Models of vitamin B6 enzymes. 3. Steric and electronic effects in carbon-hydrogen bond breaking reactions of bis(salicylideneglycinato)cobaltate(III) anions

1990 ◽  
Vol 29 (9) ◽  
pp. 1682-1687 ◽  
Author(s):  
James R. Fischer ◽  
Ross J. Fischer ◽  
Edwin H. Abbott
1974 ◽  
Vol 52 (21) ◽  
pp. 3612-3622 ◽  
Author(s):  
Thérèse Di Paolo ◽  
C. Sandorfy

Infrared measurements show that fluorocarbons containing higher halogens are able to open O—H---O, N—H---N, S—H---S, N—H---O=C, type hydrogen bonds. This is probably due to a competitive mechanism of association consisting in the formation of donor–acceptor complexes. It is suggested that the breaking or perturbation of hydrogen bonds by this mechanism is of importance for the explanation of the anesthetic activity of these compounds.


1983 ◽  
Vol 87 (22) ◽  
pp. 4355-4357 ◽  
Author(s):  
T. L. Mathers ◽  
G. Schoffler ◽  
S. P. McGlynn
Keyword(s):  

2014 ◽  
Vol 33 (23) ◽  
pp. 6819-6829 ◽  
Author(s):  
Grégory Nocton ◽  
Corwin H. Booth ◽  
Laurent Maron ◽  
Louis Ricard ◽  
Richard A. Andersen

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