Mechanoluminescence and aggregation-enhanced emission (AEE) of an In-MOF based on 9,9’-diphenyl-9H-fluorene tetraacid linker

Nanoscale ◽  
2021 ◽  
Author(s):  
Swati Jindal ◽  
Gulshan Anjum ◽  
Vijay Kumar Maka ◽  
J. Narasimha Moorthy

A water-stable In-MOF, constructed based on a conformationally-flexible tetraacid linker, i.e., 2,7-bis(3,5-dicarboxyphenyl)-9,9’-diphenyl-9H-fluorene, i.e., H4DPF, is shown to exhibit significantly enhanced solid-state fluorescence quantum yield (Φf) of 23% in comparison to...

2006 ◽  
Vol 128 (51) ◽  
pp. 16532-16539 ◽  
Author(s):  
Renqiang Yang ◽  
Andres Garcia ◽  
Dmitry Korystov ◽  
Alexander Mikhailovsky ◽  
Guillermo C. Bazan ◽  
...  

2020 ◽  
Vol 02 (01) ◽  
pp. 033-040 ◽  
Author(s):  
Hua Li ◽  
Haiyang Shu ◽  
Xin Wang ◽  
Xiaofu Wu ◽  
Hongkun Tian ◽  
...  

Halogen bonding, as a kind of intermolecular interaction, has rarely been used to tune solid-state emission properties of luminescent materials, especially fluorescent materials. Herein, three trans-enaminone (TE) derivatives (nonbrominated TE, monobrominated BrTE, and tribrominated Br3TE) with aggregation-induced emission property have been designed and synthesized. Two types of BrTE crystals (BrTE-B and BrTE-G) with different fluorescence properties were obtained. It was observed that their solid-state fluorescence has been enhanced by the formation of halogen bonding. In particular, the crystal BrTE-G containing Br…π interactions exhibits a fluorescence quantum yield (9.6%) nearly sevenfold higher than BrTE-B, the crystal without halogen bonding (1.4%), and fivefold higher than the nonbrominated TE derivative (2.1%). By careful inspection of the single-crystal data and theoretical calculations, the high fluorescence quantum yield of BrTE-G appears to be due to halogen-bonding interactions as well as multiple stronger intermolecular interactions which may restrain molecular motions, leading to the reduced nonradiative decay rate and the enhanced radiative decay rate. Additionally, increasing the number of bromine substituents may further promote the radiative decay rate, explaining therefore the higher fluorescence quantum yield (12.5%) of Br3TE.


2021 ◽  
Author(s):  
Hai-Jiao Wang ◽  
Wan-Yi Hou ◽  
Jing Kang ◽  
Xin-Yu Zhai ◽  
Hongli Chen ◽  
...  

Due to the direct π - π interaction and excessive energy resonance transfer, it is very challenging to prepare CDs with high fluorescence quantum yield (QY) in solid state. In...


Author(s):  
Huey Chong Kwong ◽  
Ai Jia Sim ◽  
C. S. Chidan Kumar ◽  
Ching Kheng Quah ◽  
Suchada Chantrapromma ◽  
...  

In the bischalcone molecule of the title compound, C24H18O4·2C3H7NO, the central benzene and terminal hydroxyphenyl rings form a dihedral angle of 14.28 (11)° and the central C=C double bond adopts a trans configuration. In the crystal, the bischalcone and solvate molecules are interconnected via O—H...O hydrogen bonds, which were investigated by Hirshfeld surface analysis. Solid-state fluorescence was measured at λex = 4400 Å. The emission wavelength appeared at 5510 Å, which corresponds to yellow light and the solid-state fluorescence quantum yield (F f) is 0.18.


Author(s):  
Barbara Panunzi ◽  
Rosita Diana ◽  
Simona Concilio ◽  
Lucia Sessa ◽  
Rafi Shikler ◽  
...  

A highly efficient deep red (DR) emitting organic solid based on a dicyano-phenylenevinylene derivative was reported. The structural and spectroscopic properties of the solid have been described in terms of crystallographic data and time dependent DFT analysis. A noteworthy fluorescence quantum yield of 53% was observed for the brightest emitter cast into solid films. This result can be explained in terms of aggregation-induced emission (AIE) effect.


2019 ◽  
Vol 717 ◽  
pp. 119-123
Author(s):  
Mingcai Xie ◽  
Daocheng Hong ◽  
Sushu Wan ◽  
Mingyi Xie ◽  
Yuxi Tian

RSC Advances ◽  
2018 ◽  
Vol 8 (27) ◽  
pp. 15173-15180 ◽  
Author(s):  
Zhao-Ming Zhang ◽  
Bao-Xi Miao ◽  
Xin-Xue Tang ◽  
Zhong-Hai Ni

Tetraarylethenes with different π-conjugation degrees can be realized by controlling the number of 4,5,9,10-tetrahydropyrene segments. However, the fluorescence quantum yield of these compounds in films doesn't increase with the π-conjugation degree.


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