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铼(III)、(IV)和(V)的吡唑基甲烷配合物的合成与结构

Syntheses and structures of pyrazolylmethane complexes of rhenium(III), (IV) and (V).

作者信息

Cowley Andrew R, Dilworth Jonathan R, Salichou Maria

机构信息

Central Chemistry Department, University of Oxford, 12 Mansfield Road, Oxford, UK.

出版信息

Dalton Trans. 2007 Apr 28(16):1621-9. doi: 10.1039/b617549j. Epub 2007 Mar 6.

Abstract

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.

摘要

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。

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