Synthesis, crystal structure and characterizations of iron(III) and copper(II) complexes with the hydrazone ligand obtained from 2-formyl-pyridine and Girard's T reagent

Autor: Mihail D. Revenco, Rodolphe Clérac, Paulina Bourosh, Oleg Palamarciuc, Yurii A. Simonov, Janusz Lipkowski
Přispěvatelé: State University of Moldova, University of Moldova, Centre de recherches Paul Pascal (CRPP), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université Sciences et Technologies - Bordeaux 1, Institute of Applied Physics, Academy of Sciences of Moldova, Academy of Sciences of Moldova (ASM), Institute of Physical Chemistry, Polish Academy of Sciences, Polska Akademia Nauk = Polish Academy of Sciences (PAN)
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Zdroj: Inorganica Chimica Acta
Inorganica Chimica Acta, Elsevier, 2010, 363, pp. 2561-2566. ⟨10.1016/j.ica.2010.04.027⟩
ISSN: 0020-1693
DOI: 10.1016/j.ica.2010.04.027⟩
Popis: 6 pages; International audience; The condensation of 2-formyl-pyridine with Girard's T reagent yields a new hydrazone in the form of an ammonium quaternary salt: [H(2-PyGT)]Cl. This tridentate ligand is readily soluble in water and reacts with iron(III) or copper(II) chlorides to give [Fe(2-PyGT)Cl3] (1) or [Cu(2-PyGT)Cl2]-(H2O) (2) complexes, respectively. Single-crystal X-ray studies in 1 and 2 reveal that the coordination reaction gives rise to the deprotonation of the organic ligand that is coordinated using its NNO donor atoms in the form of a zwitterion species. The coordination spheres around the transition metal ions in complexes 1 and 2 are quite different. In 1, the iron site adopts a distorted octahedral coordination sphere, while the Cu(II) ions in 2 show a distorted tetragonal-pyramid geometry. As expected, the magnetic properties of these compounds reveal only weak antiferromagnetic interaction between spin carriers.
Databáze: OpenAIRE