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萘基取代咔唑-喹啉轭合物中的热激活延迟荧光和室温磷光及其机械调控。

Thermally activated delayed fluorescence and room-temperature phosphorescence in naphthyl appended carbazole-quinoline conjugates, and their mechanical regulation.

机构信息

Department of Chemistry, Shiv Nadar University, NH-91, Tehsil Dadri, District Gautam Buddha Nagar, Uttar Pradesh, 201314, India.

出版信息

Chem Commun (Camb). 2019 Feb 7;55(13):1899-1902. doi: 10.1039/c8cc09220f.

DOI:10.1039/c8cc09220f
PMID:30657474
Abstract

The influences of naphthyl and/or phenyl rings at the 2,4-positions of the quinolinyl fragments in carbazole-quinoline conjugates are studied. The centric phase of one of the conjugates (β-CQNN) revealed both thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP), while prompt fluorescence and RTP were observed in the non-centric phase (α-CQNN) that can regenerate the emission features of β-CQNNvia mechanical grinding. This unique observation is explained by the modulation of the higher-lying triplet (T2) energy level caused by conformational change.

摘要

研究了咔唑-喹啉共轭物中喹啉片段的 2,4-位萘基和/或苯基环的影响。其中一个共轭物(β-CQNN)的中心相表现出热激活延迟荧光(TADF)和室温磷光(RTP),而在非中心相(α-CQNN)中则观察到了瞬间荧光和 RTP,通过机械研磨可以使非中心相恢复到β-CQNN 的发射特性。这种独特的观察结果可以通过构象变化引起的较高三重态(T2)能级的调制来解释。

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