ChemInform Abstract: RADICAL IONS OF CONJUGATED POLYCYCLIC HYDROCARBONS CONTAINING TWO PHENALENYL Π-SYSTEMS

1984 ◽  
Vol 15 (40) ◽  
Author(s):  
F. GERSON ◽  
J. KNOEBEL ◽  
A. METZGER ◽  
I. MURATA ◽  
K. NAKASUJI
1984 ◽  
Vol 67 (4) ◽  
pp. 934-938 ◽  
Author(s):  
Fabin Gerson ◽  
Jürgen Knöbel ◽  
André Metzger ◽  
Ichiro Murata ◽  
Kazhior Nakasuji

1993 ◽  
Vol 58 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Rudolf Zahradník

The energies and heats of ion-molecule reactions have been calculated (MP4/6-31G**//6-31G** or better level) and compared with the experimental values obtained from the heats of formation. Two main types of reactions have been studied: (i) AHn + AHn+• ↔ AHn+1+ + AHn-1• (A = C to F and Si to Cl), (ii) AHn + BHm+• ↔ AHn+1+ + BHm-1• or AHn-1+• + BHm+1+ (A and B = C to F). In contrast to (i), processes of type (ii) permit easy differentiation between the proton transfer and hydrogen atom abstraction mechanisms. A third type of interaction involves reactions with radical anions (A = Li to F); comparison was made with analogous processes with radical cations. A brief comment is made about the influence of the level of computational sophistication on the energies and heats of reaction, as well as on the stabilization energy of a hydrogen bonded intermediate, a structure which is similar to that of the reaction products.


2021 ◽  
Author(s):  
Takumi Nakazato ◽  
Haruka Takekoshi ◽  
Takahiro Sakurai ◽  
Hiroshi Shinokubo ◽  
Yoshihiro Miyake

1984 ◽  
Vol 22 (3) ◽  
pp. 321-328 ◽  
Author(s):  
Alan Hewer ◽  
David H. Phillips ◽  
Ruth M. Hodgson ◽  
Philip L. Grover

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