首页> 美国卫生研究院文献>Acta Crystallographica Section E: Crystallographic Communications >Tetra­kis(μ-4-tert-butyl­benzoato)-κ3 O:OO′;κ3 OO′:O′;κ4 O:O′-bis­aqua­bis­(4-tert-butyl­benzoato-κ2 OO′)(4-tert-butyl­benzoic acid-κO)praseodymium(III)
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Tetra­kis(μ-4-tert-butyl­benzoato)-κ3 O:OO′;κ3 OO′:O′;κ4 O:O′-bis­aqua­bis­(4-tert-butyl­benzoato-κ2 OO′)(4-tert-butyl­benzoic acid-κO)praseodymium(III)

机译:Tetrakis(μ-4-叔丁基苯并)-κ3 O:OO′;κ3 OO:O;κ4 O:O-bis aquabis(4-叔丁基苯并-κ2 OO)(4-叔丁基苯甲酸-κO)ody(III)

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摘要

The reaction of praseodymium nitrate and 4-tert-butyl­benzoic acid (tBBAH) in aqueous solution yielded the dinuclear title complex, [Pr2(C11H13O2)6(C11H14O2)2(H2O)2], which has non-crystallographic Ci symmetry. The two PrIII ions are linked by two bridging and two bridging–chelating tBBA ligands, with a Pr⋯Pr separation of 4.0817 (9) Å. Each PrIII ion is nine-coordinated by one chelating tBBA ion, one monodentate tBBAH ligand and one water mol­ecule in a distorted tricapped trigonal–prismatic environment. The complex mol­ecules are linked into infinite chains along the c axis by inter­molecular O—H⋯O hydrogen bonds.
机译:硝酸与4-叔丁基­苯甲酸(tBBAH)在水溶液中反应生成双核标题化合物[Pr2(C11H13O2)6(C11H14O2)2(H2O)2],具有非晶体Ci对称性。这两个Pr III 离子通过两个桥接和两个桥接螯合的tBBA配体连接,Pr aPr分离度为4.0817(9)Å。每个Pr III 离子在扭曲的三棱柱棱柱形棱柱形环境中被一个螯合的tBBA离子,一个单齿的tBBAH配体和一个水分子九配位。复杂分子通过分子间OH-H = O氢键沿c轴连接成无限链。

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