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Aggregation-Induced Emission: Effects of Molecular Structure, Solid-State Conformation, and Morphological Packing Arrangement on Light-Emitting Behaviors of Diphenyldibenzofulvene Derivatives

Tong, Hui, Dong, Yongqiang, Hong, Yuning, Häussler, Matthias, Lam, Jacky W. Y., Sung, Herman H.-Y., Yu, Xiaoming, Sun, Jiaxin, Williams, Ian D., Kwok, Hoi Sing, Tang, Ben Zhong·2007·The Journal of Physical Chemistry C

Abstract

Propeller-shaped molecules diphenyldibenzofulvene ( 1 ) and (4-methoxyphenyl)phenyldibenzofulvene ( 2 ) were nonemissive when dissolved in good solvents but became luminescent when aggregated in poor solvents or in the solid state, showing a novel phenomenon of aggregation-induced emission (AIE). 8-Phenylbenzo[ e ]acephenanthrylene ( 3 ), a ring-closed form of 1 with one of its phenyl blades locked, was emissive in the solutions, suggesting that the AIE effects of 1 and 2 are caused by the restrictions of intramolecular rotations of their aromatic blades in the aggregation state. The crystals of 1 and 2 emitted stronger, bluer lights than their amorphous powders, possibly due to the structural rigidification and conformational twisting of the dye molecules in the crystalline phase. The light-emitting diodes with a device configuration of ITO/NPB/dye/BCP/Alq 3 /LiF/Al were fabricated, which emitted bluish-green and yellow lights with maximum luminance and current efficiency up to 5000 Cd/m 2 and 1.90 Cd/A, respectively.

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Authors
Tong, H., Dong, Y., Hong, Y., Häussler, M., Lam, J. W. Y., Sung, H. H.-Y., Yu, X., Sun, J., Williams, I. D., Kwok, H. S., & Tang, B. Z.
Venue
The Journal of Physical Chemistry C
Published
2007-01-18
Volume
111
Issue
5
Pages
2287-2294
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W2035848294
Cited by
281
References
0
FWCI
7.31
Type
journal article
Language
en
Open access
closed

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