Electrochemical synthesis of cobalt, nickel, copper, zinc and cadmium complexes with N[(2-hydroxyphenyl)methylidine]N '-tosylbenzene-1,2-diamine. Thecrystal structures of {(1,10-phenanthroline)[N-(2-oxophenyl)methylidine]-N-tosylbenzene-1,2-diaminato}nickel(II) and {(1,10-phenanthroline)[N-(2-oxophenyl)methylidine]-N '-tosylbenzene-1,2-diaminato}copper(II)

Citation
M. Bernal et al., Electrochemical synthesis of cobalt, nickel, copper, zinc and cadmium complexes with N[(2-hydroxyphenyl)methylidine]N '-tosylbenzene-1,2-diamine. Thecrystal structures of {(1,10-phenanthroline)[N-(2-oxophenyl)methylidine]-N-tosylbenzene-1,2-diaminato}nickel(II) and {(1,10-phenanthroline)[N-(2-oxophenyl)methylidine]-N '-tosylbenzene-1,2-diaminato}copper(II), INORG CHIM, 295(1), 1999, pp. 39-47
Citations number
35
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
INORGANICA CHIMICA ACTA
ISSN journal
00201693 → ACNP
Volume
295
Issue
1
Year of publication
1999
Pages
39 - 47
Database
ISI
SICI code
0020-1693(19991115)295:1<39:ESOCNC>2.0.ZU;2-1
Abstract
The electrochemical oxidation of cobalt, nickel, copper, zinc or cadmium an odes in an acetonitrile solution containing N[(2-hydroxyphenyl)methylidine] -N'-tosylbenzene-1,2-diamine (H2L) yielded compounds of general formula [ML ]. When 1,10-phenanthroline (phen) or 2,2'-bipyridine (bipy) is added to th e cell, mixed ligand complexes are obtained. The crystal structures of {(1, 10-phenanthroline)[N-(2-oxophenyl)methylidine]-N'-tosylbenzene-1,2-diaminat o}nickel(II) (1) and {(1,10-phenanthroline)-[N-(2-oxophenyl)methylidine]-N' -tosylbenzene-1,2-diaminato} copper(II) (2) were determined by X-ray diffra ction. Compound 1 consists of a binuclear [Ni2L21(phen)(2)] complex with ph enolic oxygen atoms bridging both nickel atoms. Each nickel atom is in a di storted octahedral [NiN4O2] environment. Compound 2 is monomeric, with the copper atom in a [CuN4O] distorted square pyramidal geometry. The electroni c, IR and NMR spectra of the complexes are discussed and related to the str ucture. (C) 1999 Elsevier Science S.A. All rights reserved.