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首页> 外文期刊>Chemistry Letters >Introduction of Three Aryl Groups to Benzotriazinyl Radical by Suzuki-Miyaura Cross-coupling Reaction
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Introduction of Three Aryl Groups to Benzotriazinyl Radical by Suzuki-Miyaura Cross-coupling Reaction

机译:铃木-宫浦交叉偶联反应在苯并三嗪基自由基中引入三个芳基

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摘要

A new radical, 7-phenyl-1,3-bis(4-biphenylyi)-1,4-dihydro-1,2,4-benzotriazin-4-yl (2), was prepared from the iodo group-substituted benzotriazinyl radical 1 with phenyltriolborate salt by the Suzuki-Miyaura cross-coupling reaction at room temperature. An X-ray crystal structural analysis clarified its crystal structure. ESR measurements and DFT calculations revealed that its unpaired electron was more delocalized over the molecule than that of Blatter's radical due to the substituent effect.
机译:由碘基取代的苯并三嗪基自由基制备了一个新的自由基7-苯基-1,3-双(4-联苯基)-1,4-二氢-1,2,4-苯并三嗪-4-基(2) 1在室温下通过Suzuki-Miyaura交叉偶联反应与苯三硼硼酸盐反应。 X射线晶体结构分析明确了其晶体结构。 ESR测量和DFT计算表明,由于取代基效应,其不成对的电子在分子上的位置比Blatter的基团更大。

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