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首页> 外文期刊>Organic letters >Functionalized Carbon Nanohoops: Synthesis and Structure of a [9]Cycloparaphenylene Bearing Three 5,8-Dimethoxynaphth-1,4-diyl Units
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Functionalized Carbon Nanohoops: Synthesis and Structure of a [9]Cycloparaphenylene Bearing Three 5,8-Dimethoxynaphth-1,4-diyl Units

机译:功能化的碳纳米环:合成和结构的[9]环对亚苯基带有三个5,8-二甲氧基萘-1,4-二基单元

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摘要

A functionalized [9]cycloparaphenylene ([9]CPP) bearing three evenly spaced 5,8-dimethoxynaphth-1,4-diyl units and two macrocyclic [6]CPP precursors have been synthesized. The Diels?Alder reaction between (E,E)-1,4-bis(4-bromophenyl)-1,3-butadiene and 1,4-benzoquinone followed by methylation produces cis-5,8-bis(4-bromophenyl)-5,8-dihydro-1,4-dimethoxynaphthalene as the key intermediate for the construction of the hooplike structures. The nickelmediated homocoupling reactions followed by aromatization led to the functionalized [9]CPP.
机译:合成了带有三个均匀间隔的5,8-二甲氧基萘-1,4-二基单元和两个大环[6] CPP前体的功能化[9]环对亚苯基([9] CPP)。 (E,E)-1,4-双(4-溴苯基)-1,3-丁二烯与1,4-苯醌之间的狄尔斯-阿尔德反应,然后甲基化生成顺5,8-双(4-溴苯基) -5,8-二氢-1,4-二甲氧基萘是构建环状结构的关键中间体。镍介导的均偶联反应,然后进行芳构化,导致官能化的[9] CPP。

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