苯并呋喃
窄带
分子内力
光电子学
材料科学
荧光
二极管
化学
基质(水族馆)
分子间力
区域选择性
有机发光二极管
光化学
组合化学
荧光粉
计算机科学
电子工程
激发态
纳米技术
反应条件
激发
作者
Guopeng Huang,Xiaoyu Guo,Xihao Yang,Jingsheng Miao,He Liu,Chuluo Yang
摘要
A metal-free amino-group-directed regioselective cyclization from α-diketone compounds and diarylamines is reported for the synthesis of benzofuran derivatives. The transformation proceeds through sequential intermolecular and intramolecular Friedel-Crafts-type processes under acidic conditions, enabling one-pot construction of fused benzofuran frameworks. The method shows good substrate scope, providing products in moderate yields and demonstrating gram-scale practicality. Based on this scaffold, two donor units are developed and incorporated into multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters, namely BNFFA and BNFFC. Both compounds exhibit narrowband emission (full with at half maximum = 20 and 25 nm) and decent delayed fluorescence. Organic light-emitting diodes based on these emitters achieved maximum external quantum efficiencies of 23.5% and 29.3%, with blue-cyan emissions suitable for emerging four-primary wide-color-gamut displays.
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