期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 14, 页码 7851-7859出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202015390
关键词
BODIPY; fluorescence; organic dye; self-assembly; supramolecular polymer
资金
- DST-SERB, Govt. of India [SB/S2/JCB-11/2014]
- CSIR
- UGC, Govt. of India
In this study, the creation and control of distinct supramolecular energy landscapes for reversible control of excited-state emission processes were demonstrated through cascade energy transfer in chromophore assemblies. Enhanced near-infrared emission was achieved by manipulating morphology and excitation energy transfer with variable solvent composition and ultrasound stimulation.
Excited state properties such as emission, exciton transport, electron transfer, etc., are strongly dependent on the shape, size and molecular arrangement of chromophore based supramolecular architectures. Herein, we demonstrate creation and control of distinct supramolecular energy landscapes for the reversible control of the excited-state emission processes through cascade energy transfer in chromophore assemblies, facilitated by an unprecedented solvent effect. In methylcyclohexane, a tailor-made Y-shaped BODIPY derivative self-assembles to form an unusual spherical architecture of 400-1200 nm size, which exhibits a single emission at 540 nm upon 475 nm excitation through a normal excitation deactivation process. However, in n-decane, the same BODIPY derivative forms two-dimensional supramolecular sheets, exhibiting multiple emission peaks at 540, 610, 650, 725 and 790 nm with 475 nm excitation due to cascade energy transfer. Further control on the morphology and excitation energy transfer is possible with variable solvent composition and ultrasound stimulation, resulting in enhanced near-infrared emission with an overall pseudo Stokes shift of 7105 cm(-1).
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