33eV)속우착대극,재전화학측시중표현출은정적양화환원곡선。이상결론표명해공액분자재유궤광전재료영역유잠재적응용개치。
Organic conjugated molecule composed of central butoxybenzoselenadiazole (BseDZ) units as electron acceptor and thiophene groups as electron donors was prepared via the Stille coupling reaction. Structure and photoelectric properties of molecule were investigated. The test results of 1H NMR and 13C NMR were consistent with the theory. UV-vis spectroscopy showed that molecule had broad absorption spectrum (237—464nm) and its fluorescence spectra exhibited strong emission peaks in red light regions either in acetonitrile solution or in PMMA films,which illustrated that target molecule was ideal red light emission materials. The conjugated molecule(2.26eV to 2.33eV) belonged to narrow band gap and exhibited stable redox curve by cyclic voltammetry. The above conclusion suggested that it had a potential application in photoelectric material fields.