REDISTRIBUTION REACTIONS OF DIORGANOTIN DICARBOXYLATES AND DIORGANOTIN DIHALIDES - A CONVENIENT METHOD FOR THE PREPARATION OF HALO-DIORGANOTIN CARBOXYLATES
S. Ali et al., REDISTRIBUTION REACTIONS OF DIORGANOTIN DICARBOXYLATES AND DIORGANOTIN DIHALIDES - A CONVENIENT METHOD FOR THE PREPARATION OF HALO-DIORGANOTIN CARBOXYLATES, Heteroatom chemistry, 8(3), 1997, pp. 273-278
Organotin compounds with R-2(X)SnL (where R = Me, Et, n-Bu, Ph; L = th
e trans-3-(2-furanyl)-2-propenoate anion or the trans-3-(3-methylpheny
l)-2-propenoate anion; and X = Cl) have been prepared by redistributio
n reactions between the R2SnL2 and R2SnX2 compounds. These compounds w
ere characterized by elemental analyses and various spectroscopic tech
niques such as H-1, C-13, Sn-119 NMR, Mass, Mossbauer, and IR spectros
copies. On the basis of these spectroscopic data, it is suggested that
these compounds adopt the cis-R-2(X)SnO2 geometry. (C) 1997 John Wile
y & Sons, Inc.