COMPLEXES OF A NEW BIDENTATE CHELATING PYRIDYL SULFONAMIDE LIGAND WITH COPPER(II), COBALT(II) AND PALLADIUM(II) - CRYSTAL-STRUCTURES AND SPECTROSCOPIC PROPERTIES/
Ca. Otter et al., COMPLEXES OF A NEW BIDENTATE CHELATING PYRIDYL SULFONAMIDE LIGAND WITH COPPER(II), COBALT(II) AND PALLADIUM(II) - CRYSTAL-STRUCTURES AND SPECTROSCOPIC PROPERTIES/, Inorganica Chimica Acta, 278(2), 1998, pp. 178-184
Reaction of the bidentate ligand 2-(2-aminophenyl) pyridine with p-tol
uenesulfonyl chloride afforded the new bidentate ligand HL which conta
ins potentially chelating pyridyl and (protonated) sulfonamide N-donor
binding sites. The crystal structure of the ligand shows that the sul
fonamide NH proton is involved in a hydrogen-bonding interaction with
the pyridyl N atom, resulting in a near-coplanar arrangement of the py
ridyl and phenyl rings. Reaction of HL with various metal(II) acetates
(M = Cu, Co, Pd) affords the neutral complexes [ML2] in each case in
which the sulfonamide is deprotonated. All of these have been crystall
ographically characterised; the Cu(II) and Pd(II) complexes are planar
, whereas the Co(II) complexes is pseudo-tetrahedral with the two CoN2
planes at 85 degrees to one another. Appropriate spectroscopic and el
ectrochemical studies on the complexes are described. (C) 1998 Elsevie
r Science S.A. All rights reserved.