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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Highly selective extraction of Cu(II) and Zn(II) using [B(3-iPrpz)(4)](-) (iPrpz = isopropylpyrazolyl)
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Highly selective extraction of Cu(II) and Zn(II) using [B(3-iPrpz)(4)](-) (iPrpz = isopropylpyrazolyl)

机译:使用[B(3-iPrpz)(4)](-)(iPrpz =异丙基吡唑基)高度选择性地萃取Cu(II)和Zn(II)

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摘要

The solvent extraction of first-series transition metal ions {n(II), Fe(II), Co(II), Ni(II), Cu(II) and Zn(Il)}with [B(3-iPrpz)4](-)(iPrpz = isopropylpyrazolyl) is reported. Although the previously reported tetrakis(pyrazolyl)borates, [B(PZ)(4)](-) and [B(3-Mepz)(4)](-), quantitatively extracted all the studied transition metal ions, [B(3-iPrpZ)(4)](-) extracted only Cu(II) and Zn(II). In order to elucidate the origin of the selectivity, the structures of the extracted species, [B(3-iPrPZ)(4)](2)Zn (1) and [B(3-iPrpZ)(4)]Cu(OCOCH3) (2), were determined by single-crystal X-ray diffraction. Complex 1 has a tetrahedral geometry with each ligand having bidentate coordination. Complex 2 has a distorted square pyramidal geometry with [B(3-iPrpz)(4)](-) having tridentate coordination and the acetate anion having asymmetric bidentate coordination. These structures of the extracted species are different from those of the previously studied tetrakis(pyrazolyl)borates, which are octahedral A(2)M with each ligand having tridentate coordination (A(-) = tetrakis(pyrazolyl)borate, M2+ = first-series transition metal ion). Because the bulky isopropyl groups at the 3-position of the pyrazolyl ring prevent octahedral geometry, the other metal ions cannot form stable and extractable complexes with [B(3-iPrpZ)(4)](-). (C) 2003 Elsevier Ltd. All rights reserved.
机译:[B(3-iPrpz)4]萃取第一系列过渡金属离子{n(II),Fe(II),Co(II),Ni(II),Cu(II)和Zn(II)}的溶剂报道了](-)(iPrpz =异丙基吡唑基)。尽管先前报道的四(吡唑基)硼酸酯[B(PZ)(4)](-)和[B(3-Mepz)(4)](-)定量提取了所有研究的过渡金属离子[B( 3-iPrpZ)(4)](-)仅提取Cu(II)和Zn(II)。为了阐明选择性的起源,提取物的结构为[B(3-iPrPZ)(4)](2)Zn(1)和[B(3-iPrpZ)(4)] Cu(OCOCH3 )(2)通过单晶X射线衍射测定。配合物1具有四面体几何形状,每个配体具有二齿配位。配合物2具有扭曲的方形锥体几何形状,其中[B(3-iPrpz)(4)](-)具有三齿配位,乙酸根阴离子具有不对称的双齿配位。提取物种的这些结构与先前研究的四(吡唑基)硼酸酯的结构不同,后者是八面体A(2)M,每个配体具有三齿配位(A(-)=四(吡唑基)硼酸酯,M2 + =第一-系列过渡金属离子)。因为在吡唑基环的3位大的异丙基会阻止八面体的几何形状,所以其他金属离子无法与[B(3-iPrpZ)(4)](-)形成稳定且可萃取的络合物。 (C)2003 Elsevier Ltd.保留所有权利。

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