ChemInform Abstract: ELECTRON TRANSFER PROCESSES. PART 28. NUCLEOPHILIC SUBSTITUTION IN ORGANOMERCURY HALIDES BY A FREE-RADICAL CHAIN PROCESS

1982 ◽  
Vol 13 (23) ◽  
Author(s):  
G. A. RUSSEL ◽  
J. HERSHBERGER ◽  
K. OWENS
1988 ◽  
Vol 1 (5) ◽  
pp. 299-303 ◽  
Author(s):  
Glen A. Russell ◽  
Shuisheng Hu ◽  
S. Herron ◽  
Woonphil Baik ◽  
P. Ngoviwatchai ◽  
...  

1990 ◽  
Vol 68 (10) ◽  
pp. 1662-1667 ◽  
Author(s):  
Dennis D. Tanner ◽  
Abdelmajid Kharrat ◽  
H. Oumar-Mahamat

The reduction of p-benzoquinone (BQ) by 1-benzyl-1,4-dihydronicotinamide (BNAH) proceeds by a free-radical chain mechanism initiated by single electron transfer (SET). In dry deoxygenated acetonitrile, the chain, whose propagation steps contain a SET–hydrogen atom transfer sequence, could be inhibited by dinitrobenzene and initiated by di-tert-butylperoxyoxalate. The reduction does not follow second-order reaction kinetics. The fractional order of each reactant was found to be 0.80 and 1.36 for BNAH and BQ, respectively. The AG0 values for both the initiation and the propagation steps were evaluated electro-chemically (CV) and were found to be of a reasonable magnitude to sustain a free-radical chain process. Keywords: 1-benzyl-1,4-dihydronicotinamide, p-benzoquinone, free radical, reduction.


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