Organodiiron(II)-complexes containing a long conjugated hydrazonato spacer. Synthesis, charcterization, electrochemical and structural studies

Carolina Manzur, Mauricio Fuentealba, Lorena Millán, Francisco Gajardo, Maria Teresa Garland, Ricardo Baggio, Jose A. Mata, Jean René Hamon, David Carrillo

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

13 Citas (Scopus)

Resumen

Organometallic hydrazines of general formula Me, (2)+PF6-; MeO, (3)+ PF6-; Cl, (4)+PF6 -) react with equimolar quantities of (E)-4- (2-ferrocenylvinyl)-benzaldehyde, (E)-[(η5-Cp) Fe(η5-C5H4)-CH=CH-C 6H4CHO], to afford stereoselectively, the new homodimetallic hydrazones formulated as (E)-[(η5-Cp) Fe(η6-p-RC6H4)-NHN=CH- C6H4=CH-CH-(η5-C5 H4)Fe(η5-Cp)]+PF6 - (R=H, (5)+PF6-; Me, (6)+PF6-; MeO, (7)+PF 6-; Cl, (8)+PF6-). These compounds were fully characterized by elemental analysis and spectroscopic techniques (1H-and 13C-NMR, IR and UV-vis) and, in the case of complex (6)+PF6 -, by single crystal X-ray diffraction methods. The rotations of the ferrocenyl unit by 37.2 out of the -NHN-CH-C6H 4=CH-CH- spacer and coordinated phenyl ring planes, may generate an unfavorable structure to allow π-electron delocalization along the entire hydrazonato backbone between the two metals separated through bonds by more than 1.8 nm, as confirmed by the electrochemical data.

Idioma originalInglés
Páginas (desde-hasta)71-77
Número de páginas7
PublicaciónJournal of Organometallic Chemistry
Volumen660
N.º1
DOI
EstadoPublicada - 7 oct. 2002

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