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发射可调谐的B←N路易斯对功能化萘

Emission-Tunable B←N Lewis Pair-Functionalized Naphthalenes.

作者信息

Zhang Yufeng, Matler Alexander, Krebs Johannes, Krummenacher Ivo, Ye Qing, Braunschweig Holger, Marder Todd B, Ji Lei

机构信息

Frontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE) & Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University, Xi'an, 710072, China.

Institute for Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.

出版信息

Chemistry. 2025 Feb 6;31(8):e202403973. doi: 10.1002/chem.202403973. Epub 2024 Dec 12.

Abstract

Herein, we simultaneously synthesized three different double B←N Lewis pair-functionalized naphthalenes including the asymmetric BNNY and BNNO and the mirror-symmetric BNNR, via a one-pot method. The annulation modes of the B←N Lewis pairs and the substituents on the boron atoms efficiently tune the molecular frontier orbitals and emission colors. α-Position fusion leads to a significant enhancement of the HOMO energy level and a decrease in the HOMO-LUMO gap, while the electron-withdrawing groups attached to the boron atom make the LUMO energy level more stable. In particular, the LUMO energy level of BNNO is as low as -3.12 eV. BNNY, BNNO, and BNNR emit cyan, green, and red fluorescence at 509, 534, and 620 nm, respectively, with fluorescence quantum yields of 24 %, 49 %, and 30 %, respectively.

摘要

在此,我们通过一锅法同时合成了三种不同的双B←N路易斯对功能化萘,包括不对称的BNNY和BNNO以及镜像对称的BNNR。B←N路易斯对的环化模式和硼原子上的取代基有效地调节了分子前沿轨道和发射颜色。α-位融合导致HOMO能级显著提高,HOMO-LUMO能隙减小,而连接在硼原子上的吸电子基团使LUMO能级更稳定。特别地,BNNO的LUMO能级低至-3.12 eV。BNNY、BNNO和BNNR分别在509、534和620 nm处发射青色、绿色和红色荧光,荧光量子产率分别为24%、49%和30%。

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