Issue 9, 2005

Structural and spectroscopic studies on mercury(ii) tribenzylphosphine complexes

Abstract

The tribenzylphosphine (PBz3) complexes of mercury(II), [Hg(PBz3)2](BF4)2, [Hg(PBz3)2(NO3)2] and [HgX(NO3)(PBz3)] (X = Cl, Br, I and SCN), have been synthesised and their structures determined by single-crystal X-ray crystallography. [Hg(PBz3)2](BF4)2 contains [Hg(PBz3)2]2+ cations with linear P–Hg–P coordination, the first example of a truly two-coordinate [Hg(PR3)2]2+ complex. The mercury coordination in [Hg(PBz3)2(NO3)2] can be described as distorted tetrahedral, with a significant deviation of the P–Hg–P angle from linearity as a result of coordination of the nitrate groups. Nitrate coordination is also observed in [HgX(NO3)(PBz3)] (X = Cl, Br, I), resulting in significantly non-linear P–Hg–X coordination. The thiocyanate complex is a centrosymmetric thiocyanate-bridged dimer with distorted trigonal-pyramidal mercury coordination to the P atom of PBz3, to the S and N atoms of two bridging thiocyanate groups, and to the O atom of one nitrate group. For all the nitrato complexes, secondary mercury-nitrate interactions (Hg–O 2.7–3.1 Å) effectively raise the coordination number of the Hg(II) centres to six. High-resolution 31P solid-state NMR spectra of the six tribenzylphosphine mercury(II)-complexes, obtained by combining magic-angle spinning, proton dipolar decoupling and proton–phosphorus cross-polarization (CP-MAS), have been recorded. The spectra of [Hg(PBz3)2](BF4)2 and [HgX(NO3)(PBz3)] (X = Cl, Br, I and SCN) exhibit a single line, due to species that contain non-magnetic isotopes of mercury, and satellite lines, due to 1J(31P–199Hg) coupling. The asymmetric unit of [Hg(PBz3)2(NO3)2] contains two molecules with four phosphorus environments, resulting in two AB spectra with 2J(31P–31P) coupling, due to species that contain non-magnetic isotopes of mercury, and satellite lines consisting of two ABX spectra, due to 1J(31P–199Hg) coupling. These spectra have been analysed to yield all of the chemical shifts and coupling constants involved. A remarkable increase in 1J(31P–199Hg) is observed from [Hg(PBz3)2](BF4)2 to [Hg(PBz3)2(NO3)2] as a consequence of the incorporation of the nitrate group into the Hg coordination sphere in the latter case. Several of the spectra also exhibit broader satellites due to the presence of scalar spin–spin coupling between 31P and the quadrupolar 201Hg nucleus. Slow-spinning methods have been used to analyze the spinning-sideband intensities of the NMR spectra, in order to obtain the 31P shielding anisotropy and asymmetry parameters Δσ and η. The 199Hg and 31P NMR shielding tensors of PMe3 models of the above six compounds have been calculated using relativistic density functional theory. The 31P results are in good agreement with experiment and assist in the assignment of some of the signals.

Graphical abstract: Structural and spectroscopic studies on mercury(ii) tribenzylphosphine complexes

Supplementary files

Article information

Article type
Paper
Submitted
23 Dec 2004
Accepted
09 Mar 2005
First published
31 Mar 2005

Dalton Trans., 2005, 1602-1612

Structural and spectroscopic studies on mercury(II) tribenzylphosphine complexes

G. A. Bowmaker, B. Assadollahzadeh, A. M. Brodie, E. W. Ainscough, G. H. Freeman and G. B. Jameson, Dalton Trans., 2005, 1602 DOI: 10.1039/B419253B

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