C. Saxena et Rv. Singh, FLUORO-BORON COMPLEXES AS BIOCIDES - SYNTHETIC, STRUCTURAL AND BIOLOGICAL ASPECTS, Journal fur praktische Chemie, Chemiker-Zeitung, 336(8), 1994, pp. 707-711
The present account deals with the synthesis, stereochemistry and biol
ogical properties of coordinatively saturated difluoroboron(III) compo
unds. The ligands used during the present investigations were prepared
by the condensation of [1-(thien-2-yl)-ethanone], [1-(pyridin-2-yl)et
hanone], [1-(furan-2-yl)ethanone], [1-(naphthen-2-yl)ethanone] and [(t
hien-2-yl)methanal] with 2-mercapto-aniline. The unimolar reactions be
tween borontrifluoride-acetic acid and these ligands have produced BF2
(NS) type of biologically active complexes. The quantitative and spect
ral analyses comprising u.v., i.r. and n.m.r. (H-1, B-11, C-13 and F-1
9) helped in establishing the structures of the resulting complexes. I
n the quest for better fungicides and bactericides, studies were condu
cted to assess the growth inhibiting potential of the synthesized comp
lexes against various fungal and bacterial strains. The studies demons
trate that the concentration reached levels which are sufficient to in
hibit and kill the pathogens.