Radical pair formation in .gamma.-irradiated 2-methyltetrahydrofuran rigid solutions of polynitrobenzenes

1981 ◽  
Vol 85 (12) ◽  
pp. 1701-1704 ◽  
Author(s):  
S. Konishi ◽  
M. Hoshino ◽  
M. Imamura
Author(s):  
Sergey V. Bondarchuk

This puzzle illustrates how explosive and non-explosive salts can be separated using pressure-dependence of the cationic charges.


2014 ◽  
Vol 79 (3) ◽  
pp. 221-226 ◽  
Author(s):  
G. E. Milanovsky ◽  
V. V. Ptushenko ◽  
D. A. Cherepanov ◽  
A. Yu. Semenov

2021 ◽  
Author(s):  
Hao Su ◽  
Xuepeng Zhang ◽  
Guoqing Zhang

The molecular orbital (MO) theory is an indispensable model to describe the interaction between two molecular species, particularly during chemical bond formation. Here we show that by plotting the energy difference (E<sub>DA</sub>) of the HOMO of an electron donor and the LUMO of an acceptor against their overlap integral (S<sub>DA</sub>), many similar types of bimolecular interactions tend to be clustered near one another on the 2D map. Interestingly, in one of the six arbitrarily divided sections designated as “B2”, the interacting molecular pairs appear to present a type of interaction as a “hybrid” between chemical reaction and radical pair formation, a lesser explored area of research. We propose that such interactions could be crucial for the development of materials with unique optical, magnetic, and catalytic properties from purely organic molecules.<br>


2019 ◽  
Vol 21 (37) ◽  
pp. 20628-20640
Author(s):  
Arghya Pratim Ghosh ◽  
Abdullah Al Mamun ◽  
Pawel M. Kozlowski

The topology of the S1 PES is modulated by introducing a mutation at the F708 position. The mutation influences the photoactivation of the Co–C bond by decreasing the rate of geminate recombination and altering the rate of radical pair formation.


Author(s):  
Michel Geoffroy ◽  
Michel Wermeille ◽  
Paule Castan ◽  
Diane Deguenon ◽  
Gérald Bernardinelli

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