RESUMO
The reaction of ferrocenylphenylcarbinol with the ethereal solution of boron trifluoride in dichloride methane resulted in the relevant ferrocenylphenylmethyl carbocation. Without separation from the reaction mixture, the ion reacted with ethanolamine to from N-(phenyl,ferrocenyl) methyl-beta-hydroxyethylamine(FcY). A series of coordinate complexes-FcY-Ni(II), FcY-Cu (II), FcY-Zn(II), FcY-Cd(II) and FcY-Hg(II) were obtained through coordination of this ligand with MCl2 (M = Ni, Cu, Zn, Cd, Hg). The complexes and ligand were taken for FTIR in the range of 4 000-400 cm(-1). Their major bonds were assigned and compared. The results showed that in all the complexes some bands (v(O-H), v(N-H) , delta(O-H), delta(N-H)) showed a certain shift to lower wave number, and bands(V(C-N), v(O-N)) exhibited a certain shift to higher wave number. The aminoalcohol groups and metal ions were bonding with coordinated bond.
RESUMO
alpha-Cyano-alpha-ferrocenylethoxytrimethylsilame was prepared by the addition of trimethysilyl cyanide to acetylferrocene. 2-Hydroxy-2-ferrocenylpropylamine(FcA) was synthesized by the reduction of alpha-cyano-alpha-ferrocenylethoxytrimethylsilame with lithium aluminum hydride. A series of coordinate complexes--FcA-Ni(II), FcA-Cu(II), FcA-Zn(II), FcA-Cd(II) and FcA-Hg(II) were obtained through coordination of this ligand with MCl2 (M= Ni, Cu, Zn, Cd and Hg). The FTIR spectra of the complexes and ligand were obtained in the range of 4 000-400 cm(-1). Their major bands were assigned and compared. The results showed that in all complexes some bands(upsilonO-H, upsilonN-H sigmaO-H, sigmaN-H) were shifted to lower wave number, and some(upsilonC-N, upsilonO-N) were shifted to higher wave number. The aminoalcohol groups and metal ions were bound with coordinated bond.