| Literature DB >> 26480334 |
Crispin Lichtenberg1, Inés Garcia Rubio1,2, Liliana Viciu1, Mario Adelhardt3, Karsten Meyer3, Gunnar Jeschke1, Hansjörg Grützmacher4.
Abstract
Enzymes and cofactors with iron-sulfur heterocubane core structures, [Fe4 S4 ], are often found in nature as electron transfer reagents in fundamental catalytic transformations. An artificial heterocubane with a [Fe4 N4 ] core is reported that can reversibly store up to four electrons at very negative potentials. The neutral [Fe4 N4 ] and the singly reduced low-valent [Fe4 N4 ](-) heterocubanes were isolated and fully characterized. The low-valent species bears one unpaired electron, which is localized predominantly at one iron center in the electronic ground state but fluctuates with increasing temperatures. The electrons stored or released by the [Fe4 N4 ]/[Fe4 N4 ](-) redox couple can be used in reductive or oxidative CC couplings and even allow catalytic one-pot reactions, which show a remarkably enhanced selectivity in the presence of the [Fe4 N4 ] heterocubanes.Entities:
Keywords: CC coupling; cluster compounds; heterocubanes; homogeneous catalysis; low-valent iron
Mesh:
Substances:
Year: 2015 PMID: 26480334 DOI: 10.1002/anie.201505668
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336