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用于蓝色磷光的共价键合的原子尺度调控

Atomic-Scale Regulation of Covalent Bonding for Blue Phosphorescence.

作者信息

Gao Shuo, Yang Yongpeng, Wang Yan, Jiu Lianchao, Li Kaitao, Tian Rui, Lu Chao

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Pingyuan Laboratory, College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.

出版信息

Small. 2025 Jul;21(26):e2502227. doi: 10.1002/smll.202502227. Epub 2025 May 7.

Abstract

It is a long-standing challenge to construct blue room-temperature phosphorescence (RTP) materials due to the inevitable intermolecular conjugation and red-shifted emission of chromophores. In this work, layered double hydroxides (LDHs) are employed to confine the boronic acid-containing chromophores and modulate the competitive covalent reactions between chromophores to achieve blue RTP materials. Interestingly, the self-condensation of chromophores and co-condensation between chromophore-LDHs can be effectively altered by tuning the atomically dispersed trivalent metals in the LDHs. Accordingly, blue emissive and dynamic phosphorescence from blue to cyan are achieved. The as-prepared RTP materials are successfully applied for the multi-level anti-counterfeiting. The developed strategy can provide a deep understanding of the regulation of the competitive reaction and molecular arrangement of chromophores. It is anticipated that this approach can be further extended for diverse reaction regulation and molecular engineering for the multi-functional RTP materials.

摘要

由于发色团不可避免的分子间共轭和红移发射,构建蓝色室温磷光(RTP)材料一直是一项长期挑战。在这项工作中,层状双氢氧化物(LDHs)被用于限制含硼酸发色团,并调节发色团之间的竞争性共价反应,以实现蓝色RTP材料。有趣的是,通过调整LDHs中原子分散的三价金属,可以有效地改变发色团的自缩合以及发色团与LDHs之间的共缩合。相应地,实现了从蓝色到青色的蓝色发射和动态磷光。所制备的RTP材料成功应用于多级防伪。所开发的策略可以深入理解发色团竞争反应和分子排列的调控。预计这种方法可以进一步扩展到多功能RTP材料的各种反应调控和分子工程中。

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