Regulation of aggregation-induced emission color of α-cyanostilbene luminogens through donor engineering of amino derivatives

2021 ◽  
Vol 69 ◽  
pp. 152972
Author(s):  
Murat Tonga
2021 ◽  
pp. 109439
Author(s):  
Hui-Ting Mao ◽  
Yang Yang ◽  
Kai-Yue Zhao ◽  
Ying-Chen Duan ◽  
Wei-Lin Song ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (28) ◽  
pp. 23335-23339 ◽  
Author(s):  
Xuefeng Wang ◽  
Lichao Xu ◽  
Dan Mu ◽  
Hua Wang ◽  
Shengyu Feng

Polyphenyl compounds could not emit strong fluorescence and adjust the emission colors. The “silicon effect” appeared to resolve this problem.


2019 ◽  
Vol 20 (8) ◽  
pp. 1891 ◽  
Author(s):  
Jianxing Wang ◽  
Xiangfang Lin ◽  
Tong Shu ◽  
Lei Su ◽  
Feng Liang ◽  
...  

Aggregation-induced emission (AIE) is an intriguing strategy to enhance the luminescence of metal nanoclusters (NCs). However, the morphologies of aggregated NCs are often irregular and inhomogeneous, leading to instability and poor color purity of the aggregations, which greatly limit their further potential in optical applications. Inspired by self-assembly techniques, manipulating metal NCs into well-defined architectures has achieved success. The self-assembled metal NCs often exhibit enhancing emission stability and intensity compared to the individually or randomly aggregated ones. Meanwhile, the emission color of metal NCs becomes tunable. In this review, we summarize the synthetic strategies involved in self-assembly of metal NCs for the first time. For each synthetic strategy, we describe the self-assembly mechanisms involved and the dependence of optical properties on the self-assembly. Finally, we outline the current challenges to and perspectives on the development of this area.


2017 ◽  
Vol 8 (1) ◽  
pp. 577-582 ◽  
Author(s):  
Jing Nan Zhang ◽  
Hui Kang ◽  
Nan Li ◽  
Shi Ming Zhou ◽  
Hua Ming Sun ◽  
...  

Organic solid fluorophores based on p-bis(2,2-dicyanovinyl)benzene were designed and synthesized, which displayed a tunable emission color and substituent dependent optical behavior.


2020 ◽  
Author(s):  
Wooseok Ki ◽  
Kathleen Ngo ◽  
Boris Averkiev ◽  
Phalguni Ghosh ◽  
GorDan T. Reeves ◽  
...  

2019 ◽  
Vol 19 (13) ◽  
pp. 1093-1110 ◽  
Author(s):  
Adel A.H. Abdel Rahman ◽  
Ibrahim F. Nassar ◽  
Amira K.F. Shaban ◽  
Dina S. EL-Kady ◽  
Hanem M. Awad ◽  
...  

Background & Objective:New diaryl-substituted pyrimidinedione compounds, their thioxo derivatives as well as their bicyclic thiazole compounds were synthesized and characterized.Methods:The glycosylamino derivatives of the synthesized disubstituted derivatives of the pyrimidine scaffold were also prepared via reaction of the N3-amino derivatives with a number of monosaccharides followed by acetylation.Results:The anticancer activity of the synthesized compounds was studied against human liver cancer (HepG2) and RPE-1cell lines. Compounds 2a, 2b, 3a and 12 showed potent activities with IC50 results comparable to that of doxorubicin.Conclusion:Docking investigations into Cyclin-dependent kinase 2 (CDK-2) enzyme, a potential target for cancer medication, were also reported showing the possible binding interaction into the enzyme active site to support their activity behavior.


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