Distance-dependent formation of electronic charge-transfer states in the ground states of anthracene and pyrene covalently linked to a TEMPO free radical

2019 ◽  
Vol 21 (1) ◽  
pp. 77-88 ◽  
Author(s):  
Alok Kumar Tripathi ◽  
Sushma Kundu ◽  
Ranjan Das

Charge-transfer states are shown in molecules consisting of a covalently linked anthracene or pyrene moiety (acceptor) and a TEMPO free radical (donor) through a spacer group of different lengths. Efficiency of the formation of CT states decreases exponentially with the distance separating the two moieties.

2020 ◽  
pp. 2004132
Author(s):  
Marc‐André Rose ◽  
Břetislav Šmíd ◽  
Mykhailo Vorokhta ◽  
Ivetta Slipukhina ◽  
Michael Andrä ◽  
...  

1996 ◽  
Vol 46 (S2) ◽  
pp. 929-930 ◽  
Author(s):  
Andrei N. Timoshevskii ◽  
Vladimir S. Melnikov ◽  
Alexander E. Krasovskii

2020 ◽  
Vol 124 (26) ◽  
pp. 5465-5473
Author(s):  
Marco Franco-Pérez ◽  
José L. Gázquez ◽  
Paul W. Ayers ◽  
Alberto Vela

2010 ◽  
Vol 604 (5-6) ◽  
pp. 548-554 ◽  
Author(s):  
K. Mitsuhara ◽  
Y. Kitsudo ◽  
H. Matsumoto ◽  
A. Visikovskiy ◽  
M. Takizawa ◽  
...  

2000 ◽  
Vol 214 (2) ◽  
Author(s):  
Wolfram Lorenz

Exploration of electronic charge transfer requires quantumtheoretical support. On the line of previous work, the dynamical and quantumchemical foundation of electronic charge density transfer, or partial charge transfer in condensed-matter chemical processes, is explicated in terms of charge density conservation and local completeness of finite LCAO expansion. Accompanying discussion is focussed on recent


2001 ◽  
Vol 489 (1-3) ◽  
pp. L561-L567 ◽  
Author(s):  
I. Vaquila ◽  
J.W. Rabalais ◽  
J. Wolfgang ◽  
P. Nordlander

Sign in / Sign up

Export Citation Format

Share Document