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首页> 外文期刊>Journal of Organometallic Chemistry >Carbaborane-functionalised 2,2 ': 6 ',2 ''-terpyridine ligands for metallosupramolecular chemistry: Syntheses, complex formation, and the crystal and molecular structures of 4 '-(optho-carboranyl)-2,2 ': 6 ',2 ''-terpyridine and 4 '-(ortho-carboranyl
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Carbaborane-functionalised 2,2 ': 6 ',2 ''-terpyridine ligands for metallosupramolecular chemistry: Syntheses, complex formation, and the crystal and molecular structures of 4 '-(optho-carboranyl)-2,2 ': 6 ',2 ''-terpyridine and 4 '-(ortho-carboranyl

机译:碳硼烷官能化的2,2':6',2'-吡啶吡啶配体用于金属超分子化学:合成,络合物形成以及4'-(邻-甲碳烷基)-2,2':6'的晶体和分子结构, 2''-叔吡啶和4'-(邻氨基甲酰基

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摘要

A series of functionalised 2,2':6',2 "-terpyridine ligands, each with a closo-1,2-C2B10H10R (R = H or (SiBuMe2)-Bu-t) substituent in the 4' position, either directly or indirectly attached to the heterocyclic ring, has been prepared; two members of the series, 4'-(3-ortho-carboranylpropoxy)-2,2':6',2 "-terpyridine (4) and 4'-(ortho-carboranyl)-2,2':6',2 "-terpyridine (7) have been characterised by X-ray crystallography. The reaction of ligand (7) with alcohols results in the boron decapping of the close-cage and yields a Zwitter-ionic nido-cluster-functionalised ligand. Analogous changes to the carbaborane cage have been observed in complexes in which the terpyridine domain is coordinated to ruthenium(II). However, decapping does not occur if a (SiBuMe2)-Bu-t-protected carbaborane cage is incorporated into the terpyridine ligands. (C) 1998 Elsevier Science S.A. [References: 30]
机译:一系列功能化的2,2':6',2''-吡啶吡啶配体,每个配体在4'位置直接有closo-1,2-C2B10H10R(R = H或(SiBuMe2)-Bu-t)取代基已制备或间接连接到杂环上;该系列的两个成员,4'-(3-邻-甲氧烷基丙氧基)-2,2':6',2“-吡啶(4)和4'-(邻-碳硼烷基)-2,2':6',2“-吡啶(7)已通过X射线晶体学表征。配体(7)与醇的反应导致密闭笼罩的硼解封并生成a两性离子型氮簇功能化配体,在其中吡啶环结构域与钌(II)配位的配合物中,发现了碳甲环的类似变化,但是如果(SiBuMe2)-Bu-t- (C)1998 Elsevier Science SA [参考:30]

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