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多环酰亚胺衍生物:通过分子工程合成及有效调节最低未占据分子轨道能级。

Polycyclic imide derivatives: synthesis and effective tuning of lowest unoccupied molecular orbital levels through molecular engineering.

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), the Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.

出版信息

Org Lett. 2010 Dec 3;12(23):5522-5. doi: 10.1021/ol1024103. Epub 2010 Nov 11.

Abstract

A series of fluoranthene-fused imide derivatives were facilely developed through a Diels-Alder reaction followed by decarbonylation. The investigation of their photophysical and electrochemical properties demonstrated that their LUMO levels were effectively tuned from -3.2 to -3.8 eV through the introduction of a fused imide unit, which provides a platform to design new air-stable and solution-processable n-type materials.

摘要

通过 Diels-Alder 反应和脱羰反应,简便地开发了一系列荧蒽稠合酰亚胺衍生物。对它们的光物理和电化学性质的研究表明,通过引入稠合酰亚胺单元,有效地调节了它们的 LUMO 能级,从-3.2 到-3.8 eV,这为设计新的空气稳定和溶液可加工的 n 型材料提供了一个平台。

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