58567-93-4Relevant articles and documents
Fluoro-Boron Complexes as Biocides: Synthetic, Structural and Biological Aspects
Saxena, Chitra,Singh, R. V.
, p. 707 - 711 (1994)
The present account deals with the synthesis, stereochemistry and biological properties of coordinatively saturated difluoroboron(III) compounds.The ligands used during the present investigations were prepared by the condensation of , , , and with 2-mercapto-aniline.The unimolar reactions between borontrifluoride-acetic acid and these ligands have produced BF2(NS) type of biologically active complexes.The quantitative and spectral analyses comprising u.v., i.r. and n.m.r. (1H, 11B, 13C and 19F) helped in establishing the structures of the resulting complexes.In the quest for better fungicides and bactericides, studies were conducted to assess the growth inhibiting potential of the synthesized complexes against various fungal and bacterial strains.The studies demonstrate that the concentration reached levels which are sufficient to inhibit and kill the pathogens.
Spectroscopic differences between heterocyclic benzothiazoline, -thiazole and imine containing ligands and comparison of the Co and Cu pyridine benzothiazole and imine complexes
Carlson, Lauren J.,Welby, Jenna,Zebrowski, Kelly A.,Wilk, Matthew M.,Giroux, Rachel,Ciancio, Nicole,Tanski, Joseph M.,Bradley, Amy,Tyler, Laurie A.
experimental part, p. 159 - 166 (2011/03/21)
Five heterocyclic benzothiazoline and -thiazole analogs have been synthesized and characterized by 1H NMR and IR spectroscopy. The analogs fall into two different classes, (a) those which contain one benzothiazoline group adjacent to the hetero
