首页> 外文期刊>European journal of inorganic chemistry >Organoamido- and Aryloxo-Lanthanoids, 19 Synthesis and Structures of cisoid and transoid Bis(1,2-dimethoxyethane)bis(#eta#~2-pyrazolato)lanthanoid(II) Complexes
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Organoamido- and Aryloxo-Lanthanoids, 19 Synthesis and Structures of cisoid and transoid Bis(1,2-dimethoxyethane)bis(#eta#~2-pyrazolato)lanthanoid(II) Complexes

机译:有机酰胺基和芳氧基-类胡兰类化合物,19顺式和反式双(1,2-二甲氧基乙烷)双(#eta#〜2-吡唑并合)镧系元素(II)的合成与结构

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The complexes [Yb(bind)_2(DME)_2], [Yb(MePhpz)_2(DME)_2], [Yb(azin)_2(DME)_2], and [Eu(Ph_2pz)_2(DME__2] (bindH = 4,5-dihydro-2H-benz[g]indazole; MePhpzH = 3-methyl-5-phenylpyrazole; azinH = 7-azaindole; Ph_2pzH = 3,5-diphenylpyrazole; DME = 1,2-dimethoxyethane) have been prepared by redox transmetallation between ytterbium or europium metal and the corresponding thallium(I) pyrazolate in tetrahydrofuran (THF) in the presence of mercury metal, followed by work up with DME. The thallium reagents were obtained by treatment of the appropriate pyrazole with thallium(I) ethoxide. Both [Yb(Ph_2pz)_2(DME)_2] and [Sm(Ph_2pz)_2(DME)_2] have been prepared by metathesis from LnI_2(THF)_2 and K(Ph_2pz) in THF, whilst the former has also been obtained by redox transmetallation from [Hg(Ph_2pz)_2] and ytterbium metal and by reaction of 3,5-diphenylpyrazole with Yb(C_6F_5)_2, and the latter from protolysis of [Sm{N(SiMe_3)_2}_2(THF)_2] with Ph_2pzH, followed in each case by crystallisation of the crude product from DME. Europium(II) 3,5-di-tert-butylpyrazolate was synthesised by a redox transmetallation/ligand exchange reaction between europium metal chunks, diphenylmercury(II), and 3,5-di-tert-butylpyrazole (tBu_2pzH) in the presence of mercury metal in THF, and [Eu(tBu_2pzH)_2(DME)_2] was isolated on crystallisation of the crude product from DME. The X-ray crystal structures of [Ln(L)_2(DME)_2] (Ln=Yb, L = bind or azin; Ln = Eu or Sm, L = Ph_2pz; Ln = Eu, L = tBu_2pz), each of a different crystallographic form, reveal eight-coordinate lanthanoid complexes with two #eta#~2-pyrazolate and two chelating DME ligands, but the structures differ in the relationship (cisoid or transoid) between the pyrazolate ligands. Thus cen-Ln-cne (cen = centre of the N-N bond) angles of 106.7 deg [Yb(bind)_2(DME)_2] (3a), 141.4 deg [Yb(azin)_2(DME)_2] (3c), 142.2 deg [Eu(Ph_2pz)_2(DME)_2] (4a), 107.4 deg [Eu(tBu_2pz)_2(DME)_2] (4b), and 102.1 deg [Sm(Ph_2pz)_2(DME)_2] (5) are observed.
机译:络合物[Yb(bind)_2(DME)_2],[Yb(MePhpz)_2(DME)_2],[Yb(azin)_2(DME)_2]和[Eu(Ph_2pz)_2(DME__2)(bindH = 4,5-二氢-2H-苯并[g]吲唑; MePhpzH = 3-甲基-5-苯基吡唑; azinH = 7-氮杂吲哚; Ph_2pzH = 3,5-二苯基吡唑; DME = 1,2-二甲氧基乙烷)在金属汞存在下,通过在四氢呋喃(THF)中metal或euro金属与相应的吡唑late(I)吡唑化物之间进行氧化还原金属转移,然后用DME处理。by试剂通过用appropriate(I)处理适当的吡唑而制得[Yb(Ph_2pz)_2(DME)_2]和[Sm(Ph_2pz)_2(DME)_2]都是由THF中的LnI_2(THF)_2和K(Ph_2pz)复分解制备的,而前者具有也可以通过[Hg(Ph_2pz)_2]和metal金属的氧化还原金属转移,以及3,5-二苯基吡唑与Yb(C_6F_5)_2的反应而获得,后者是通过[Sm {N(SiMe_3)_2} _2()的蛋白水解而获得的。 THF)_2]与Ph_2pzH,然后在每种情况下结晶结晶DME的产品。 ,(II)3,5-二叔丁基吡唑酸酯是通过of金属块,二苯基汞(II)和3,5-二叔丁基吡唑(tBu_2pzH)之间的氧化还原金属转移/配体交换反应合成的从DME中粗产物结晶后分离出[Eu(tBu_2pzH)_2(DME)_2]和[Eu(tBu_2pzH)_2(DME)_2]。 [Ln(L)_2(DME)_2]的X射线晶体结构(Ln = Yb,L =结合或azin; Ln = Eu或Sm,L = Ph_2pz; Ln = Eu,L = tBu_2pz),每个一种不同的晶体形式,揭示了具有两个#eta#〜2-吡唑酸酯和两个螯合DME配体的八坐标镧系元素配合物,但吡唑酸酯配体之间的关系(顺式或反式)结构不同。因此,cen-Ln-cne(cen = NN键的中心)角度为106.7度[Yb(bind)_2(DME)_2](3a),141.4度[Yb(azin)_2(DME)_2](3c) ,142.2度[Eu(Ph_2pz)_2(DME)_2](4a),107.4度[Eu(tBu_2pz)_2(DME)_2](4b)和102.1度[Sm(Ph_2pz)_2(DME)_2]( 5)观察。

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