Author
Listed:
- Dan Tian
(Nanjing Tech University (NanjingTech))
- Fen Qi
(Nanjing Tech University (NanjingTech))
- Huili Ma
(Nanjing Tech University (NanjingTech))
- Xiaoqing Wang
(Nanjing Tech University (NanjingTech))
- Yue Pan
(Nanjing Tech University (NanjingTech))
- Runfeng Chen
(Nanjing University of Posts & Telecommunications)
- Zhen Shen
(Nanjing University)
- Zhipeng Liu
(Nanjing Tech University (NanjingTech))
- Ling Huang
(Nanjing Tech University (NanjingTech))
- Wei Huang
(Nanjing Tech University (NanjingTech)
Nanjing University of Posts & Telecommunications)
Abstract
Considerable achievements on multiple emission capabilities and tunable wavelengths have been obtained in inorganic luminescent materials. However, the development of organic counterparts remains a grand challenge. Herein we report a series of 2-/2,6-aryl substituted boron-dipyrromethene dyes with wide-range and multi-fluorescence emissions across red and near infrared in their aggregation states. Experimental data of X-ray diffraction, UV–vis absorption, and room temperature fluorescence spectra have proved the multiple excitation and easy-adjustable emission features in aggregated boron-dipyrromethene dyes. Temperature-dependent and time-resolved fluorescence studies have indicated a successive energy transfer from high to step-wisely lower-located energy levels that correspond to different excitation states of aggregates. Consistent quantum chemical calculation results have proposed possible aggregation modes of boron-dipyrromethene dyes to further support the above-described scenario. Thus, this study greatly enriches the fundamental recognition of conventional boron-dipyrromethene dyes by illustrating the relationships between multiple emission behaviors and the aggregation states of boron-dipyrromethene molecules.
Suggested Citation
Dan Tian & Fen Qi & Huili Ma & Xiaoqing Wang & Yue Pan & Runfeng Chen & Zhen Shen & Zhipeng Liu & Ling Huang & Wei Huang, 2018.
"Domino-like multi-emissions across red and near infrared from solid-state 2-/2,6-aryl substituted BODIPY dyes,"
Nature Communications, Nature, vol. 9(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05040-8
DOI: 10.1038/s41467-018-05040-8
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