ic980296y_si_001.cif (36.26 kB)
Correlation of a Solution-State Conformational Change between Mercuric Chloride Complexes of Tris[(2-(6-methylpyridyl))methyl]amine with X-ray Crystallographic Structures
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posted on 1998-08-20, 00:00 authored by Deborah C. Bebout, James F. Bush, Kathleen K. Crahan, Margaret E. Kastner, Damon A. ParrishSolution-state NMR and X-ray crystallography were used to investigate the complexation of HgCl2 by the potentially
tetradentate ligand tris[(6-methyl-2-pyridyl)methyl]amine (TLA) in acetonitrile. A change in the ligand
conformation as a function of the metal-to-ligand ratio could be indirectly monitored through large changes in
3J(1H199Hg) to the methylene protons at −40 °C. The solution-state NMR were correlated with two solid-state
structures. The five-coordinate complex [Hg(TLA)Cl2] (1) crystallizes in the triclinic space group P1̄ with a =
8.663(3) Å, b = 11.539(4) Å, c = 13.739(3) Å, α = 80.81(2)°, β = 75.84(2)°, γ = 80.97(3)°, and Z = 2. The
Hg−Namine distance of 2.505(7) Å for the tridentate ligand is the same as the average Hg−Nlutidyl distance of
2.50(3) Å for the two bound lutidyl nitrogens. [Hg(TLA)Cl]2(Hg2Cl6) (2) also crystallizes in P1̄ with a = 10.606(2) Å, b = 15.104(3) Å, c = 17.785(4) Å, α = 67.46(3)°, β = 83.52(3)°, γ = 80.29(3)°, and Z = 2. The ligand
is tetradentate in the two crystallographically unique cations which are arranged in a dimer-like orientation. The
average Hg−Cl distance is 2.37 (1) Å, and the average interionic Hg−Cl distance is 3.51(1) Å. The Hg− Nlutidyl
distances are of two types: two have an average distance of 2.36(3) Å, nearly the same as the Hg−Namine distance
of 2.35(2) Å. The remaining four Nlutidyl distances have an average distance of 2.56(5) Å.