Low-Valent α-Diimine Iron Complexes for Catalytic Olefin Hydrogenation

2005 ◽  
Vol 24 (23) ◽  
pp. 5518-5527 ◽  
Author(s):  
Suzanne C. Bart ◽  
Eric J. Hawrelak ◽  
Emil Lobkovsky ◽  
Paul J. Chirik
2012 ◽  
Vol 51 (12) ◽  
pp. 6719-6730 ◽  
Author(s):  
Eva-Maria Schnöckelborg ◽  
Marat M. Khusniyarov ◽  
Bas de Bruin ◽  
František Hartl ◽  
Thorsten Langer ◽  
...  

2014 ◽  
Vol 20 (16) ◽  
pp. 4754-4761 ◽  
Author(s):  
Elise Salanouve ◽  
Ghania Bouzemame ◽  
Sébastien Blanchard ◽  
Etienne Derat ◽  
Marine Desage-El Murr ◽  
...  
Keyword(s):  

2008 ◽  
Vol 130 (6) ◽  
pp. 1992-2004 ◽  
Author(s):  
Alois Fürstner ◽  
Keisuke Majima ◽  
Rubén Martín ◽  
Helga Krause ◽  
Egmont Kattnig ◽  
...  

2014 ◽  
Vol 67 (7) ◽  
pp. 1011 ◽  
Author(s):  
Lea Fohlmeister ◽  
Cameron Jones

A toluene-capped guanidinato iron(i) complex [(Pipiso)Fe(η6-toluene)] (Pipiso = [(DipN)2C(cis-NC5H8Me2-2,6)]–) was prepared by magnesium metal reduction of {[(Pipiso)FeII(µ-Br)]2} in toluene. The reactivity of the closely related FeI–FeI multiply bonded species, {[Fe(μ-Pipiso)]2} towards a range of unsaturated small molecule substrates was investigated, and found to be broadly similar to that of low-valent β-diketiminato iron complexes. That is, its reaction with CO yielded the iron(i) carbonyl complex [(Pipiso)Fe(CO)3], whereas reaction with CO2 formed the same product via an apparent reductive disproportionation of the substrate. In contrast, reaction between {[Fe(μ-Pipiso)]2} and CS2 led to reductive C=S bond cleavage and the isolation of {[(Pipiso)Fe]2(μ-S)(μ-CS)}. Different reactivity was seen with AdN3 (Ad = 1-adamantyl), which was reductively coupled by the iron(i) dimer to give iron(ii) hexaazenyl complex {[(Pipiso)Fe]2(μ-AdN6Ad)}.


ChemInform ◽  
2008 ◽  
Vol 39 (27) ◽  
Author(s):  
Alois Fuerstner ◽  
Keisuke Majima ◽  
Ruben Martin ◽  
Helga Krause ◽  
Egmont Kattnig ◽  
...  

ChemInform ◽  
2014 ◽  
Vol 45 (45) ◽  
pp. no-no
Author(s):  
Elise Salanouve ◽  
Ghania Bouzemame ◽  
Sebastien Blanchard ◽  
Etienne Derat ◽  
Marine Desage-El Murr ◽  
...  
Keyword(s):  

2020 ◽  
Vol 65 (6) ◽  
pp. 1142-1153
Author(s):  
В.Д. Микоян ◽  
◽  
Е.Н. Бургова ◽  
Р.Р. Бородулин ◽  
А.Ф. Ванин ◽  
...  

The number of mononitrosyl iron complexes with diethyldithiocarbamate, formed in the liver of mice in vivo and in vitro after intraperitoneal injection of binuclear dinitrosyl iron complexes with N-acetyl-L-cysteine or glutathione, S-nitrosoglutathione, sodium nitrite or the vasodilating drug Isoket® was assessed by electron paramagnetic resonance (EPR). The number of the said complexes, in contrast to the complexes, formed after nitrite or Isoket administration, the level of which sharply increased after treatment of liver preparations with a strong reducing agent - dithionite, did not change in the presence of dithionite. It was concluded that, in the first case, EPR-detectable mononitrosyl iron complexes with diethyldithiocarbamate in the absence and presence of dithionite appeared as a result of the reaction of NO formed from nitrite with Fe2+-dieth- yldithiocarbamate and Fe3+-diethyldithiocarbamate complexes, respectively. In the second case, mononitrosyl iron complexes with diethyldithiocarbamate appeared as a result of the transition of iron-mononitosyl fragments from ready-made iron-dinitrosyl groups of binuclear dinitrosyl complexes, which is three to four times higher than the content of the mononuclear form of these complexes in the tissue...


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