The linear tetraphosphine 1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane (tetraphos-1, P4) was used as its rac and meso isomers for the synthesis of both molecularly defined and in situ formed Fe(II) complexes. These were used as precatalysts for sodium bicarbonate hydrogenation to formate and formic acid dehydrogenation to hydrogen and carbon dioxide with moderate to good activities in comparison to those for literature systems based on Fe. Mechanistic details of the reaction pathways were obtained by NMR and HPNMR experiments, highlighting the role of the Fe(II) monohydrido complex [FeH(rac-P4)]+ as a key intermediate. X-ray crystal structures of different complexes bearing rac-P4 were also obtained and are described herein.

Iron(II) Complexes of the Linear rac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation

Bertini Federica;Mellone Irene;Ienco Andrea;Peruzzini Maurizio;Gonsalvi Luca
2015

Abstract

The linear tetraphosphine 1,1,4,7,10,10-hexaphenyl-1,4,7,10-tetraphosphadecane (tetraphos-1, P4) was used as its rac and meso isomers for the synthesis of both molecularly defined and in situ formed Fe(II) complexes. These were used as precatalysts for sodium bicarbonate hydrogenation to formate and formic acid dehydrogenation to hydrogen and carbon dioxide with moderate to good activities in comparison to those for literature systems based on Fe. Mechanistic details of the reaction pathways were obtained by NMR and HPNMR experiments, highlighting the role of the Fe(II) monohydrido complex [FeH(rac-P4)]+ as a key intermediate. X-ray crystal structures of different complexes bearing rac-P4 were also obtained and are described herein.
2015
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
iron phosphine complexes
formic acid dehydrogenation
bicarbonate hydrogenation
X-ray crystallography
HPNMR mechanistic studies
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Descrizione: This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © 2015 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/cs501998t.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/275667
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