4.8 Article

Azaboradibenzo[6]helicene: Carrier Inversion Induced by Helical Homochirality

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 48, 页码 19600-19603

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja310372f

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资金

  1. PRESTO Program of JST
  2. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [23685020]
  3. NEXT Program of the Japan Society for the Promotion of Science (JSPS)
  4. Asahi Glass Foundation
  5. Grants-in-Aid for Scientific Research [23685020, 11J03688] Funding Source: KAKEN

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Azaboradibenzo[6]helicene, a new semiconductor material possessing helical chirality, has been synthesized via a tandem bora-Friedel Crafts-type reaction. Unprecedented carrier inversion between the racemate (displaying p-type semiconductivity) and the single enantiomer (displaying n-type semiconductivity) was observed and can be explained by changes in the molecular packing induced by helical homochirality.

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