Red/NIR Thermally Activated Delayed Fluorescence from Aza-BODIPYs

被引:7
|
作者
Avellanal-Zaballa, Edurne [1 ]
Prieto-Castaneda, Alejandro [2 ]
Garcia-Garrido, Fernando [2 ]
Agarrabeitia, Antonia R. [2 ]
Rebollar, Esther [3 ]
Banuelos, Jorge [1 ]
Garcia-Moreno, Inmaculada [3 ]
Ortiz, Maria J. [2 ]
机构
[1] Univ Basque Country, Dept Quim Fis, UPV EHU, Aptdo 644, Bilbao 48080, Spain
[2] Univ Complutense, Dept Quim Organ, Ciudad Univ S-N, Madrid 28006, Spain
[3] CSIC, Dept Sistemas Baja Dimensionalidad Superficies &, Inst Quim FiS Rocasolano, IQFR, Serrano 119, Madrid 28006, Spain
关键词
charge transfer; delayed fluorescence; dye chemistry; energy transfer; NIR emission; PHOTOINDUCED ELECTRON-TRANSFER; MOLECULAR DESIGN; QUANTUM EFFICIENCY; EXCITED-STATE; DYAD; PET;
D O I
10.1002/chem.202002916
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The search for long-lived red and NIR fluorescent dyes is challenging and hitherto scarcely reported. Herein, the viability of aza-BODIPY skeleton as a promising system for achieving thermal activated delayed fluorescent (TADF) probes emitting in this target region is demonstrated for the first time. The synthetic versatility of this scaffold allows the design of energy and charge transfer cassettes modulating the stereoelectronic properties of the energy donors, the spacer moieties and the linkage positions. Delayed emission from these architectures is recorded in the red spectral region (695-735 nm) with lifetimes longer than 100 mu s in aerated solutions at room temperature. The computational-aided photophysical study under mild and hard irradiation regimes disclose the interplay between molecular structure and photonic performance to develop long-lived fluorescence red emitters through thermally activated reverse intersystem crossing. The efficient and long-lasting NIR emission of the newly synthesized aza-BODIPY systems provides a basis to develop advanced optical materials with exciting and appealing photonic response.
引用
收藏
页码:16080 / 16088
页数:9
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