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Diboron complexes of binucleating bis(amidinate) ligands

机译:双核双(酰胺基)配体的Diboron配合物

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The synthesis and X-ray crystal structures of the following bis(amidinate)-substituted boron halides are reported: 1,3-C6H4[C{N(SiMe3)}(2)BCl2](2) (3), 1,4-C6H4[C{N(SiMe3)}(2)BCl2](2) (4), 1,4-C6H4[C{N(SiMe3)}(2)B(Ph)Cl](2) (5), 1,4-C6H4[C{NCy}(2)BCl2](2) (6), and 1,4C(6)H(4)[C6H4C{NCy}(2)B(Ph)Cl](2) (7). Compounds 3-5 were prepared by trimethylsilyl chloride elimination, while 6 and 7 were prepared via salt metathesis reactions of the appropriate dilithiurn bis(amidinates) with BCl3 or PhBCl2. The molecular structures of complexes 3, 5, and 6 were determined by single-crystal X-ray diffraction, along with that of the free bis(amidine) 1a. (c) 2006 Elsevier B.V. All rights reserved.
机译:报告了以下双(ami酰胺基)取代的卤化硼的合成和X射线晶体结构:1,3-C6H4 [C {N(SiMe3)}(2)BCl2](2)(3),1,4 -C6H4 [C {N(SiMe3)}(2)BCl2](2)(4),1,4-C6H4 [C {N(SiMe3)}(2)B(Ph)Cl](2)(5) ,1,4-C6H4 [C {NCy}(2)BCl2](2)(6)和1,4C(6)H(4)[C6H4C {NCy}(2)B(Ph)Cl](2 )(7)。通过消除三甲基甲硅烷基氯来制备化合物3-5,而通过适当的二锂双(酰胺基)与BCl3或PhBCl2的盐复分解反应来制备化合物6和7。配合物3、5和6的分子结构是通过单晶X射线衍射确定的,以及游离的双(am)1a的分子结构是确定的。 (c)2006 Elsevier B.V.保留所有权利。

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