SYNTHESIS AND CHARACTERIZATION OF OXOTECHNETIUM(V) COMPLEXES WITH AZA-SUBSTITUTED 2,6-DIMETHYL-4-AZAHEPTANE-2,6-DITHIOL LIGANDS AND BENZYL MERCAPTAN AS COLIGAND
Dm. Spyriounis et al., SYNTHESIS AND CHARACTERIZATION OF OXOTECHNETIUM(V) COMPLEXES WITH AZA-SUBSTITUTED 2,6-DIMETHYL-4-AZAHEPTANE-2,6-DITHIOL LIGANDS AND BENZYL MERCAPTAN AS COLIGAND, Inorganic chemistry, 34(5), 1995, pp. 1077-1082
The design and synthesis of mixed oxotechnetium(V)-99 complexes with a
novel series of aza-substituted 2,6-dimethyl-4-azaheptane-2,6-dithiol
ligands of the general type NS2 and benzyl mercaptan as coligand are
reported. Ligands (general formula R-CH2CH2N[CH2C(CH3)(2)SH](2) with R
= N(C2H5)(2), piperidin-1-yl, pyrrolidin-1-yl, and morpholin-4-yl) we
re synthesized through the reduction of aza-substituted heterocyclic a
za disulfides which result from the reductive cyclization of 2.2'-dith
iobis(2-methylpropanal) with the appropriate primary amine. The Tc-99
complexes 5 (general formula TcO{[SC(CH3)(2)CH2](2)NCH(2)CH(2)R}X wher
e X = benzyl mercaptan) were prepared in high yield by the reaction of
Tc-99(V) gluconate with a 1:1 mixture of the appropriate tris-chelati
ng ligand and the monodentate benzyl mercaptan. The resulting complexe
s were purified through flash column chromatography. Crystals were for
med by dissolving complexes in a mixture of MeOH/water and slowly evap
orating the solvents. Complexes were characterized by elemental analys
es and spectroscopic methods. Complete assignments of H-1 and C-13 NMR
resonances were made for all complexes. X-ray crystallographic analys
is of 5d (C21H35N2S3O2TC, R = morpholin-4-yl) showed that the complex
crystallizes in the monoclinic space group P2(1)/c with a 17.166(2) An
gstrom, b = 8.9282(7) Angstrom, c = 17.738(2) Angstrom, beta = 116.031
(3)degrees, V = 2442.7(4) Angstrom(3), and Z = 4. Complex 5d has trigo
nally distorted square pyramidal coordination geometry around techneti
um with the side chain on nitrogen directed toward the oxygen of the T
c=O core (syn configuration). The nOe data confirm that in all cases t
he major isolated product of the synthesis has the syn configuration o
f the side chain.