Visible light irradiation of cation [(η5-C6H7)Fe(η-C6H6)]+ (1+) in acetonitrile results in substitution of the benzene ligand giving the labile acetonitrile derivative [(η5-C6H7)Fe(MeCN)3]+ (2a+). The stable isonitrile and phosphite complexes [(η5-C6H7)FeL3]+ [L = tBuNC (2b+), P(OMe)3 (2c+), P(OEt)3 (2d+)] were obtained by reaction of 1 with L in MeCN. The structures of 2cPF6, [CpFe(η-C6H6)]PF6 (3PF6), and Cp∗Fe(η-C6H6)]PF6 (4PF6) were determined by X-ray diffraction. The redox activity of the cyclohexadienyl complexes 1+, 2b+−2d+ has been investigated by electrochemical techniques and compared with that of the related cyclopentadienyl complexes 3+ and 4+. DFT calculations of the redox potentials and the respective geometrical changes were performed. Variable temperature Mössbauer (ME) spectroscopy has elucidated the relationship between structure and formal oxidation state of the iron atom in these complexes. In the case of 3+ an unexpected pair of crystallographic changes has been observed and interpreted in terms of both a second and first order phase transition. The mean-square-amplitude-of-vibration of the metal atom has been compared between the ME and X-ray data. ME measurements in a magnetic field have shown that in 4+ the quadrupole splitting is positive as it is in ferrocene.

Zanello, P., Herber, R.H., Kudinov, A.R., Corsini, M., FABRIZI DE BIANI, F., Nowik, I., et al. (2009). Synthesis, structure, electrochemistry, and Mossbauer effect studies of (ring)Fe complexes (ring = Cp, Cp*, and C(6)H(7)). Photochemical replacement of benzene in the cyclohexadienyl complex [(eta(5)-C(6)H(7))Fe(eta-C(6)H(6))](+). JOURNAL OF ORGANOMETALLIC CHEMISTRY, 694, 1161-1171 [10.1016/j.jorganchem.2008.09.028].

Synthesis, structure, electrochemistry, and Mossbauer effect studies of (ring)Fe complexes (ring = Cp, Cp*, and C(6)H(7)). Photochemical replacement of benzene in the cyclohexadienyl complex [(eta(5)-C(6)H(7))Fe(eta-C(6)H(6))](+)

ZANELLO, PIERO;CORSINI, MADDALENA;FABRIZI DE BIANI, FABRIZIA;
2009-01-01

Abstract

Visible light irradiation of cation [(η5-C6H7)Fe(η-C6H6)]+ (1+) in acetonitrile results in substitution of the benzene ligand giving the labile acetonitrile derivative [(η5-C6H7)Fe(MeCN)3]+ (2a+). The stable isonitrile and phosphite complexes [(η5-C6H7)FeL3]+ [L = tBuNC (2b+), P(OMe)3 (2c+), P(OEt)3 (2d+)] were obtained by reaction of 1 with L in MeCN. The structures of 2cPF6, [CpFe(η-C6H6)]PF6 (3PF6), and Cp∗Fe(η-C6H6)]PF6 (4PF6) were determined by X-ray diffraction. The redox activity of the cyclohexadienyl complexes 1+, 2b+−2d+ has been investigated by electrochemical techniques and compared with that of the related cyclopentadienyl complexes 3+ and 4+. DFT calculations of the redox potentials and the respective geometrical changes were performed. Variable temperature Mössbauer (ME) spectroscopy has elucidated the relationship between structure and formal oxidation state of the iron atom in these complexes. In the case of 3+ an unexpected pair of crystallographic changes has been observed and interpreted in terms of both a second and first order phase transition. The mean-square-amplitude-of-vibration of the metal atom has been compared between the ME and X-ray data. ME measurements in a magnetic field have shown that in 4+ the quadrupole splitting is positive as it is in ferrocene.
2009
Zanello, P., Herber, R.H., Kudinov, A.R., Corsini, M., FABRIZI DE BIANI, F., Nowik, I., et al. (2009). Synthesis, structure, electrochemistry, and Mossbauer effect studies of (ring)Fe complexes (ring = Cp, Cp*, and C(6)H(7)). Photochemical replacement of benzene in the cyclohexadienyl complex [(eta(5)-C(6)H(7))Fe(eta-C(6)H(6))](+). JOURNAL OF ORGANOMETALLIC CHEMISTRY, 694, 1161-1171 [10.1016/j.jorganchem.2008.09.028].
File in questo prodotto:
File Dimensione Formato  
1-s2.0-S0022328X08005792-main.pdf

non disponibili

Tipologia: Post-print
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 1.05 MB
Formato Adobe PDF
1.05 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/23745
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo