SYNTHESIS AND NMR-SPECTROSCOPY OF HLOROBIS(ACETOPHENONETHIOSEMICARBAZONE)MERCURY(II) FORMED FROM PHENYLMERCURY(II) CHLORIDE AND ACETOPHENONETHIOSEMICARBAZONE - THE FIRST EXAMPLE OF SYMMETRIZATION IN ORGANOMERCURY(II)-THIOSEMICARBAZONE CHEMISTRY
Ts. Lobana et al., SYNTHESIS AND NMR-SPECTROSCOPY OF HLOROBIS(ACETOPHENONETHIOSEMICARBAZONE)MERCURY(II) FORMED FROM PHENYLMERCURY(II) CHLORIDE AND ACETOPHENONETHIOSEMICARBAZONE - THE FIRST EXAMPLE OF SYMMETRIZATION IN ORGANOMERCURY(II)-THIOSEMICARBAZONE CHEMISTRY, Inorganica Chimica Acta, 267(1), 1998, pp. 169-172
The reaction of phenylmercury(II) chloride with acetophenonethiosemica
rbazone (Hatsc) in ethanol in 1:1 mole ratio undergoes symmetrisation
forming the products, HgCl2(Hatsc)(2) and Ph2Hg instead of the anticip
ated compound PhHgCl(Hatsc). The analytical data, some physical proper
ties, IR and NMR (H-1, C-13, Hg-199) spectroscopy all support the form
ation of HgCl2(Hatsc)(2). Hg-199 NMR of the solid obtained from the fi
ltrate of the reaction provides evidence for Ph2Hg. This reaction repr
esents the first example of a symmetrisation phenomenon observed in or
ganomercury(II)-thiosemicarbazone chemistry. (C) 1998 Elsevier Science
S.A.