Four novel mononuclear and polynuclear Cu(I) thiosaccharinates with triphenylphosphane and bis(diphenylposphino)methane. Synthesis and structural study of Cu(4)(tsac)(4)(PPh(3))(3), Cu(tsac)(PPh(3))(2), Cu(4)(tsac)(4)(dppm)(2), and Cu(2)(tsac)(2)(dppm)(2)
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
---|---|
Data(s) |
20/10/2012
20/10/2012
2009
|
Resumo |
Four new ternary complexes of copper(I) with thiosaccharin and phosphanes were prepared. The reaction of [Cu(4)(tsac)(4)(CH(3)CN)(2)] (1) (tsac: thiosaccharinate anion) with PPh(3) in molar ratios Cu(I)/PPh(3) 1:075 and 1:2 gave the complexes [Cu(4)(tsac)(4)(PPh(3))(3)] center dot CH(3)CN (2) and Cu(tsac)(PPh(3))(2) (3), respectively. The reaction of 1 with Ph(2)PCH(2)PPh(2) (dppm) in molar ratios Cu(I)/dppm 2:1 and 1:1 gave the complexes [Cu(4) (tsac)(4)(dppm)(2)] center dot 2CH(2)Cl(2) (4) and [Cu(2)(tsac)(2)(dppm)(2)] center dot CH(2)Cl(2) (5), respectively. All the compounds have been characterized by spectroscopic and X-ray crystallographic methods. Complex 2 presents a tetra-nuclear arrangement with three metal centers in distorted tetrahedral S(2)NP environments, the fourth one with the Cu(I) ion in a distorted trigonal S(2)N coordination sphere, and the tsac anions acting as six electron donor ligands in mu(3)-S(2)N coordination forms. Complex 3 shows mononuclear molecular units with copper(I) in a distorted trigonal planar coordination sphere, built with the exocyclic S atom of a mono-coordinated thiosaccharinate anion and two P-atoms of triphenylphosphane molecules. With dppm as secondary ligand the structures of the complexes depends strongly on the stoicheometry of the preparation reaction. Complex 4 has a centrosymmetric structure. Two triply bridged Cu(2)(tsac)(2)(dppm) units are joined together by the exocyclic S-atoms of two tsac anions acting effectively as bridging tridentate ligands. Complex 5 is conformed by asymmetric dinuclear moieties where the two dppm and one tsac ligands bridge two Cu(I) atoms and the second tsac anion binds one of the metal centers through its exocyclic S-atom. (C) 2009 Elsevier B.V. All rights reserved. Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET) CONICET, Argentina FAPESP, Brazil Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) SGCyT-UNS SGCyT-UNS[M24/Q025] |
Identificador |
INORGANICA CHIMICA ACTA, v.362, n.8, p.2900-2908, 2009 0020-1693 http://producao.usp.br/handle/BDPI/29945 10.1016/j.ica.2009.01.014 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE SA |
Relação |
Inorganica Chimica Acta |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE SA |
Palavras-Chave | #Copper(I) #Thiones #Thionates #Phosphanes #X-ray crystal structure #Spectra #BINUCLEAR COPPER(I) COMPLEXES #HETEROCYCLIC THIONE LIGANDS #X-RAY-DIFFRACTION #CRYSTAL-STRUCTURE #ELECTROCHEMICAL SYNTHESIS #SILVER(I) COMPLEXES #SPECTROSCOPIC CHARACTERIZATION #MOLECULAR-STRUCTURE #BUTTERFLY CLUSTERS #BRIDGING LIGANDS #Chemistry, Inorganic & Nuclear |
Tipo |
article original article publishedVersion |