Literature DB >> 26480334

A Low-Valent Iron Imido Heterocubane Cluster: Reversible Electron Transfer and Catalysis of Selective C-C Couplings.

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 CC couplings and even allow catalytic one-pot reactions, which show a remarkably enhanced selectivity in the presence of the [Fe4 N4 ] heterocubanes.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Keywords:  CC coupling; cluster compounds; heterocubanes; homogeneous catalysis; low-valent iron

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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


  1 in total

1.  Efficient Dehydration of C6-10-α,ω-Alkanediols to Alkadienes as Catalyzed by Aliphatic Acids.

Authors:  Chongzhi Mao; Shaodong Zhou; Chao Qian; Jiancheng Ruan; Xinzhi Chen
Journal:  ACS Omega       Date:  2019-10-08
  1 in total

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