36472-83-0Relevant articles and documents
[{ReN(Me2PhP)(Et2dtc)Cl}2{ReN(Et 2dtc)2}2{SbCl3}2] - A novel tetranuclear rhenium complex with asymmetric nitrido bridges
Stelzer,Hagenbach,Abram
, p. 703 - 706 (2002)
The reaction of [ReN(Et2dtc)2(Me2PhP)] (Me2PhP = dimethylphenylphosphine, Et2dtc- = diethyldithiocarbamate) with SbCl3 in dichloromethane results in the formation of [{ReN(Me2PhP)(Et2dtc)Cl}2{ReN(Et 2dtc)2}2{SbCl3}2]. A {Re≡N-}4 ring with asymmetric nitrido bridges is stabilised by the co-ordination of SbCl3 onto the chloro ligands and sulphur atoms of the dithiocarbamates. The compound decomposes upon heating in acetonitrile and the fragments of the tetrameric complex re-arrange to form [ReN(Me2PhP)(Et2dtc)Cl]4 and [ReN(Et2dtc)2]. The multinuclear rhenium compounds have been studied by X-ray crystallography. The 8-membered {Re≡N-}4 ring system in [{ReN(Me2PhP)(Et2dtc)Cl}2{ReN(Et 2dtc)2}2{SbCl3}2] is almost planar, while that of [ReN(Me2PhP)(Et2dtc)Cl]4 is clearly V-shaped when viewed down either diagonal Re...Re axis. A dihedral angle of 47.88(2)° has been found between the contributing planes.
Nitrido-technetium and -rhenium Complexes with Chelating Phosphines: Synthesis, Reactivity and Crystal Structures
Marchi, Andrea,Marvelli, Lorenza,Rossi, Roberto,Magon, Luciano,Uccelli, Licia,et al.
, p. 1281 - 1286 (2007/10/02)
Nitrido-technetium(V) and -rhenium(V) complexes of general formula 1), 1,8-bis(diphenylphosphino)-3,6-dioxaoctane (L2) or 1,1,1-tris(diphenylphosphinomethyl)ethane (L3)> have been synthesized and characterized.They were prepared by the reduction of VINCl4>(1-) or by the replacement of the two triphenylphosphines of (M = Re or Tc) by bidentate or tripodal polyphosphine ligands L.Reaction of these complexes with an excess of potassium O-ethyl dithiocarbonate yields neutral dithiocarbonate compounds , while cationic and neutral complexes (1+) and were obtained upon reaction with K(S2CNEt2).The crystal structures of 1> and 2> have been determined by X-ray crystallography; the complex 1> shows square-pyramidal coordination at technetium with the Tc atom displaced from the basal plane towards the N atom by 0.410 Angstroem.An unusual trigonal-bipyramidal geometry is observed for 2>.The TcN bond distances (1.60 Angstroem) in both complexes are indicative of a strong triple bond.