Planar and Bent BN-Embedded p-Quinodimethanes Synthesized by Transmetalation of Bis(trimethylsilyl)-1,4-dihydropyrazines with Chloroborane

Planar and Bent BN-Embedded p-Quinodimethanes Synthesized by Transmetalation of Bis(trimethylsilyl)-1,4-dihydropyrazines with Chloroborane
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双(三甲基硅基)-1,4-二氢吡嗪与氯硼烷的金属转移合成平面和弯曲BN嵌入的对醌二甲烷

DOI:
10.1021/acs.organomet.8b00294
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发表时间:
2018
期刊:
影响因子:
2.8
通讯作者:
Yamashita Makoto
Yamashita Makoto
中科院分区:
化学2区
文献类型:
--
作者:
Noguchi Mao;Suzuki Katsunori;Kobayashi Jun;Yurino Taiga;Tsurugi Hayato;Mashima Kazushi;Yamashita Makoto

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以双(三甲基硅基)-1,4-二氢吡嗪为无机盐还原剂,与9-氯-9-硼杂环己烯反应,合成了两种BN-嵌入对奎诺二甲烷衍生物。X-射线衍射仪分析了所得π共轭化合物的平面或弯曲结构。由于HOMO分布的不同,它们的光物理性质与其平面或弯曲结构有关。
Two BN-embeddedp-quinodimethane derivatives were synthesized by a reaction of bis(trimethylsilyl)-1,4-dihydropyrazines, which are known as inorganic-salt-free reductants, with 9-chloro-9-borafluorene. The planar or bent structures of the resulting π-conjugated compounds were revealed by X-ray diffraction analysis. Their photophysical properties relate to their planar or bent structures due to the difference in the distribution of the HOMO.
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