Browsing by Author "Elipe, S"

Now showing 1 - 2 of 2
  • No Thumbnail Available
    Item
    Bis(diphenylphosphino)amine and their dichalcogenide derivatives as ligands in rhodium(III), iridium(III), and ruthenium(II) complexes.: Crystal structures of [(η5-C5Me5)MCl{η2-(SePPh2)2N}] (M = Rh, Ir)
    (2000) Valderrama, M; Contreras, R; Lamata, MP; Viguri, F; Carmona, D; Lahoz, FJ; Elipe, S; Oro, LA
    Reaction of the dimers [{(eta(5)-C5Me5)MCl}(2)(mu-Cl)(2)] (M = Rh, Ir) or [{(eta(6)-arene)RuCl}(2)(mu-Cl)(2)] (arene = p-(MeC6H4Pr)-Pr-i, C6Me6) with NH(PPh2)(2) in the presence of AgA (A = BF4, PF6) leads to the mononuclear cationic complexes [(eta(5)-C5Me5)MCl{eta(2)- (PPh2)(2)NH}]A (M = Rh (1), Ir (2)) or [(eta(6)-arene)RuCl{eta(2)-(PPh2)(2)NH}]A (arene = p-(MeC6H4Pr)-Pr-i (3), C6Me6 (4)). Similar reactions using the chalcogenide derivatives NH(EPPh2)(2) (E = S, Se) yield the neutral complexes [(eta(5)-C5Me5)RhCl{eta(2)-(EPPh2)(2)N}] (E = S (5), Se (6)), [(eta(5)-C5Me5)IrCl{eta(2)-(EPPh2)(2)N}] (E = S (7), Se (8)), [(eta(6)-arene)RuCl{eta(2)-(SPPh2)(2)N}] (arene = C6H6 (9), p-(MeC6H4Pr)-Pr-i (10)) and [(eta(6)-arene)RuCl{eta(2)-(SePPh2)(2)N)}] (arene = C6Me6 (11), p-(MeC6H4Pr)-Pr-i (12)). Chloride abstraction from complexes 5-8 with AgPF6 in the presence of PPh3 gives the cationic complexes [(eta(5)-C5Me5)Rh{eta(2)-(EPPh2)(2)N}(PPh3)]PF6 (E = S (13), Se (14)) and [(eta(5)-C5Me5)Ir{eta(2)-(EPPh2)(2)N}(PPh3)]PF6 (E = S (15), Se (16)). Complexes 13-16 can also be synthesised from the starting dinuclear complexes, AgPF6, NH(EPPh2)(2) and PPh3. Using this alternative synthetic route the related ruthenium complexes [(eta(6)-C6Me6)Ru{eta(2)-(EPPh2)(2)N}(C5H5N)] BF4 (E = S (17), Se (18)) can be prepared. All described compounds have been characterised by microanalysis and NMR (H-1, P-31) and IR spectroscopy. The crystal structures of the neutral complexes [(eta(5)-C5Me5)MCl{eta(2)-(SePPh2)(2)N}] (M = Rh (6), Ir (8)) have been determined by X-ray diffraction methods. Both complexes exhibit analogous pseudo-octahedral molecular structures with a C5Me5 group occupying three coordination positions and a bidentate chelate Se,Se'-bonded ligand and a chloride atom completing the coordination sphere. (C) 2000 Elsevier Science S.A. All rights reserved.
  • No Thumbnail Available
    Item
    Synthesis of transition-metal complexes with heterodifunctional ligands derived of NH(PPh2)2.: Crystal structure of [(η5-C5Me5)RhCl{η2-P, Se-Ph2PNP(Se)Ph2}]•CH2Cl2
    (2001) Valderrama, M; Contreras, R; Muñoz, P; Lamata, MP; Carmona, D; Lahoz, FJ; Elipe, S; Oro, LA
    The uncoordinated P atom of the bis(diphenylphosphine)amine (dppa) ligand in complexes [(ring)MCl2(eta (1)-P-PPh2NHPPh2)] (M = Rh, Ir. Ru) reacts with sulphur or selenium to form [(ring)MCl2(eta (1)-P-PPh2-NHP(E)Ph-2)] (E = S (1-3), Se (4-6)) containing the P-coordinated monosulphide or monoselenide ligands. The selenium derivatives have also been directly prepared from the corresponding [{(ring)MCl2)(2)] dimer and dppaSe. Chloride abstraction from rhodium and ruthenium complexes gives the neutral compounds [(ring)MCl(eta (2)-P,E-PPh2NP(E)Ph-2)] (7-10) whilst the iridium derivatives yield cationic complexes of the general formula [{eta (5)-C5Me5)IrCl(eta (2)-P,E-PPh2NHP(E)Ph-2)](+) (11 and 12). The crystal structure of complex [(eta (5)-C5Me5)RhCl{eta (2)-P,SePPh2NP(Se)Ph-2}] has been established by X-ray crystallography. The rhodium atom exhibits a distorted octahedral coordination with a eta (5)-C5Me5 group occupying the centre of three octahedral sites, a bidentate chelate P,Se-bonded ligand and a chloride atom complete the metal coordination sphere. (C) 2001 Elsevier Science B.V. All rights reserved.