Abstract

Intramolecularly stabilized divalent mercury selenolates of empirical formula Hg(SeR)2[R = 2-Me2NCH2C6H41, (S)-2-Me2NCHMeC6H42, (R,S)-(C5H5)Fe(2-Me2NCHMeC5H3)3 and (S,R)-(C5H5)Fe(2-Me2NCHMeC5H3)4] have been synthesized in high yield by treating the corresponding diselenides with elemental mercury. The compounds show excellent solubility in non-polar solvents. They were characterized by elemental analysis, 1H, 13C, 77Se NMR, IR, Fourier-transform Raman and mass spectral techniques. The single-crystal structures of 1 and 4 were determined. Both are monomeric and the Hg atom is four-co-ordinate, being bound to a pair of chelating aminoselenolate ligands with both the six-membered rings having Se–Hg–N co-ordination adopting an envelope conformation. The bond configuration about Hg in 1 can be approximated to distorted tetrahedral, while in 4 it is more square planar with the two Se atoms being mutually trans and the Se–Hg–Se angle 168.6(2)°. Compounds 1 and 2 vaporize without decomposition at atmospheric pressure and decompose at higher temperatures to give HgSe while 3 decomposes to HgSe.

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