Cowley Andrew R, Dilworth Jonathan R, Salichou Maria
Central Chemistry Department, University of Oxford, 12 Mansfield Road, Oxford, UK.
Dalton Trans. 2007 Apr 28(16):1621-9. doi: 10.1039/b617549j. Epub 2007 Mar 6.
Reaction of [ReOCl3(PPh3)(2)] with HCpz(3) (pz = pyrazole) in dichloromethane leads to the formation of a new Re(iv) complex [ReCl3(HCpz3)]X (X=Cl, [ReO4]) with loss of the rhenium-oxo group. We also report a convenient, high-yield synthetic route to complexes of the type ReOXn(L)+ (X=Cl, Br, n = 2, 3) by the reaction of bis(pyrazolylmethane) and bis(pyrazolylacetate) ligands with [ReOCl3(PPh3)2]. Dinuclear complexes containing the O=Re-O-Re=O group were also isolated and structurally characterised. We have also investigated the reactions of these ligands with diazenide precursors and isolated and characterised complexes of the type [ReClx(N2Ph) (L)(PPh3)] (x = 1,2). The potential applications of these complexes as radiopharmaeuticals is discussed.
在二氯甲烷中,[ReOCl₃(PPh₃)₂]与HCpz₃(pz = 吡唑)反应,导致形成一种新的铼(IV)配合物[ReCl₃(HCpz₃)]X(X = Cl,[ReO₄]),同时失去铼-氧基团。我们还报道了一种便捷、高产率的合成路线,通过双(吡唑基甲烷)和双(吡唑基乙酸酯)配体与[ReOCl₃(PPh₃)₂]反应,合成[ReOXₙ(L)](3 - n)+类型的配合物(X = Cl,Br,n = 2,3)。还分离并对含有O=Re-O-Re=O基团的双核配合物进行了结构表征。我们还研究了这些配体与重氮化物前体的反应,并分离并表征了[ReClₓ(N₂Ph)(L)(PPh₃)]类型的配合物(x = 1,2)。讨论了这些配合物作为放射性药物的潜在应用。