scholarly journals Chromophore-radical excited state antiferromagnetic exchange controls the sign of photoinduced ground state spin polarization

2021 ◽  
Author(s):  
Martin L. Kirk ◽  
David A. Shultz ◽  
Patrick Hewitt ◽  
Daniel E. Stasiw ◽  
Ju Chen ◽  
...  

A change in the sign of the ground state electron spin polarization (ESP) is reported in complexes where an organic radical (nitronylnitroxide, NN) is covalently attached to a donor–acceptor chromophore via two different meta-phenylene bridges.

2005 ◽  
Vol 72 (2) ◽  
Author(s):  
S. M. Fischer ◽  
T. Anderson ◽  
P. Kerns ◽  
G. Mesoloras ◽  
D. Svelnys ◽  
...  

2009 ◽  
Vol 48 (12) ◽  
pp. 5049-5051 ◽  
Author(s):  
Eleni E. Moushi ◽  
Theocharis C. Stamatatos ◽  
Wolfgang Wernsdorfer ◽  
Vassilios Nastopoulos ◽  
George Christou ◽  
...  

1957 ◽  
Vol 18 (6) ◽  
pp. 661-662 ◽  
Author(s):  
Sadaaki Yanagawa

1979 ◽  
Vol 40 (1) ◽  
pp. 1-3 ◽  
Author(s):  
E. Warde ◽  
R. Seltz ◽  
G. Costa ◽  
D. Magnac ◽  
C. Gerardin

Author(s):  
N. J. Stone ◽  
C. J. Ashworth ◽  
I. S. Grant ◽  
A. G. Griffiths ◽  
S. Ohya ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (23) ◽  
pp. 4361
Author(s):  
Bogdan Dereka ◽  
Ina Fureraj ◽  
Arnulf Rosspeintner ◽  
Eric Vauthey

The formation of a halogen-bond (XB) complex in the excited state was recently reported with a quadrupolar acceptor–donor–acceptor dye in two iodine-based liquids (J. Phys. Chem. Lett. 2017, 8, 3927–3932). The ultrafast decay of this excited complex to the ground state was ascribed to an electron transfer quenching by the XB donors. We examined the mechanism of this process by investigating the quenching dynamics of the dye in the S1 state using the same two iodo-compounds diluted in inert solvents. The results were compared with those obtained with a non-halogenated electron acceptor, fumaronitrile. Whereas quenching by fumaronitrile was found to be diffusion controlled, that by the two XB compounds is slower, despite a larger driving force for electron transfer. A Smoluchowski–Collins–Kimball analysis of the excited-state population decays reveals that both the intrinsic quenching rate constant and the quenching radius are significantly smaller with the XB compounds. These results point to much stronger orientational constraint for quenching with the XB compounds, indicating that electron transfer occurs upon formation of the halogen bond.


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