School of Materials Science and Engineering, Nanyang Technological University , Singapore 639798, Singapore.
J Org Chem. 2014 May 16;79(10):4438-45. doi: 10.1021/jo500400d. Epub 2014 Apr 25.
Three novel diazatwistpentacenes (1,4,6,13-tetraphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (1, IUPAC name: 9,11,14,16-tetraphenyl-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); 1,4-di(pyridin-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (2, IUPAC name: 9,16-diphenyl-11,14-di(pyridin-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); and 1,4-di(thien-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (3, IUPAC name: 9,16-diphenyl-11,14-di(thien-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine)) have been successfully synthesized through [4 + 2] cycloaddition reaction involving in situ arynes as dienophiles and substituted 1,2,4,5-tetrazines as dienes. Their structures have been determined by single-crystal X-ray diffraction, confirming that all compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diazaanthrance part as high as 21.52° (for 1), 24.74° (for 2), and 21.14° (for 3). The optical bandgaps for all compounds corroborate the values derived from CV. The calculation done by DFT shows that the HOMO-LUMO bandgaps are in good agreement with experimental data. Interestingly, the substituted groups (phenyl, pyridyl, thienyl) in the 1,4-positions did affect their self-assembly and the optical properties of as-resulted nanostructures. Under the same conditions, compounds 1-3 could self-assemble into different morphologies such as microrods (for 1), nanoprisms (for 2), and nanobelts (for 3). Moreover, the UV-vis absorption and emission spectra of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all materials. Surprisingly, both 1 and 2 showed aggregation-induced emission (AIE) effect, while compound 3 showed aggregation-caused quenching (ACQ) effect. Our method to approach novel twisted azaacenes through [4 + 2] reaction could offer a new tool to develop unusual twisted conjugated materials for future optoelectronic applications.
三种新型二氮杂并薁并戊烯(1,4,6,13-四苯基-7:8,11:12-双苯并-2,3-二氮杂并薁并戊烯(1,IUPAC 名称:9,11,14,16-四苯基-1,6-二氢苯并[8,9]三苯基并[2,3-g]酞嗪);1,4-二(吡啶-2-基)-6,13-二苯基-7:8,11:12-双苯并-2,3-二氮杂并薁并戊烯(2,IUPAC 名称:9,16-二苯基-11,14-二(吡啶-2-基)-1,6-二氢苯并[8,9]三苯基并[2,3-g]酞嗪);和 1,4-二(噻吩-2-基)-6,13-二苯基-7:8,11:12-双苯并-2,3-二氮杂并薁并戊烯(3,IUPAC 名称:9,16-二苯基-11,14-二(噻吩-2-基)-1,6-二氢苯并[8,9]三苯基并[2,3-g]酞嗪))已通过[4 + 2]环加成反应成功合成,其中涉及原位芳炔作为双烯体和取代的 1,2,4,5-四嗪作为二烯体。它们的结构通过单晶 X 射线衍射确定,证实所有化合物都具有扭曲构型,芘单元和 2,3-二氮杂薁部分之间的扭转角高达 21.52°(1)、24.74°(2)和 21.14°(3)。所有化合物的光学带隙与 CV 得出的值相符。DFT 计算表明,HOMO-LUMO 带隙与实验数据吻合良好。有趣的是,1,4-位的取代基(苯基、吡啶基、噻吩基)确实影响了它们的自组装和所得纳米结构的光学性质。在相同条件下,化合物 1-3 可以自组装成不同的形态,如微棒(1)、纳米棱柱(2)和纳米带(3)。此外,制备的纳米结构的紫外-可见吸收和发射光谱都发生了很大的红移,表明所有材料均为 J 型聚集。令人惊讶的是,1 和 2 都表现出聚集诱导发射(AIE)效应,而化合物 3 则表现出聚集诱导猝灭(ACQ)效应。我们通过[4 + 2]反应接近新型扭曲氮杂薁的方法为开发未来用于光电应用的不寻常扭曲共轭材料提供了一种新工具。