2000
DOI: 10.1016/s0040-4039(00)00456-1
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Convenient access to new mono- and dinuclear organometallic hydrazones from [(η5-Cp)Fe(η6-arylhydrazine)]+

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Cited by 13 publications
(39 citation statements)
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“…À that are present in the same asymmetric unit, and its solution dynamics that reveal the two rotational barriers of the sandwich moieties about the -N(H)-N=C(Me)-spacer; and (iv) finally, DFT calculations on the [9] 2þ=þ=0 series as well as on related mononuclear models, which provide a theoretical rationalization of the electronic interaction between the metal centers. Some of the experimental results have been previously communicated.…”
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confidence: 99%
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“…À that are present in the same asymmetric unit, and its solution dynamics that reveal the two rotational barriers of the sandwich moieties about the -N(H)-N=C(Me)-spacer; and (iv) finally, DFT calculations on the [9] 2þ=þ=0 series as well as on related mononuclear models, which provide a theoretical rationalization of the electronic interaction between the metal centers. Some of the experimental results have been previously communicated.…”
mentioning
confidence: 99%
“…All the new compounds were characterized by elemental analysis and IR, UV-Vis and 1 H NMR spectroscopies. For compound [9] þ PF 6 À , the activation energy DG # for the hindered rotations of the mixed sandwich [CpFe(Z 6 -C 6 H 5 -)] þ (41.8 ± 0.9 and 41.2 ± 3.7 kJ mol À1 ) and the ferrocenyl unit (40.0 ± 3.2 kJ mol À1 ) about the -NH-N=CMe-hydrazone backbone have been determined by variable temperature 1 H NMR spectroscopic studies. The electrochemical behavior of the dinuclear hydrazones was explored by cyclic voltammetry, and features the role of the cationic [CpFe(Z 6 -arene)] þ moiety as an electron acceptor.…”
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confidence: 99%
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