Institut des Sciences Chimiques de Rennes - UMR CNRS 6226, Université Rennes 1 , 35042 Rennes, France.
LPICM, CNRS, Ecole Polytechnique, Université Paris Saclay , 91128 Palaiseau, France.
ACS Appl Mater Interfaces. 2017 Feb 22;9(7):6194-6206. doi: 10.1021/acsami.6b14285. Epub 2017 Feb 8.
We report herein a detailed structure-properties relationship study of the first examples of electron-rich 4-substituted spirobifluorenes for organic electronic applications, namely, 4-phenyl-N-carbazole-spirobifluorene (4-PhCz-SBF) and 4-(3,4,5-trimethoxyphenyl)-spirobifluorene (4-Ph(OMe)-SBF). The incorporation of the electron-rich moieties in the ortho position of the biphenyl linkage (position C4) induces unique properties, very different from those previously described in the literature for this family of semiconductors. Both dyes can be readily synthesized, possess high triplet energies and excellent thermal stability, and their HOMO energy levels are highly increased compared to those of other 4-substituted SBFs. We also provide in this work the first rationalization of the peculiar fluorescence of 4-substituted SBFs. Finally, the present dyes have been successfully incorporated as host in green and blue phosphorescent organic light-emitting diodes with high performance either for the green (EQE of 20.2%) or the blue color (EQE of 9.6%). These performances are, to the best of our knowledge, among the highest reported to date for 4-substituted SBF derivatives.
我们在此报告了首例富电子 4-取代螺二芴在有机电子应用中的结构-性能关系的详细研究,即 4-苯基-N-咔唑螺二芴(4-PhCz-SBF)和 4-(3,4,5-三甲氧基苯基)-螺二芴(4-Ph(OMe)-SBF)。富电子部分在联苯连接的邻位(C4 位)的引入诱导出了独特的性质,与该族半导体以前在文献中描述的性质非常不同。两种染料都可以很容易地合成,具有高三重态能量和优异的热稳定性,与其他 4-取代 SBF 相比,它们的 HOMO 能级显著提高。我们还在这项工作中首次对 4-取代 SBF 荧光的奇特性质进行了合理化解释。最后,这些染料成功地作为主体掺入绿色和蓝色磷光有机发光二极管中,在绿色(EQE 为 20.2%)或蓝色(EQE 为 9.6%)方面表现出了优异的性能。就我们所知,这些性能是迄今为止报道的 4-取代 SBF 衍生物中的最高性能之一。