Phosphane-Pyridine Iron Complexes: Synthesis, Characterization and Application in Reductive Amination through the Hydrosilylation Reaction

A series of 6 cyclopentadienyl phosphanyl‐pyridine piano‐stool iron complexes was prepared in good yields, characterized, and studied in the catalytic reductive amination of benzaldehyde derivatives through hydrosilylation reactions by using polymethylhydrosiloxane as the hydrosilane source and in d...

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Published in:European journal of inorganic chemistry Vol. 2012; no. 22; pp. 3546 - 3550
Main Authors: Jaafar, Hassen, Li, Haoquan, Misal Castro, Luis C., Zheng, Jianxia, Roisnel, Thierry, Dorcet, Vincent, Sortais, Jean-Baptiste, Darcel, Christophe
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 01-08-2012
WILEY‐VCH Verlag
Wiley-VCH Verlag
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Summary:A series of 6 cyclopentadienyl phosphanyl‐pyridine piano‐stool iron complexes was prepared in good yields, characterized, and studied in the catalytic reductive amination of benzaldehyde derivatives through hydrosilylation reactions by using polymethylhydrosiloxane as the hydrosilane source and in dimethylcarbonate as the solvent at 40 °C. Single‐crystal X‐ray structural analyses were performed for all the complexes. A series of 6 cyclopentadienyl phosphanyl‐pyridine piano‐stool iron complexes was prepared, characterized, and studied in the catalytic reductive amination of benzaldehyde derivatives in dimethylcarbonate through hydrosilylation reactions by using polymethylhydrosiloxane as the hydrosilane source.
Bibliography:Ministère des Affaires Etrangères
Rennes 1 Foundation
ArticleID:EJIC201200550
Université de Rennes 1
ark:/67375/WNG-RG3K9MG6-Z
Centre National de la Recherche Scientifique (CNRS)
Région Bretagne
Rennes Métropole and Ministère de l′Enseignement Supérieur et de la Recherche
istex:257E5257B14E27DF0BD5102CDCA2332E155803C2
Fundación Gran Mariscal de Ayacucho
Axa Research Fund
ISSN:1434-1948
1099-0682
DOI:10.1002/ejic.201200550