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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Expanded ligands: bis( 2,2 ': 6 ',2 ''-terpyridine carboxylic acid) ruthenium(II) complexes as metallosupramolecular analogues of dicarboxylic acids
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Expanded ligands: bis( 2,2 ': 6 ',2 ''-terpyridine carboxylic acid) ruthenium(II) complexes as metallosupramolecular analogues of dicarboxylic acids

机译:扩展的配体:双(2,2':6',2'-叔吡啶羧酸)钌(II)配合物,作为二羧酸的金属超分子类似物

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摘要

Ligands in which multiple metal-binding domains are linked by a metal-containing moiety rather than a conventional organic group are described as "expanded ligands". The use of 4,4'-difunctionalised {Ru(tpy)(2)} units provides a linear spacer between metal-binding domains and we have extended this motif to expanded ligands containing two carboxylic acid metal-binding domains. In this paper, we describe the synthesis and structural characterisation of ruthenium(II) complexes of 2,2': 6', 2"-terpyridine-4'-carboxylic acid and 4'-carboxyphenyl-2,2': 6', 2"-terpyridine. The ability of the ruthenium( II) centre to charge compensate deprotonation of the carboxylic acid leads to Zwitterionic complexes and three representative compounds have been structurally characterised.
机译:其中多个金属结合域通过含金属的部分而不是常规有机基团连接的配体被描述为“扩展的配体”。 4,4'-双官能化的{Ru(tpy)(2)}单元的使用在金属结合域之间提供了一个线性间隔基,我们已经将该基序扩展到了包含两个羧酸金属结合域的扩展配体。在本文中,我们描述了2,2':6',2“-吡啶4'-羧酸和4'-羧基苯基-2,2':6'的钌(II)配合物的合成和结构表征, 2”-叔吡啶。钌(II)中心对羧酸进行电荷补偿去质子化的能力导致两性离子络合物,并且在结构上表征了三种代表性化合物。

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