[2-(N,N-Dimethylaminomethyl)ferrocenyl] as a ligand towards mercury
摘要:
The diorganomercurial bis[2-(NN-dimethylaminomethyl)ferrocenyl]mercury(II), (FcN)(2)Hg (3), can be obtained by the symmetrisation of the heteroleptic (FcN)HgCl (2) with Na2S2O3 or in the transmetallation reaction of 2 with (FcN)Li. By crystallisation only the crystals of rac-(FcN)(2)Hg were obtained. X-ray diffraction analysis revealed linear coordinated mercury atom with two eta (1)-bonded FcN ligands. Additionally, weak chelate interactions exist between mercury and nitrogen atoms of the -CH2NMe2 side chains. According to the H-1-NMR findings, these interactions are not preserved in solution. Diorganomercurial 3 appears in solution as a mixture of two diastereomers with rac/meso-(FcN)(2)Hg ratio of 1:1. This diastereomeric ratio in solution remains constant within a wide temperature range and in different solvents. The NMR spectroscopic data of the heteroleptic organomercurials [(FcN)HgCl](2).H2O (1) and (FcN)HgCl (2) indicate the chelate-free structure of this compounds in solution within the studied temperature interval (- 80 to 90 degreesC). (C) 2001 Elsevier Science B.V. All rights reserved.
[2-(N,N-Dimethylaminomethyl)ferrocenyl] as a ligand towards mercury
摘要:
The diorganomercurial bis[2-(NN-dimethylaminomethyl)ferrocenyl]mercury(II), (FcN)(2)Hg (3), can be obtained by the symmetrisation of the heteroleptic (FcN)HgCl (2) with Na2S2O3 or in the transmetallation reaction of 2 with (FcN)Li. By crystallisation only the crystals of rac-(FcN)(2)Hg were obtained. X-ray diffraction analysis revealed linear coordinated mercury atom with two eta (1)-bonded FcN ligands. Additionally, weak chelate interactions exist between mercury and nitrogen atoms of the -CH2NMe2 side chains. According to the H-1-NMR findings, these interactions are not preserved in solution. Diorganomercurial 3 appears in solution as a mixture of two diastereomers with rac/meso-(FcN)(2)Hg ratio of 1:1. This diastereomeric ratio in solution remains constant within a wide temperature range and in different solvents. The NMR spectroscopic data of the heteroleptic organomercurials [(FcN)HgCl](2).H2O (1) and (FcN)HgCl (2) indicate the chelate-free structure of this compounds in solution within the studied temperature interval (- 80 to 90 degreesC). (C) 2001 Elsevier Science B.V. All rights reserved.