Acidity constants and reactivities of the benzidine and N,N-dimethylbenzidine dications, the two electron oxidation intermediates of benzidine carcinogens

2000 ◽  
Vol 78 (9) ◽  
pp. 1178-1185
Author(s):  
Robert A McClelland ◽  
Daniel Ren ◽  
Raechelle D'Sa ◽  
Abid R Ahmed

This paper describes the behavior in aqueous solutions of the two electron oxidation products of the carcinogens benzidine and N,N-dimethylbenzidine. In biological systems there is evidence that these diamines are oxidized by peroxidases, and that a product of this oxidation may be partly responsible for carcinogenicity. Entry into the oxidation products in the present study was provided through the bis-perchlorate salts of dications obtained upon chemical oxidation and through the irradiation of 4'-amino and 4'-N,N-dimethylamino-4-azidobiphenyls. The benzidine oxidation product exists in three conjugate acid-base forms, a dication, a monocation and neutral bisimine, with pKa(1) = 5.0 and pKa(2) = 9.0. These values stand in marked contrast to ones previously obtained for the two electron oxidation product of p-phenylenediamine, pKa(1) < 1.5 and pKa(2) = 5.75. The dimethylamino derivative, blocked from forming the neutral form, exists as a dication and monocation, with pKa = 5.0. Both systems are quite long-lived in aqueous solution, but they do decay on the minutes-to-hours time scale. The kinetics can be explained by reactions of both the dication and the monocation with water, with a reaction of hydroxide and the monocation becoming important around pH 10. One surprising result is that the monocations are two orders of magnitude more reactive than the dications. Thus, at neutral pH the form that exists in both systems is the monocation, and this is the species that is the most reactive towards the solvent. One of the resonance contributors in the monocation is a 4-biphenylylnitrenium ion. Comparison with other 4'-substituted-4-biphenylylnitrenium ions studied by laser flash photolysis shows that the 4'-amino- and 4'-dimethylamino substituents are highly kinetically stabilizing. These cations, for example, are a billion-fold longer-lived in aqueous solution than the parent 4-biphenylylnitrenium ion.Key words: quinone bisimine, nitrenium, aryl azide.

2011 ◽  
Vol 343-344 ◽  
pp. 469-475
Author(s):  
Wen Yan Shi ◽  
Jian Zhong Gu ◽  
Zheng Jiao ◽  
Wen Jing Wu ◽  
Gang Xu ◽  
...  

(+)-alpha-phenylglycine are significant contaminants at pharmaceutical intermediates production. To study processes for the destruction of contaminant L(+)-alpha-phenylglycine in acid aqueous solution we have investigated the transient species using both laser flash photolysis. The OH· reaction with L(+)-alpha-phenylglycine process was investigated and formed polymer. Furthermore, the results of steady-state analysis suggested that L(+)-alpha-phenylglycine removal was found to be more efficient with increasing applied dose. L(+)-alpha-phenylglycine, decreased by 44.50%, using a dose of 14kGy.


2004 ◽  
Vol 43 (3) ◽  
pp. 505-518 ◽  
Author(s):  
Radoslaw A. Wach ◽  
Hisaaki Kudoh ◽  
Maolin Zhai ◽  
Yusa Muroya ◽  
Yosuke Katsumura

1983 ◽  
Vol 56 (2) ◽  
pp. 389-391 ◽  
Author(s):  
Nobuo Shimo ◽  
Nobuaki Nakashima ◽  
Keitaro Yoshihara

2016 ◽  
Vol 15 (3) ◽  
pp. 431-439 ◽  
Author(s):  
Ivan P. Pozdnyakov ◽  
Wei Ding ◽  
Jing Xu ◽  
Long Chen ◽  
Feng Wu ◽  
...  

An Fe(iii)–As(iii) complex was characterized by UV/Vis spectra and its laser flash photolysis via ligand-to-metal charge transfer resulted in the intermediate of Fe(ii)–As(iv).


2012 ◽  
Vol 28 (04) ◽  
pp. 957-962 ◽  
Author(s):  
YUAN Hai-Xia ◽  
◽  
PAN Hu-Xiang ◽  
WU Yan-Lin ◽  
ZHAO Jian-Feng ◽  
...  

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