发光学报
髮光學報
발광학보
CHINESE JOURNAL OF LUMINESCENCE
2007年
6期
923-929
,共7页
罗艳%林崔昆%王振领%贾佩云%孙玉风%刘小明%林君%徐国跃
囉豔%林崔昆%王振領%賈珮雲%孫玉風%劉小明%林君%徐國躍
라염%림최곤%왕진령%가패운%손옥풍%류소명%림군%서국약
苝四酰二亚胺%微纤%自组装%光物理性质
苝四酰二亞胺%微纖%自組裝%光物理性質
패사선이아알%미섬%자조장%광물이성질
perylene diimide%microfiber%self-assembly%photophysical properties
在功能染料中,由于苝四酰二亚胺独特的光学及光物理性质,引起了人们广泛重视,但是制备一维苝四酰二亚胺结构尚是一种挑战.合成了二(正丁基)苝四酰二亚胺衍生物,通过对溶剂的选择,用自组装方法得到了其一维微纤结构,FESEM及TEM表明该微纤结构有1~2个微米宽,几百个微米长.XRD结果表明其内部结构高度有序.对其机理研究表明,苝四酰二亚胺核之间的π-π堆积和憎溶剂效应以及正丁基较小的空间位阻对微纤的形成起重要作用,由于微纤中苝四酰二亚胺分子的紧密堆积,引起苝四酰二亚胺核强烈的π-π相互作用使得苝四酰二亚胺激发态分子间电荷迁移作用增强,不论是其UV-Vis吸收光谱还是其发光光谱都有较大红移,其光学性能同相应的溶液比较有很大差别.苝四酰二亚胺在维度可控光电器件的应用方面提供了有益的实验数据,使其在光捕集系统、光电电池、场效应晶体管以及发光二级管的应用研究方面可能成为有前途的材料之一.
在功能染料中,由于苝四酰二亞胺獨特的光學及光物理性質,引起瞭人們廣汎重視,但是製備一維苝四酰二亞胺結構尚是一種挑戰.閤成瞭二(正丁基)苝四酰二亞胺衍生物,通過對溶劑的選擇,用自組裝方法得到瞭其一維微纖結構,FESEM及TEM錶明該微纖結構有1~2箇微米寬,幾百箇微米長.XRD結果錶明其內部結構高度有序.對其機理研究錶明,苝四酰二亞胺覈之間的π-π堆積和憎溶劑效應以及正丁基較小的空間位阻對微纖的形成起重要作用,由于微纖中苝四酰二亞胺分子的緊密堆積,引起苝四酰二亞胺覈彊烈的π-π相互作用使得苝四酰二亞胺激髮態分子間電荷遷移作用增彊,不論是其UV-Vis吸收光譜還是其髮光光譜都有較大紅移,其光學性能同相應的溶液比較有很大差彆.苝四酰二亞胺在維度可控光電器件的應用方麵提供瞭有益的實驗數據,使其在光捕集繫統、光電電池、場效應晶體管以及髮光二級管的應用研究方麵可能成為有前途的材料之一.
재공능염료중,유우패사선이아알독특적광학급광물이성질,인기료인문엄범중시,단시제비일유패사선이아알결구상시일충도전.합성료이(정정기)패사선이아알연생물,통과대용제적선택,용자조장방법득도료기일유미섬결구,FESEM급TEM표명해미섬결구유1~2개미미관,궤백개미미장.XRD결과표명기내부결구고도유서.대기궤리연구표명,패사선이아알핵지간적π-π퇴적화증용제효응이급정정기교소적공간위조대미섬적형성기중요작용,유우미섬중패사선이아알분자적긴밀퇴적,인기패사선이아알핵강렬적π-π상호작용사득패사선이아알격발태분자간전하천이작용증강,불론시기UV-Vis흡수광보환시기발광광보도유교대홍이,기광학성능동상응적용액비교유흔대차별.패사선이아알재유도가공광전기건적응용방면제공료유익적실험수거,사기재광포집계통、광전전지、장효응정체관이급발광이급관적응용연구방면가능성위유전도적재료지일.
Among functional dyes, perylene diimides have been of great interest due to their unique optical and photophysical properties. But the manipulation of superlong 1D structure of perylene diimides, however, is still a challenge. In this paper, superlong microfiber of bis(n-butyl) substituted perylene diimide (1) has been obtained by solvent evaporation method. FESEM and TEM micrographs indicate that the microfibers are 1~2 μm wide and several hundred micrometers long. XRD measurement demonstrates that the walls of the microfiber are arranged in highly ordered nanoscopic structure. Driving force for the formation of microfiber has been proposed, i. e., cooperation of solvophobic effect for molecules (1) and π-π stacking interaction between the perylene diimide cores. The effect of the closely packed structure on its photophysical behavior is demonstrated by the UV-Vis absorption and fluorescence spectra.