Nickel(II) Complexes of Some Quadridentate Schiff Base Ligands I
Abstract
A series of nickel(II) complexes, NiL, of the Schiff bases formed by condensation of 5-chloro-2-hydroxybenzophenone with a series of alkanediamines, NH 2(CH 2) nNH 2 (n = 2-12), have been synthesized and their physicochemical properties investigated. Unlike their salicylaldimine analogs, the NiL complexes derived from long-chain alkanediamines are highly soluble in nondonor solvents. In nondonor solvents these complexes are low-spin planar monomers with the Schiff bases acting as quadridentate ligands, although there is a small degree of molecular association in some cases. In the solid state, some of the complexes (n = 5-12) contain both octahedral and square-planar Ni(II) usually in the ratio 1:2, and a trimeric structure has been proposed to account for this behavior. For n = 3-12, the complexes reversibly form bis-pyridine adducts: NiL + 2C 5H 5N ⇄ NiL·2C 5H 5N. The solid pyridine adducts were isolated from pyridine solution as paramagnetic solids and these complexes are assigned a trans-octahedral structure. A square-pyramidal complex, NiL·H 2O, has been isolated for n = 4.
Recommended Citation
G. M. Mockler et al., "Nickel(II) Complexes of Some Quadridentate Schiff Base Ligands I," Inorganic Chemistry, American Chemical Society (ACS), Jan 1972.
The definitive version is available at https://doi.org/10.1021/ic50112a030
Department(s)
Chemistry
International Standard Serial Number (ISSN)
0020-1669
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 1972 American Chemical Society (ACS), All rights reserved.
Publication Date
01 Jan 1972