Identification of the EPR-Active Iron-Nitrosyl Complexes in Mammalian Ferritins

Biochemistry ◽  
1994 ◽  
Vol 33 (12) ◽  
pp. 3679-3687 ◽  
Author(s):  
Minghe Lee ◽  
Paolo Arosio ◽  
Anna Cozzi ◽  
N. Dennis Chasteen

2007 ◽  
pp. 3562 ◽  
Author(s):  
Sandra A. T. Dillinger ◽  
Helmut W. Schmalle ◽  
Thomas Fox ◽  
Heinz Berke




ACS Catalysis ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 10499-10518 ◽  
Author(s):  
Nicolai Lehnert ◽  
Kiyoshi Fujisawa ◽  
Stephanie Camarena ◽  
Hai T. Dong ◽  
Corey J. White


2016 ◽  
Vol 128 (47) ◽  
pp. 14795-14799 ◽  
Author(s):  
Pauline N. Serrano ◽  
Hongxin Wang ◽  
Jason C. Crack ◽  
Christopher Prior ◽  
Matthew I. Hutchings ◽  
...  






2007 ◽  
Vol 414 (1) ◽  
pp. 102-105 ◽  
Author(s):  
S. V. Vasil’eva ◽  
A. N. Osipov ◽  
N. A. Sanina ◽  
S. M. Aldoshin


1973 ◽  
Vol 28 (5-6) ◽  
pp. 300-305 ◽  
Author(s):  
G. Martini ◽  
E. Tiezzi

ESR has been used in the study of iron(I)-nitrosyl complexes with organic ligands in solution. Four types of complexes have been identified on basis of the ESR parameters, namely Fe (NO) L5, Fe (NO) L2, Fe (NO) 2L2, and Fe (NO) 2L. In the iron-nitrosyl complexes with the organic ligands used, the groups more often involved in the coordination are: - C -NH2; - C -NH; -C= O; and - C = S (eventually in the tautomeric forms). Urea and derivatives, either in water or in ethanol solutions, seem to give rise only to Fe (NO)2L2 type complexes. Similar results were obtained with phenylamino-derivatives and heterocycles. Equilibria between different types of complexes - Fe (NO) L2 and Fe (NO) 2L - were established with hydrazides and substituted hydrazides.



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