Conclusions
-
1.
The σ-allyl complex Cp (CO)2FeCH2C(Fc)=C (CN)2 reacts with iodine to give products resulting from cleavage to the Fe-C σ-bond by iodine, and also an addition product of iodine to the double bond of the allyl ligand, but is stable with respect to hydrogen chloride, sulfur trioxide, and tetracyanoethylene.
-
2.
The C-Fe σ-bond in Cp(CO)2FeCH2C (Fc)=C(CN)2 is easily cleaved by nucleophilic reagents (LiAlH4 and LiC5H4Mn(CO)3).
-
3.
Reaction of (CN)2C=C(Fc)CH2I with Cp(CO)2FeNa gave (CN)2C=C(Fc)CH3 and CP(CO)2FeI,
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Translated from Izvestiya Akademii Nauk SSSR, No. 10, pp. 2302–2307, October, 1986.
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Leont'eva, L.I., Bek, V., Kravtsov, D.N. et al. Reactions of 3,3-dicyano-2-ferrocenylallyl(cyclopentadienyl)dicarbonyliron with electrophilic and nucleophilic reagents. Russ Chem Bull 35, 2105–2110 (1986). https://doi.org/10.1007/BF00957534
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DOI: https://doi.org/10.1007/BF00957534