Abstract
The reaction of Hg(O 3SCF 3) 2 with bis(diphenylphosphino)amine, Ph 2PNHPPh 2 (dppam), produces the novel, rare face-to-face complex [Hg 2(O 3SCF 3) 4(dppam) 2] ( 1). Treatment of 1 with Na 2N 2O 3 leads to trans-[Hg{Ph 2PNP(O)Ph 2- P, O} 2] ( 2) via regioselective oxidation and simultaneous deprotonation of dppam. 2 is the first true square-planar Hg(II) compound. In 2 the coordination plane and the five-membered rings of the HgNOP 2 moieties are completely coplanar indicating strong π-bonding interactions. Both 1 and 2 have been fully characterized by X-ray structure analyses, NMR spectroscopy ( 199 Hg{ 1 H}, 31 P{ 1 H}, 13 C{ 1 H}, 1 H) , ESI and FAB mass spectrometry, IR spectroscopy, elemental analyses, and melting points. Since in Hg(II) compounds relativistic effects favour linear coordination and Hg(II) donor atom preferences play a significant role, the Hg–P bond length of 2.4042(7) Å in 2 is short, whereas the Hg–O bond length of 2.7138(15) Å is long. In view of the X-ray structures of 1 and 2, it is shown that the delocalized charge in [Ph 2PNP(O)Ph 2] − is responsible for the achievement of the square-planar coordination in a Hg(II) compound. A similar π-bonding effect has been observed in several square-planar complexes of Pt(II), Pd(II), and Ni(II) containing cis-1,2-bis(diphenylphosphino)ethene ( cis-dppen).
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