Dearomatizing [4+1] Spiroannulation of Naphthols: Discovery of Thermally Activated Delayed Fluorescent Materials. (21st January 2021)

• Record Type: Journal Article
• Authors: Liang, Wenbo; Yang, Yudong; Yang, Mufan; Zhang, Min; Li, Chengming; Ran, You; Lan, Jingbo; Bin, Zhengyang; You, Jingsong
• Is Part Of: Angewandte Chemie. Volume 133:Number 7(2021)
• Page Start: 3535
• Page End: 3539
• Publication Date: 2021-01-21
• Subjects: annulations -- C−H activation -- dearomatization -- fluorescence -- spiro-compounds; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.202012842
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Disclosed here is a palladium‐catalyzed direct [4+1] spiroannulation of ortho ‐C−H bonds of naphthols with cyclic diaryliodonium salts to construct spirofluorenyl naphthalenones (SFNP) under mild reaction conditions. This spiroannulation directly transforms the hydroxy group into a carbonyl group, and also tolerates reactive functional groups such as the halo groups, which provide an opportunity to rapidly assemble structurally new thermally activated delayed fluorescent (TADF) materials that feature a carbonyl group with an adjacent spirofluorenyl unit as the acceptor. As an illustrated example, the OLED device utilizing the assembled DMAC‐SFNP as the host material exhibits a low turn‐on voltage of 2.5 V and an ultra‐high external quantum efficiency of 32.2 %. This work provides inspiration for structurally new TADF materials, and also displays the potential of C−H activation as a synthetic strategy for the innovation of optoelectronic materials. Abstract : A dearomatizing [4+1] C−H spiroannulation of naphthols with cyclic diaryliodonium salts has been developed to rapidly deliver spirofluorenyl naphthalenones, which unlocks an opportunity to discover structurally new thermally activated delayed fluorescent (TADF) materials.