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Oxidation of (η5-6-exo-cyclopentadienylcyclohexadienyl)- (η5-cyclopentadienyl) iron by trityl hexafluorophosphateby trityl hexafluorophosphate
Authors:L N Novikova  I V Shchirina-Eingorn  N A Ustynyuk  P V Petrovskii  L I Denisovich
Institution:(1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation
Abstract:Oxidation of the cyclohexadienyl complex Fe(η5-C5H5)(1-5-75-6-exo-C5H5-C6H6) (2) by (Ph3C)PF6 (CH2Cl2, from −30 to +20 °C) occurs as two concurrent processes: elimination of an H atom from the cyclohexadienyl ligand and replacement of an H atom in the cyclopentadienyl ring by a CPh3 fragment. A mixture of cationic complexes Fe(η5-C5H5) (η6-Ph-C5H5]+ (1+) and Fe(η5-C5H4CPh3) (η6-Ph-C5H5]+ (4+) (4 +) with PF6 anions is obtained. Deprotonation of the mixture of 1+ and 4+ complexes under the action of Bu t OK inm-xylene followed by boiling of the reaction mixture gives phenylferrocene (7) as the product of η66 haptotropic rearrangement. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, NO. 5, pp. 1045–1047, May, 1997.
Keywords:alkylation  iron complexes  oxidation  interring haptotropic rearrangement
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