SYNTHESIS AND CHARACTERIZATION OF COMPLEXES OF TRIALKYLPHOSPHINE AND TRIARYLPHOSPHINE GOLD(I) WITH THIOLATED PURINES AND PYRIMIDINES - A CLASS OF BIFUNCTIONAL COMPOUNDS WITH POTENTIAL ANTITUMOR-ACTIVITY
G. Stocco et al., SYNTHESIS AND CHARACTERIZATION OF COMPLEXES OF TRIALKYLPHOSPHINE AND TRIARYLPHOSPHINE GOLD(I) WITH THIOLATED PURINES AND PYRIMIDINES - A CLASS OF BIFUNCTIONAL COMPOUNDS WITH POTENTIAL ANTITUMOR-ACTIVITY, Inorganica Chimica Acta, 209(2), 1993, pp. 129-135
New complexes of the type R3PAuL or (R3PAu)2(mu-L) where R=ethyl or ph
enyl and L=6-thioguanine, 2,6-dithioxanthine, 2,4-dithiouracil and/or
dithioerythritol have been prepared. These complexes have been identif
ied by using elemental analysis, H-1, C-13 and P-31 NMR spectroscopy.
The structures have been proposed based on these spectroscopic studies
. Sulfur appears to be the binding site in disubstituted complexes of
2,4-dithiouracil and 1,4-dithioerythritol, while the phosphine gold(I)
moieties appear to be S and N bonded in 2,6-dithioxanthine and 6-thio
guanine. The potential use of these complexes as antitumor drugs is di
scussed.