Topology of the Effectively Paired and Unpaired Electron Densities for Complex Bonding Patterns: The Three-Center Two-Electron Bonding Case

2009 ◽  
Vol 5 (8) ◽  
pp. 2030-2043 ◽  
Author(s):  
Rosana M. Lobayan ◽  
Roberto C. Bochicchio ◽  
Alicia Torre ◽  
Luis Lain

1963 ◽  
Vol 16 (3) ◽  
pp. 174-177 ◽  
Author(s):  
S. J. Pickart


1966 ◽  
Vol 143 (2) ◽  
pp. 365-372 ◽  
Author(s):  
F. Menzinger ◽  
A. Paoletti


2003 ◽  
Vol 107 (1) ◽  
pp. 127-130 ◽  
Author(s):  
Alicia Torre ◽  
Luis Lain ◽  
Roberto Bochicchio




2017 ◽  
Vol 19 (29) ◽  
pp. 19225-19233 ◽  
Author(s):  
Max Pinheiro ◽  
Luiz F. A. Ferrão ◽  
Fernanda Bettanin ◽  
Adélia J. A. Aquino ◽  
Francisco B. C. Machado ◽  
...  

Strong modulation of the biradical character of acenes with dopant positions is demonstrated by tracking the unpaired electron densities.



1979 ◽  
Vol 40 (C7) ◽  
pp. C7-81-C7-82
Author(s):  
C. Fleurier ◽  
G. Coulaud ◽  
J. Chapelle


1979 ◽  
Vol 44 (6) ◽  
pp. 1731-1741 ◽  
Author(s):  
Andrej Staško ◽  
Ľubomír Malík ◽  
Alexander Tkáč ◽  
Vladimír Adamčík ◽  
Eva Maťašová

Reactions of R2,R3-alkyl substituted 2-hydroxybenzenecarboxylic acids 2-HO-C6H2R2-COOH with Grignard reagents R1MgBr in the presence of nickel give stable aryl alkyl ketyl radicals 2-O--R2-, R3-C6H2-CO--R1 where R1 = CH3, C2H5, C2D5, n-C3H7 and R2,R3 = CH3, C2H5, i-C3H7, t-C4H9. The β protons of ketyl group are equivalent (splitting constant 1.25 mT) and non-equivalent (splitting constants within 0.5 to 1.5 mT) for R1 = methyl and other alkyl groups, respectively. Interaction of the γ protons with the unpaired electron was only observed in the case of R1 = n-propyl (splitting constants about 0.07 mT). The substituents R1 have but slight effect on values of splitting constants of the protons in R2,R3 and vice versa. Also splitting constants of the benzene nucleus (a4H = 0.55 mT, a6H = 0.44 mT) are only slightly affected by the substituents R1,R2,R3, which indicates dominant electron-donor effect of the oxido-anion group eliminating the relatively smaller contributions of the alkyl substituents.



Sign in / Sign up

Export Citation Format

Share Document