Eder Simon, Ding Bowen, Thornton Daisy B, Sammut Darlene, White Andrew J P, Plasser Felix, Stephens Ifan E L, Heeney Martin, Mezzavilla Stefano, Glöcklhofer Florian
Department of Chemistry Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.
Centre for Processable Electronics Imperial College London Molecular Sciences Research Hub London W12 0BZ UK.
Angew Chem Weinheim Bergstr Ger. 2022 Nov 25;134(48):e202212623. doi: 10.1002/ange.202212623. Epub 2022 Oct 25.
Aromatic carboxylic anhydrides are ubiquitous building blocks in organic materials chemistry and have received considerable attention in the synthesis of organic semiconductors, pigments, and battery electrode materials. Here we extend the family of aromatic carboxylic anhydrides with a unique new member, a conjugated cyclophane with four anhydride groups. The cyclophane is obtained in a three-step synthesis and can be functionalised efficiently, as shown by the conversion into tetraimides and an octacarboxylate. Crystal structures reveal the high degree of porosity achievable with the new building block. Excellent electrochemical properties and reversible reduction to the tetraanions are shown for the imides; NMR and EPR measurements confirm the global aromaticity of the dianions and evidence the global Baird aromaticity of the tetraanions. Considering the short synthesis and unique properties, we expect widespread use of the new building block in the development of organic materials.
芳香族羧酸酐是有机材料化学中普遍存在的结构单元,在有机半导体、颜料和电池电极材料的合成中受到了广泛关注。在此,我们扩展了芳香族羧酸酐家族,引入了一个独特的新成员,即带有四个酸酐基团的共轭环芳。该环芳通过三步合成法获得,并且可以高效地进行官能化,转化为四酰亚胺和八羧酸盐即证明了这一点。晶体结构表明,这种新的结构单元可实现高度的孔隙率。酰亚胺显示出优异的电化学性能以及可逆还原为四价阴离子的特性;核磁共振(NMR)和电子顺磁共振(EPR)测量证实了二价阴离子的整体芳香性,并证明了四价阴离子的整体贝尔德芳香性。考虑到其简短的合成过程和独特的性质,我们预计这种新的结构单元将在有机材料的开发中得到广泛应用。