L. Nagy et al., PREPARATION AND STRUCTURAL STUDIES ON ORGANOTIN(IV) COMPLEXES WITH FLAVONOIDS, Journal of radioanalytical and nuclear chemistry, 227(1-2), 1998, pp. 89-98
Fourteen complexes of di-n-butyltin(IV)(2+) cations with flavonoid gly
cosides (rutin, hesperidin, 2',4',3-trihydroxy-5',4-dimetoxychalkone 4
-rutinoside) and flavonoid aglycones (quercetin, morin, hesperitin and
sorte flavones) were prepared. The composition of the complexes was d
etermined by standard analytical methods. The results showed that comp
lexes containing diorganotin(lV)(2+) moiety and the ligand in 1:1, 2:1
or 3:1 ratio are formed. The FTIR spectra were consistent with the pr
esence of Sn-O (phenol or carbohydrate) vibration in the compounds. Th
e structure of the complexes was measured by Mossbauer spectroscopy. C
omparison of the experimental quadrupole splitting with those calculat
ed on the basis of partial quadrupole splitting concept revealed that
the complexes are of four types: with the central tin atoms surrounded
by donor atoms in a purely trigonal-bipyramidal, octahedral+trigonal-
bipyramidal, trigonal-bipyramidal+tetrahedral and octahedral+tetrahedr
al arrangement. This procedure also distinguished between the differen
t structural isomers of both trigonal-bipyramidal and octahedral compl
exes. Conclusions could therefore be drawn on the factors determining
which of the isomers are formed in the systems. The Mossbauer paramete
rs obtained for organotin(rv)-flavonoid complexes were compared with t
hose measured for organotin(IV)-carbohydrate complexes.