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Naphthalene derivatives peri-substituted by Group 13 elements

机译:被13族元素取代的萘衍生物

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This review focuses on the chemistry of naphthalene derivatives substituted by Group 13 moieties at the peri-positions. Depending on the nature of the Group 13 elements, different synthetic approaches have been considered. 1,8-Diborylated naphthalene complexes are conveniently prepared by metathesis of boron halides or alkoxides with 1,8-dilithionaphthulene. Such complexes can also be obtained by ring opening reaction of 1,8-boron bridged naphthalene species. Owing to the proximity of the boryl moieties, these derivatives are often sterically congested. Gallium and indium derivatives have also been prepared. In this case, however, alternative synthetic approaches have been used. These derivatives can be obtained by reaction of GaCl_3 or InCl_3 with 1,8-bis(trimethylstannyl)naphthalene. The transmetalation reaction of indium(Ⅰ) halides with 1,8-bis(halomercurio)naphthalene has also proved useful for the synthesis of naphthalenediylindium complexes. While the development of various applications is still being explored, the 1,8-diborylated naphthalene complexes serve as bidendate Lewis acidic hosts for neutral and anionic guests. Recently, such complexes have also served to provide a scaffold for the formation of radicals that feature intramolecular one-electron σ-bonds.
机译:这篇综述着重于在周边位置被第13族部分取代的萘衍生物的化学性质。根据第13组元素的性质,已经考虑了不同的合成方法。通过将卤化硼或醇盐与1,8-二锂邻萘并蒽复分解,可方便地制备1,8-二甲酰化萘络合物。这样的配合物也可以通过1,8-硼桥联的萘物种的开环反应获得。由于硼基部分的接近,这些衍生物经常在空间上是拥塞的。还制备了镓和铟衍生物。然而,在这种情况下,已经使用了替代的合成方法。这些衍生物可以通过GaCl_3或InCl_3与1,8-双(三甲基锡烷基)萘反应而获得。卤化铟(Ⅰ)与1,8-双(卤代curio)萘的金属转移反应也已证明可用于合成萘二亚乙基配合物。尽管仍在探索各种应用的开发,但1,8-二硼化萘络合物可作为中性和阴离子客体的双侧路易斯酸性主体。近来,此类络合物还已经提供了用于形成具有分子内单电子σ键特征的自由基的支架。

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