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Title

Unsymmetrical cyrhetrenyl and ferrocenyl azines derived from 5-nitrofurane: Synthesis, structural characterization and electrochemistry

AuthorsGómez, Johana; Klahn, A. Hugo; Fuentealba, Mauricio; Sierra, Diego; Olea-Azar, Claudio; Medina, Manuela E. CSIC
KeywordsNitrofurane
Ferrocenyl azines
NMR
Cyclic voltammetry
Crystal structure
Cyrhetrenyl azines
Issue DateNov-2015
PublisherElsevier
CitationInorganic Chemistry Communication 61: 204-206 (2015)
AbstractA new series of unsymmetrical cyrhetrenyl and ferrocenyl azines that were monosubstituted [(η5-C5H4)-C(R)=N-N=CH(5-NO2-2-C4H2O)]M {with M=Re(CO)3 and R=H (1a) or R=Me (1b); M=Fe(η5-C5H5) and R=H (2a) or R=Me (2b)} and disubstituted [Fe{(η5-C5H4)-C(Me)=N-N=CH(5-NO2-2-C4H2O)}2] (3a) were prepared by condensation reactions of the corresponding organometallic hydrazone [(η5-C5H4)-C(R)=N-NH2)]M with 5-nitro-2-furaldehyde. The 1H and 13C{1H} NMR spectra indicated that these compounds adopted an (E,E)-configuration about the 〉C=N - bond and an s-trans conformation about the N1-N2 bond, and this result was confirmed by X-ray crystallographic analyses of 1a and 2b. The opposite electronic effects of the organometallic fragments correlate with the co-planarity of the [(η5-C5H4)-C(R)=N-N=CH(5-NO2-2-C4H2O)] system, the reduction potential of the nitro group (E1/2) and the chemical shifts of the iminic carbons.
Publisher version (URL)https://doi.org/10.1016/j.inoche.2015.10.007
URIhttp://hdl.handle.net/10261/184059
DOIhttp://dx.doi.org/10.1016/j.inoche.2015.10.007
Identifiersdoi: 10.1016/j.inoche.2015.10.007
issn: 1387-7003
Appears in Collections:(ICMM) Artículos
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