Importance of Substituent Intramolecular Charge-Transfer Effect on the Molecular Conformation of Diphenyl Ethers

1998 ◽  
Vol 63 (26) ◽  
pp. 9794-9800 ◽  
Author(s):  
Bunji Uno ◽  
Takuya Iwamoto ◽  
Noriko Okumura
Nanoscale ◽  
2020 ◽  
Vol 12 (32) ◽  
pp. 16685-16689
Author(s):  
Sojeong Heo ◽  
Ka Young Kim ◽  
Heekyoung Choi ◽  
Seok Gyu Kang ◽  
Wonjin Choi ◽  
...  

The strong exciplex emission of the supramolecular polymer I with yellow emission was a consequence of the intramolecular charge transfer interactions in a mixed DMSO/H2O (60 : 40–1 : 99 v/v) solution.


2020 ◽  
Author(s):  
Hojeong Park ◽  
Shijie Li ◽  
Guangle Niu ◽  
Haoke Zhang ◽  
Zhuoyue Song ◽  
...  

Fatty liver disease (FLD) has become an increasing global health risk. However, an accurate diagnosis of FLD at an early stage remains a great challenge due to lack of suitable imaging tools. To this end, we developed the first fluorescent two-photon aggregationinduced emission (AIE) luminogen ABCXF for high-contrast imaging of FLD tissue. ABCXF has a large Stokes shift, good two-photon absorption cross-section, bright red emission, high fluorescence quantum yield in solid state, and excellent photostability. It shows abnormal intramolecular charge transfer effect instead of twisted intramolecular charge transfer effect in polar solvents. Photophysical and crystal data demonstrated that it exhibits nonaromatic rotors - trifluoromethyto contribute to its AIE effect. Biocompatible lipid droplet-targeting ABCXF can selectively light up lesions in the FLD tissue with a high signal-to-noise ratio. It shows superior imaging performances compared to Oil Red O. Thus, ABCXF can be a powerful tool for the diagnosis and evaluation of FLD from a liver biopsy.


2018 ◽  
Vol 54 (3) ◽  
pp. 303-306 ◽  
Author(s):  
Junhui Miao ◽  
Bin Meng ◽  
Jun Liu ◽  
Lixiang Wang

The use of an A–D–A′–D–A strategy to develop small molecule acceptors with broad absorption spectra through suppressing the intramolecular charge transfer effect is studied.


2014 ◽  
Vol 1033-1034 ◽  
pp. 1109-1113
Author(s):  
Ting Feng Tan ◽  
Bian Peng Wu ◽  
Li Gang Bai ◽  
Yan Xia Li ◽  
Ming Jie Zhang

Asymmetric 2-p-nitrophenyl-5-naphthylmethylene-1,3,4-oxadiazole and 2-p-aminophenyl-5-naphthylmethylene-1,3,4-oxadiazole were synthesized and characterized by IR、1HNMR and MS analysis, and their optical properties were detected using UV-vis absorption spectroscopy and fluorescence spectroscopy. The existence of electron-withdrawing oxadiazole units causes a significant bathochromic shift of the UV absorption maximum. The largest UV-absorption peak of target compounds is in the range of 298-317 nm, and a new emission band at 402 nm is formed. The fluorescence intensity is gradually enhanced, which strengthens the intramolecular charge transfer effect between the electron-withdrawing oxadiazole and electron-donating aniline.


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