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Di(benzothiazol-2-yl)phosphanide as a Janus-head ligand to caesium

机译:DI(苯并噻唑-2-基)磷酸作为Janus-Head配体到铯

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摘要

Starting from tris(benzothiazol-2-yl)phosphane (1) an advanced Janus-head ligand, di(benzothiazol-2yl)phosphane (2), was synthesised and structurally characterised. The heteroaryl substituents of this ligand provide both hard and soft donor sites. Surprisingly, the phosphorus atom in 2 is divalent and the hydrogen atom is directly bonded to one ring nitrogen atom and hydrogen bonded to the second. Compound 2 decomposes in any common solvent other than diethyl ether and a new preparation to improve the yields of 2 is presented. A coordination polymer, [(Cs(bth)(2)P}(8)] (3) (bth=benzothiazol-2-yl), was obtained when the sec-phosphane 2 was allowed to react with elemental caesium in a 1:1 ratio in diethyl ether at -78 degrees C. In 3 each anion is coordinated to four caesium cations and vice versa. The central phosphorus atom is coordinated to two metal atoms above and below the mean plane of the anion in positions in which the two lone pairs of a four-electron donor are anticipated. Two additional cations R-bridge both ring nitrogen atoms. Hence both faces of the Janus-head ligand are coordinated to the same number of metal cations but in a different way.
机译:从TRI开始(苯并噻唑-2-基)磷酸(1)先进的Janus-head配体,在结构和结构表征中合成和结构表征。该配体的杂芳基取代基提供了硬质和软供体部位。令人惊讶的是,2中的磷原子是二价,氢原子直接键合到一个环氮原子并氢键合到第二个环氮原子和氢气。化合物2在除乙醚以外的任何常见溶剂中分解,并提出了新的制剂以提高2的产率。当允许仲膦2与1份元素铯反应时,获得配位聚合物[(Cs(Bth)(2)P}(8)](3)(Bth =苯并噻唑-2-基) :1在-78℃的乙醚中的比乙醚的比例在3中,每个阴离子配位为四个铯阳离子,反之亦然。中央磷原子与上方的两个金属原子配位,在其中的阴离子的平均平均平均平均平面之下协调预期两个孤立的四电子供体。两个额外的阳离子R桥两个环氮原子。因此,Janus-head配体的两个面部配位与相同数量的金属阳离子,但以不同的方式协调。

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