首页> 外文期刊>The Journal of Organic Chemistry >Core-perfluoroalkylated perylene diimides and naphthalene diimides: Versatile synthesis, solubility, electrochemistry, and optical properties
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Core-perfluoroalkylated perylene diimides and naphthalene diimides: Versatile synthesis, solubility, electrochemistry, and optical properties

机译:核心全氟烷基化per二酰亚胺和萘二酰亚胺:通用的合成方法,溶解性,电化学和光学性质

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By a strategy featuring perfluoroalkylation of the highly soluble intermediates and their further efficient transformations to target compounds, a versatile synthesis of core-perfluoroalkylated perylene diimides (PDIs) and naphthalene diimides (NDIs) was developed, and PDIs perfluoroalkylated at 1-position or 1,6-positions and core-perfluoroalkylated NDIs were first obtained. By esterification, perfluoroalkylation, hydrolysis, and condensation with amine, 1-perfluorooctyl-PDIs (7b, 7c, and 7e), 1,7-bis(perfluorooctyl)-PDIs (8a-c and 8e-g), 1,6-bis(perfluorooctyl)-PDIs (8-e), a mixture of 1,7-bis(trifluoromethyl)-PDIs and 1,6-bis(trifluoromethyl)-PDIs (11b and 11′b, 11d and 11′d, in a ratio of 19:1), 2-perfluorooctyl-NDIs (20a-d), and 2,6-bis(perfluorooctyl)-NDIs (21a-21d) were efficiently synthesized. Five valuable intermediates-1-perfluorooctylperylene dianhydride (5), 1,7-bis(perfluorooctyl)perylene dianhydride (6) 1,6-bis(perfluorooctyl) perylene dianhydride (6-), 2-perfluorooctylnaphthalene dianhydride (18), and 2,6-bis(perfluorooctyl) naphthalene dianhydride (19)-were also obtained, and they can condense with many amines to produce PDIs containing different functional side chains on the imide nitrogen atoms. Solubility, electrochemistry, and optical properties of the above core-perfluoroalkylated PDIs and NDIs were investigated. Core-perfluoroalkylated 8e, 8f, 8-e, mixture of 11d and 11′d, 20b, and 20d with excellent solubility in common organic solvents are competitive as candidates as solution processable semiconductors. Core-perfluoroalkylated PDIs and NDIs with experimental LUMO energy of 4.04-4.34 eV demonstrate strong electron accepting ability. For core-perfluoroalkylated PDIs, the maximum absorptions display blue shifts of 6-18 nm and the maximum molar extinction coefficients decrease obviously relative to those of unsubstituted PDIs, and they inherit the strong fluorescence from the PDIs family, which makes them promising fluorescent dyes.
机译:通过以高溶解度中间体的全氟烷基化及其进一步有效转化为目标化合物为特征的策略,开发了核全氟烷基化per二酰亚胺(PDI)和萘二酰亚胺(NDI)的通用合成方法,并将PDI在1位或1位全氟烷基化首先获得6-位和核心全氟烷基化的NDI。通过酯化,全氟烷基化,水解和与胺的缩合反应,可形成1-全氟辛基-PDI(7b,7c和7e),1,7-双(全氟辛基)-PDI(8a-c和8e-g),1,6-双(全氟辛基)-PDI(8-e),1,7-双(三氟甲基)-PDI和1,6-双(三氟甲基)-PDI(11b和11'b,11d和11'd)的混合物比例为19:1),2-全氟辛基-NDI(20a-d)和2,6-双(全氟辛基)-NDI(21a-21d)被有效地合成。五种有价值的中间体-1-全氟辛基per二酐(5),1,7-双(全氟辛基)per二酐(6)1,6-双(全氟辛基)per二酐(6-),2-全氟辛基萘二酐(18)和2还获得了6-6-双(全氟辛基)萘二酐(19),它们可以与许多胺缩合,生成在酰亚胺氮原子上包含不同官能侧链的PDI。研究了上述核心全氟烷基化的PDI和NDI的溶解度,电化学和光学性质。全氟烷基化的8e,8f,8-e核,11d和11'd的混合物,20b和20d在普通有机溶剂中具有极好的溶解性,作为可溶液加工的半导体具有竞争优势。实验LUMO能量为4.04-4.34 eV的核心全氟烷基化PDI和NDI显示出强大的电子接受能力。对于核心全氟烷基化的PDI,相对于未取代的PDI,最大吸收显示出6-18 nm的蓝移,并且最大摩尔消光系数明显降低,并且它们继承了PDI家族的强荧光,这使其成为有前途的荧光染料。

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