[{CpFe(CO) 2 } 2 l-(NH 2 (CH 2 ) n NH 2 )](BF 4 ) 2 (n = 2-4) (3), respectively. These complexes have been fully characterized and the mass spectral patterns of complexes 2 are reported. The structures of compounds 2a (n = 2) and 2b (n = 3) have been confirmed by single crystal X-ray crystallography. The single crystal X-ray diffraction data show that complex 2a, [CpFe(CO) 2 NH 2 (CH 2 ) 2 CH 3 ]BF 4 , crystallizes in a triclinic P 1 space group while 2b, [CpFe(CO) 2 NH 2 (CH 2 ) 3 CH 3 ]BF 4 , crystallizes in an orthorhombic Pca2 1 space group with two crystallographically independent molecular cations in the asymmetric unit. Furthermore, the reaction of 1 with 1-alkenes gives the g 2 -alkene complexes in high yield.
Key indicators: single-crystal X-ray study; T = 100 K; mean (C-C) = 0.003 Å; R factor = 0.033; wR factor = 0.084; data-to-parameter ratio = 18.0.The asymmetric unit of the title compound, [Fe 2 (C 5 H 5 ) 2 -(C 2 H 8 N 2 )(CO) 4 ](BF 4 ) 2 , contains two half-cations, each located on a center of symmetry, and two tetrafluoridoborate anions. The iron atoms adopt a three-legged piano-stool geometry. All amine H atoms are involved in N-HÁ Á ÁF hydrogen bonds, which consolidate the crystal packing along with weak C-HÁ Á ÁO and C-HÁ Á ÁF interactions.
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