NIR electrochemical fluorescence switching from polymethine dyes

2014 ◽  
Vol 5 (4) ◽  
pp. 1538-1544 ◽  
Author(s):  
Seogjae Seo ◽  
Simon Pascal ◽  
Chihyun Park ◽  
Kyoungsoon Shin ◽  
Xu Yang ◽  
...  

Reversible electrochemical fluorescence switching in the NIR region is achieved by the reversible redox reaction of an NIR emissive polymethine dye.

2018 ◽  
Vol 256 ◽  
pp. 107-116 ◽  
Author(s):  
Ping Chen ◽  
Aiwu Zhao ◽  
Jin Wang ◽  
Qinye He ◽  
Henghui Sun ◽  
...  

Author(s):  
Manlin Fu ◽  
Kai Wang ◽  
Qiancheng Ma ◽  
Mianli Bian ◽  
Qing Zhu

Abnormal changes in intracellular viscosity and cysteine are both associated with several important biological processes such as reversible redox reaction, which plays a pivotal role in the process of inflammation....


2018 ◽  
Vol 9 (23) ◽  
pp. 5178-5182 ◽  
Author(s):  
Xiaodan Huang ◽  
Yang Liu ◽  
Chao Liu ◽  
Jun Zhang ◽  
Owen Noonan ◽  
...  

An aluminum–selenium battery powered by the reversible redox reaction of Se/Se2Cl2 has been developed for the first time.


1990 ◽  
Vol 10 (3) ◽  
pp. 139-145 ◽  
Author(s):  
K. -H. Feller ◽  
R. Gadonas ◽  
V. Krasauskas

Results are presented of time-resolved absorption investigations of energy transfer processes between a polymethine dye and an iron complex dye (dye E). For the first time the acceptor molecule transient absorption depletion generated by energy transfer from an excited donor was observed. The decay time of the acceptor deactivation (≈ 140 Ps) in the presence of the energy donor agrees very well with the S1-state lifetime of the energy donor.


2016 ◽  
Vol 4 (42) ◽  
pp. 16312-16317 ◽  
Author(s):  
Abdul Muqsit Khattak ◽  
Zahid Ali Ghazi ◽  
Bin Liang ◽  
Niaz Ali Khan ◽  
Azhar Iqbal ◽  
...  

A redox active pyridine based covalent organic framework was synthesized and used as an electrode in faradaic supercapacitors. The pyridine units in the DAP-COF undergo a reversible redox reaction, leading to an increase in specific capacitance relative to both its electroactive monomer and a COF lacking redox-active groups.


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