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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >A new C-anionic tripodal ligand 2-{bis(benzothiazolyl)(methoxy)methyl}phenyl and its bismuth complexes
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A new C-anionic tripodal ligand 2-{bis(benzothiazolyl)(methoxy)methyl}phenyl and its bismuth complexes

机译:一种新的C-Anionic三架子配体2- {双(苯并噻唑基)(甲氧基)甲基}苯基及其铋配合物

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摘要

A new tripodal C-anionic ligand, 2-{bis(benzothiazolyl)(methoxy)methyl}phenyl (L), was stably generated by the reaction of the ligand precursor (L '), the corresponding bromide (2-BrC6H4)(MeO)C(C7H4NS)(2) (C7H4NS = 2-benzothiazolyl), with nBuLi at -104 degrees C in the presence of TMEDA (N,N,N ',N '-tetramethylethylenediamine). The ligand lithium salt reacted with BiCl3 to give a 2 : 1 complex L2BiCl. A 1 : 1 complex LBiCl2 was obtained in good yield by the redistribution reaction between L2BiCl and BiCl3. X-ray diffraction analysis revealed that the ligand L coordinated in an expected kappa(3)-C,N,N ' coordination mode in LBiCl2, while it coordinated in kappa(3)-C,N,O and kappa(2)-C,O coordination modes in L2BiCl. The ligand precursor reacted with BiX3 (X = Cl, Br) to give 1 : 1 complexes L ' BiX3 and was found to act as a neutral tripodal C(pi),N,N-ligand.
机译:在TMEDA(N,N,N',N'-四甲基乙二胺)存在下,通过配体前体(L')、相应的溴(2-BrC6H4)(MeO)C(C7H4NS)(2)(C7H4NS=2-苯并噻唑基)与nBuLi在-104℃下反应,稳定地生成了一种新的三脚架C-阴离子配体2-{双(苯并噻唑基)(甲氧基)甲基}苯基(L)。配体锂盐与BiCl3反应生成2:1络合物L2BiCl。通过L2BiCl与BiCl3的再分配反应,得到了产率较高的1:1络合物LBiCl2。X射线衍射分析表明,配体L在LBiCl2中以预期的kappa(3)-C,N,N'配位模式配位,而在L2Bil2中以kappa(3)-C,N,O和kappa(2)-C,O配位模式配位。配体前体与BiX3(X=Cl,Br)反应生成1:1配合物L’BiX3,并被发现作为中性三脚架C(pi),N,N-配体。

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