Lm. Epstein et al., ORGANOMETALLIC CHEMISTRY - THE STRUCTURE OF ARYLMERCURY DERIVATIVES OF ALIZARIN AND THEIR INTERACTION WITH ANIONS, Russian chemical bulletin, 43(11), 1994, pp. 1908-1912
The structure of mono- and di-ArHg-derivatives of alizarin (1,2-dihydr
oxy-9,10-anthraquinone) and their interactions with halide- and oxygen
-containing salts are examined by vibrational and electronic spectrosc
opy. The interaction of solid mono- and di-ArHg-derivatives of alizari
n with bromides results only in the formation of the monoanion or the
ion pair, depending on the nature of the counterion. Dianions are form
ed in a DMSO solution with very great excess of the bromide.