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首页> 外文期刊>Russian Journal of Coordination Chemistry >Phenyltellurenyl Halide Complexes of Ruthenium and Rhenium (CO)2RuBr2(PhTeBr)2 and (CO)3Re(PhTeI)3(μ~3-I): Synthesis and Crystal and Molecular Structures
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Phenyltellurenyl Halide Complexes of Ruthenium and Rhenium (CO)2RuBr2(PhTeBr)2 and (CO)3Re(PhTeI)3(μ~3-I): Synthesis and Crystal and Molecular Structures

机译:钌和hen的苯基碲烯基卤化物(CO)2RuBr2(PhTeBr)2和(CO)3Re(PhTeI)3(μ〜3-I):合成及晶体和分子结构

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摘要

Reactions of Ru3(CO)_(12) with PhTeBr3 and of Re(CO)5Cl with PhTel in benzene give the stable complexes (CO)2RuBr2(PhTeBr)2 (I) and (CO)3Re(PhTeI)3(μ~3-I) (II) containing two and three ligands PhTeX (X = Br or I), respectively. The bonds between these ligands and the central metal atom are fairly shortened (on average, Ru-Te, 2.608 A; Re-Te, 2.7554(12)-2.7634(13) A). The Te-X bonds in the ligands PhTeBr (2.5163(5) A) and PhTel (2.7893(15) A) are not lengthened appreciably. In complex II, the iodide anion is not coordinated by rhenium, yet being attached through weak secondary bonds to three Te atoms of the three ligands PhTel.
机译:Ru3(CO)_(12)与PhTeBr3的反应以及Re(CO)5Cl与PhTel在苯中的反应得到稳定的络合物(CO)2RuBr2(PhTeBr)2(I)和(CO)3Re(PhTeI)3(μ〜 3-I)(II)分别包含两个和三个配体PhTeX(X = Br或I)。这些配体和中心金属原子之间的键相当短(平均Ru-Te为2.608 A; Re-Te为2.7554(12)-2.7634(13)A)。配体PhTeBr(2.5163(5)A)和PhTel(2.7893(15)A)中的Te-X键没有明显延长。在络合物II中,碘化物阴离子不被coordinate配位,而是通过弱的次级键连接到三个配体PhTel的三个Te原子上。

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