Organized Aggregation Makes Insoluble Perylene Diimide Efficient for the Reduction of Aryl Halides via Consecutive Visible Light-Induced Electron-Transfer Processes

2016 ◽  
Vol 138 (12) ◽  
pp. 3958-3961 ◽  
Author(s):  
Le Zeng ◽  
Tao Liu ◽  
Cheng He ◽  
Dongying Shi ◽  
Feili Zhang ◽  
...  
ChemInform ◽  
2015 ◽  
Vol 46 (19) ◽  
pp. no-no
Author(s):  
Indrajit Ghosh ◽  
Tamal Ghosh ◽  
Javier I. Bardagi ◽  
Burkhard Koenig

Science ◽  
2014 ◽  
Vol 346 (6210) ◽  
pp. 725-728 ◽  
Author(s):  
I. Ghosh ◽  
T. Ghosh ◽  
J. I. Bardagi ◽  
B. Konig

2016 ◽  
Vol 18 (11) ◽  
pp. 7875-7887 ◽  
Author(s):  
K. J. Lee ◽  
J. H. Woo ◽  
E. Kim ◽  
Y. Xiao ◽  
X. Su ◽  
...  

The photophysical properties of novel donor–acceptor dyad and triad molecules show an intricate interplay between energy and electron transfer processes.


2022 ◽  
Author(s):  
Pooja Rana ◽  
Bhawna Kaushik ◽  
Rashmi Gaur ◽  
Sriparna Dutta ◽  
Sneha Yadav ◽  
...  

In this work, we have reported a noble metal free heterogeneous photocatalyst to carry out direct (Het)Arene C-H arylation and solvent-free CO2 capture via single-electron transfer processes at room temperature...


Nanoscale ◽  
2018 ◽  
Vol 10 (23) ◽  
pp. 10934-10944 ◽  
Author(s):  
Anna Isakova ◽  
Safakath Karuthedath ◽  
Thomas Arnold ◽  
Jonathan R. Howse ◽  
Paul D. Topham ◽  
...  

Symmetry-breaking charge transfer in donor–acceptor blends comprising perylene diimide avoids strongly-bound interfacial states and outperforms excimer formation.


2021 ◽  
Author(s):  
Eloïse Colson ◽  
Julie Andrez ◽  
Ali Dabbous ◽  
Frabrice Dénès ◽  
Vincent Maurel ◽  
...  

A mild and simple protocol for the synthesis of 8-azabicyclo[3.2.1]octane and 9-azabicyclo[3.3.1]nonane derivatives is described. It provides these valuable bicyclic alkaloid skeletons in good yields and high levels of diastereoselectivity from simple and readily available starting materials using visible-light photoredox catalysis. This unprecedented annulation process takes advantage of the unique reactivity of ethyl 2-(acetoxymethyl)acrylate as a 1,3-bis radical acceptor and of cyclic N,N-dialkylanilines as radical 1,3-bis radical donors. The success of this process relies on efficient electron transfer processes and highly selective deprotonation of aminium radical cations leading to the key α-amino radical intermediates.


2021 ◽  
Author(s):  
Eloïse Colson ◽  
Julie Andrez ◽  
Ali Dabbous ◽  
Frabrice Dénès ◽  
Vincent Maurel ◽  
...  

A mild and simple protocol for the synthesis of 8-azabicyclo[3.2.1]octane and 9-azabicyclo[3.3.1]nonane derivatives is described. It provides these valuable bicyclic alkaloid skeletons in good yields and high levels of diastereoselectivity from simple and readily available starting materials using visible-light photoredox catalysis. This unprecedented annulation process takes advantage of the unique reactivity of ethyl 2-(acetoxymethyl)acrylate as a 1,3-bis radical acceptor and of cyclic N,N-dialkylanilines as radical 1,3-bis radical donors. The success of this process relies on efficient electron transfer processes and highly selective deprotonation of aminium radical cations leading to the key α-amino radical intermediates.


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