Abstract
AbstractThe reaction of the unsymmetrical aliphatic tripodal ligand N[(CH2CH2NH2)(CH2CH2OH)(CH2CH2CH2OH)] (H4‐3) with tris(acetylacetonato)iron(III) gives the dinuclear bis(μ‐alkoxo) bridged complex [Fe{N(CH2CH2N=C(CH3)CHC(CH3)O)‐ (CH2CH2CH2O)(CH2CH2O)}]2 [Fe(η5, μ‐4)]2 (5). The new ligand 43‐ is obtained by reaction of the primary amine function of H4‐3 with one of the acetylacetonato ligands under imine formation. The iron atoms in complex 5 are coordinated in an octahedral fashion within an N2O4 environment. Complex 5 contains three different alkoxo donor groups.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Zeitschrift für anorganische und allgemeine Chemie
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
